# HG changeset patch
# User nathandunn
# Date 1466971228 14400
# Node ID 850bb90bd66788348ddebd745fcd60707f1e5c52
planemo upload commit b529f45bf9fecbac1457a65b6b81e3b95200fced
diff -r 000000000000 -r 850bb90bd667 LICENSE
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/LICENSE Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,27 @@
+Copyright (c) 2016, Nathan Dunn
+All rights reserved.
+
+Redistribution and use in source and binary forms, with or without
+modification, are permitted provided that the following conditions are met:
+
+* Redistributions of source code must retain the above copyright notice, this
+ list of conditions and the following disclaimer.
+
+* Redistributions in binary form must reproduce the above copyright notice,
+ this list of conditions and the following disclaimer in the documentation
+ and/or other materials provided with the distribution.
+
+* Neither the name of galaxy-monarch-curl nor the names of its
+ contributors may be used to endorse or promote products derived from
+ this software without specific prior written permission.
+
+THIS SOFTWARE IS PROVIDED BY THE COPYRIGHT HOLDERS AND CONTRIBUTORS "AS IS"
+AND ANY EXPRESS OR IMPLIED WARRANTIES, INCLUDING, BUT NOT LIMITED TO, THE
+IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE ARE
+DISCLAIMED. IN NO EVENT SHALL THE COPYRIGHT HOLDER OR CONTRIBUTORS BE LIABLE
+FOR ANY DIRECT, INDIRECT, INCIDENTAL, SPECIAL, EXEMPLARY, OR CONSEQUENTIAL
+DAMAGES (INCLUDING, BUT NOT LIMITED TO, PROCUREMENT OF SUBSTITUTE GOODS OR
+SERVICES; LOSS OF USE, DATA, OR PROFITS; OR BUSINESS INTERRUPTION) HOWEVER
+CAUSED AND ON ANY THEORY OF LIABILITY, WHETHER IN CONTRACT, STRICT LIABILITY,
+OR TORT (INCLUDING NEGLIGENCE OR OTHERWISE) ARISING IN ANY WAY OUT OF THE USE
+OF THIS SOFTWARE, EVEN IF ADVISED OF THE POSSIBILITY OF SUCH DAMAGE.
diff -r 000000000000 -r 850bb90bd667 README.rst
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/README.rst Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,11 @@
+
+
+This project wraps the Gene Ontology SOLR services (GOLR) exposed by the [Monarch initiative](https://monarchinitiative.org).
+
+# Gene Ontology Curl
+
+ planemo serve
+
+
+
+
diff -r 000000000000 -r 850bb90bd667 arguments.png
Binary file arguments.png has changed
diff -r 000000000000 -r 850bb90bd667 create_shed.sh
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/create_shed.sh Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,5 @@
+planemo shed_init --name=geneontology \
+ --owner=nathandunn \
+ --description="Enriches Related biological data using ontology driven data." \
+ --long_description="Tool Suite that Pulls related Variants, Phenotypes, Diseases, Genes, and Homologes" \
+ --category="Web Services"
diff -r 000000000000 -r 850bb90bd667 demo.png
Binary file demo.png has changed
diff -r 000000000000 -r 850bb90bd667 monarch-genes-for-diseases.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/monarch-genes-for-diseases.xml Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,67 @@
+
+
+
+
+
+ $output1
+ ]]>
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ doi:10.1038/nprot.2015.124
+
+
diff -r 000000000000 -r 850bb90bd667 monarch-genes-for-phenotypes.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/monarch-genes-for-phenotypes.xml Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,57 @@
+
+
+
+
+
+ $output1
+ ]]>
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ doi:10.1038/nprot.2015.124
+
+
diff -r 000000000000 -r 850bb90bd667 monarch-homologues.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/monarch-homologues.xml Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,57 @@
+
+
+
+
+
+ $output1
+ ]]>
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ doi:10.1038/nprot.2015.124
+
+
diff -r 000000000000 -r 850bb90bd667 monarch-phenopackets.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/monarch-phenopackets.xml Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,72 @@
+
+
+
+
+
+ $output1
+ ]]>
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ doi:10.1038/nprot.2015.124
+
+
diff -r 000000000000 -r 850bb90bd667 monarch-phenotypes-for-disease.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/monarch-phenotypes-for-disease.xml Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,57 @@
+
+
+
+
+
+ $output1
+ ]]>
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ doi:10.1038/nprot.2015.124
+
+
diff -r 000000000000 -r 850bb90bd667 monarch-variants-for-diseases.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/monarch-variants-for-diseases.xml Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,57 @@
+
+
+
+
+
+ $output1
+ ]]>
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ doi:10.1038/nprot.2015.124
+
+
diff -r 000000000000 -r 850bb90bd667 monarch-variants-for-phenotypes.xml
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/monarch-variants-for-phenotypes.xml Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,58 @@
+
+
+
+
+
+ $output1
+ ]]>
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+
+ doi:10.1038/nprot.2015.124
+
+
diff -r 000000000000 -r 850bb90bd667 requirements.txt
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/requirements.txt Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,1 @@
+planemo
diff -r 000000000000 -r 850bb90bd667 test-data/2-diseases-overlap.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/2-diseases-overlap.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,1 @@
+DOID:14330,OMIM:168600
diff -r 000000000000 -r 850bb90bd667 test-data/2-diseases.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/2-diseases.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,1 @@
+DOID:14330,OMIM:607426
diff -r 000000000000 -r 850bb90bd667 test-data/2-genes.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/2-genes.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,1 @@
+NCBIGene:11132,NCBIGene:84290
\ No newline at end of file
diff -r 000000000000 -r 850bb90bd667 test-data/2-phenotypes.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/2-phenotypes.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,1 @@
+HP:0000739,MP:0001363
\ No newline at end of file
diff -r 000000000000 -r 850bb90bd667 test-data/disease.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/disease.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,1 @@
+DOID:14330
diff -r 000000000000 -r 850bb90bd667 test-data/empty.tsv
diff -r 000000000000 -r 850bb90bd667 test-data/gene.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/gene.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,1 @@
+NCBIGene:11132
\ No newline at end of file
diff -r 000000000000 -r 850bb90bd667 test-data/genes-for-2-diseases-intersection.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/genes-for-2-diseases-intersection.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,23 @@
+NCBIGene:4729 NDUFV2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:6315 ATXN8OS NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:2747 GLUD2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4287 ATXN3 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:203228 chromosome 9 open reading frame 72 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:6311 ATXN2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:26281 fibroblast growth factor 20 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4929 NR4A2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:126 ADH1C NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6908 TATA-box binding protein NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1621 dopamine beta-hydroxylase (dopamine beta-monooxygenase) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:627 BDNF NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4535 ND1 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:23317 DNAJC13 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:1815 dopamine receptor D4 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:9627 synuclein alpha interacting protein NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:497258 BDNF-AS NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:2629 GBA NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
diff -r 000000000000 -r 850bb90bd667 test-data/genes-for-2-diseases-union.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/genes-for-2-diseases-union.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,130 @@
+NCBIGene:37853 Mlp60A NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:39002 Prm NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:627 BDNF NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3630 insulin NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2944 GSTM1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17449559 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:33824 Gpdh NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens OMIM:260540 Parkinson-Dementia Syndrome ECO:0000220|ECO:0000322 sequencing assay evidence|imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4729 NDUFV2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1565 CYP2D6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:15174030|PMID:14991823 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3482 insulin like growth factor 2 receptor NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4842 nitric oxide synthase 1 (neuronal) NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:26383258 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5243 ATP binding cassette subfamily B member 1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20558393 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:15882845|PMID:19946270|PMID:25149416|PMID:22043175|PMID:16573651|PMID:12588799|PMID:22841634|PMID:24582596|PMID:15198987|PMID:17010972|PMID:23628791 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4129 MAOB NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:43497 Obp99b NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens Orphanet:240112 Progressive supranuclear palsy - progressive non fluent aphasia ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:31826 rdgA NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19915575|PMID:23628791|PMID:25149416|PMID:23017109|PMID:20205471|PMID:22043175|PMID:23472874|PMID:19915576|PMID:17388990 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2244 FGB NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23233872 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6315 ATXN8OS NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:260300 autosomal recessive early-onset Parkinson disease 15 ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:2670 glial fibrillary acidic protein NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:3569 interleukin 6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4128 MAOA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17449559 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2747 GLUD2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4803 nerve growth factor (beta polypeptide) NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:199 AIF1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:168601 autosomal dominant Parkinson disease 1 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4287 ATXN3 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:203228 chromosome 9 open reading frame 72 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:4566 TRNK NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:6531 solute carrier family 6 (neurotransmitter transporter), member 3 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16112329|PMID:19590691|PMID:16963468|PMID:9763484 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6311 ATXN2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:53564 retinin NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:26281 fibroblast growth factor 20 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2203 FBP1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens OMIM:613643 Parkinson Disease 5, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4217 mitogen-activated protein kinase kinase kinase 5 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21815648 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3077 HFE NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16824219 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:605543 Parkinson Disease 4, Autosomal Dominant ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens OMIM:607060 autosomal dominant Parkinson disease 8 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4929 NR4A2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:55532 SLC30A10 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3313 HSPA9 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16565515 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177|PMID:19915575 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:3643 INSR NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2950 glutathione S-transferase pi 1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17190945|PMID:23721876 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:27429 HTRA2 NCBITaxon:9606 Homo sapiens OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:23400 ATP13A2 NCBITaxon:9606 Homo sapiens OMIM:606693 Kufor-Rakeb syndrome ECO:0000033|ECO:0000220|ECO:0000322|ECO:0000220 traceable author statement|sequencing assay evidence|imported manually asserted information used in automatic assertion|sequencing assay evidence PMID:22768177|PMID:22022275|PMID:22847264 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1728 NQO1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17188257 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:126 ADH1C NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:55737 VPS35 retromer complex component NCBITaxon:9606 Homo sapiens OMIM:614203 Parkinson Disease 17 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23037695|PMID:20800516|PMID:17010972|PMID:25149416|PMID:20423725|PMID:22898350|PMID:22043175|PMID:23792957|PMID:15784737 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:26058 GRB10 interacting GYF protein 2 NCBITaxon:9606 Homo sapiens OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:38508 Cpr64Aa NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3162 HMOX1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20664293|PMID:12151787|PMID:22355530|PMID:17690948|PMID:25149416|PMID:12732244|PMID:21245015|PMID:25064009|PMID:11535288|PMID:18353766|PMID:22166454|PMID:20711177|PMID:17131421|PMID:12885775|PMID:18322262|PMID:21892157|PMID:22043175|PMID:22185909|PMID:15099020|PMID:14535945|PMID:19915575|PMID:18841091|PMID:19915576|PMID:22110584 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+MGI:1857323 Up NCBITaxon:10090 Mus musculus DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:43829 ATPsynbeta NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:32133 Hsc70-3 NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:23317 DNAJC13 NCBITaxon:9606 Homo sapiens OMIM:616361 Parkinson Disease 21 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:55737 VPS35 retromer complex component NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6908 TATA-box binding protein NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6202 RPS8 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1621 dopamine beta-hydroxylase (dopamine beta-monooxygenase) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4729 NDUFV2 NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:27429 HTRA2 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:683 BST1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19915576 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3480 insulin like growth factor 1 receptor NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:100129518 LOC100129518 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17188257|PMID:18353766|PMID:25279756 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6147 ribosomal protein L23a NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:627 BDNF NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4540 MT-ND5 NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4535 ND1 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:43690 chp NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:23317 DNAJC13 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:38418 kst NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4541 MT-ND6 NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:6531 solute carrier family 6 (neurotransmitter transporter), member 3 NCBITaxon:9606 Homo sapiens OMIM:613135 Parkinsonism-Dystonia, Infantile ECO:0000322|ECO:0000220 imported manually asserted information used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3481 IGF2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4576 TRNT NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:1815 dopamine receptor D4 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:39826 fax NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1571 CYP2E1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16510128 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:9829 DnaJ heat shock protein family (Hsp40) member C6 NCBITaxon:9606 Homo sapiens OMIM:615528 Parkinson Disease 19, Juvenile-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:9627 synuclein alpha interacting protein NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:2629 GBA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20947659|PMID:25064009 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:7124 tumor necrosis factor NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:9045 RPL14 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:33721 Rtnl1 NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens Orphanet:240094 Progressive supranuclear palsy - pure akinesia with gait freezing ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:497258 BDNF-AS NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4099 MAG NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:8867 SYNJ1 NCBITaxon:9606 Homo sapiens OMIM:615530 Parkinson Disease 20, Early-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:6128 ribosomal protein L6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4540 MT-ND5 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:1981 eukaryotic translation initiation factor 4 gamma, 1 NCBITaxon:9606 Homo sapiens OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:2629 GBA NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:8398 phospholipase A2 group VI NCBITaxon:9606 Homo sapiens OMIM:612953 Parkinson Disease 14, Autosomal Recessive ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6571 solute carrier family 18 (vesicular monoamine transporter), member 2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16112329 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:23400 ATP13A2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416|PMID:23628791 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:25793 F-box protein 7 NCBITaxon:9606 Homo sapiens OMIM:260300 autosomal recessive early-onset Parkinson disease 15 ECO:0000322|ECO:0000033|ECO:0000220 imported manually asserted information used in automatic assertion|traceable author statement|sequencing assay evidence PMID:25029497 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset ECO:0000033|ECO:0000220 traceable author statement|sequencing assay evidence PMID:24475098|PMID:21421046 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3122 HLA-DRA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2580 GAK NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 ECO:0000323 imported automatically asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:44643 Cnx99A NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2941 GSTA4 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16510128 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4541 MT-ND6 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:33883 Cpr NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:126 ADH1C NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4571 MT-TP NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens Orphanet:240103 Progressive supranuclear palsy - corticobasal syndrome ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:6888 TALDO1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23233872 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1906 endothelin 1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:38990 Cpr66D NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1356 ceruloplasmin (ferroxidase) NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19159062|PMID:25758665 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:54822 TRPM7 NCBITaxon:9606 Homo sapiens OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 ECO:0000220|ECO:0000323 sequencing assay evidence|imported automatically asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:22043175|PMID:17010972|PMID:25149416|PMID:21366594|PMID:24374061 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
diff -r 000000000000 -r 850bb90bd667 test-data/genes-for-2-diseases.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/genes-for-2-diseases.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,136 @@
+NCBIGene:37853 Mlp60A NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:39002 Prm NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:627 BDNF NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3630 insulin NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2944 GSTM1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17449559 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:33824 Gpdh NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens OMIM:260540 Parkinson-Dementia Syndrome ECO:0000220|ECO:0000322 sequencing assay evidence|imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4729 NDUFV2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1565 CYP2D6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:15174030|PMID:14991823 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3482 insulin like growth factor 2 receptor NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:27235 COQ2 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4842 nitric oxide synthase 1 (neuronal) NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:26383258 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5243 ATP binding cassette subfamily B member 1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20558393 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:15882845|PMID:19946270|PMID:25149416|PMID:22043175|PMID:16573651|PMID:12588799|PMID:22841634|PMID:24582596|PMID:15198987|PMID:17010972|PMID:23628791 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4129 MAOB NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:23590 PDSS1 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:43497 Obp99b NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens Orphanet:240112 Progressive supranuclear palsy - progressive non fluent aphasia ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:31826 rdgA NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19915575|PMID:23628791|PMID:25149416|PMID:23017109|PMID:20205471|PMID:22043175|PMID:23472874|PMID:19915576|PMID:17388990 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2244 FGB NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23233872 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6315 ATXN8OS NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:260300 autosomal recessive early-onset Parkinson disease 15 ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:2670 glial fibrillary acidic protein NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:57107 PDSS2 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:56997 ADCK3 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 ECO:0000033 traceable author statement PMID:18319072 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3569 interleukin 6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4128 MAOA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17449559 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:57017 coenzyme Q9 NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2747 GLUD2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4803 nerve growth factor (beta polypeptide) NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:199 AIF1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:168601 autosomal dominant Parkinson disease 1 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4287 ATXN3 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:203228 chromosome 9 open reading frame 72 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:4566 TRNK NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:6531 solute carrier family 6 (neurotransmitter transporter), member 3 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16112329|PMID:19590691|PMID:16963468|PMID:9763484 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6311 ATXN2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:53564 retinin NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:26281 fibroblast growth factor 20 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2203 FBP1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens OMIM:613643 Parkinson Disease 5, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4217 mitogen-activated protein kinase kinase kinase 5 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21815648 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3077 HFE NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16824219 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:605543 Parkinson Disease 4, Autosomal Dominant ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens OMIM:607060 autosomal dominant Parkinson disease 8 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4929 NR4A2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:55532 SLC30A10 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3313 HSPA9 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16565515 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177|PMID:19915575 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:3643 INSR NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2950 glutathione S-transferase pi 1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17190945|PMID:23721876 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:27429 HTRA2 NCBITaxon:9606 Homo sapiens OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:23400 ATP13A2 NCBITaxon:9606 Homo sapiens OMIM:606693 Kufor-Rakeb syndrome ECO:0000033|ECO:0000220|ECO:0000322|ECO:0000220 traceable author statement|sequencing assay evidence|imported manually asserted information used in automatic assertion|sequencing assay evidence PMID:22768177|PMID:22022275|PMID:22847264 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1728 NQO1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17188257 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:126 ADH1C NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:55737 VPS35 retromer complex component NCBITaxon:9606 Homo sapiens OMIM:614203 Parkinson Disease 17 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23037695|PMID:20800516|PMID:17010972|PMID:25149416|PMID:20423725|PMID:22898350|PMID:22043175|PMID:23792957|PMID:15784737 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:26058 GRB10 interacting GYF protein 2 NCBITaxon:9606 Homo sapiens OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:38508 Cpr64Aa NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3162 HMOX1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20664293|PMID:12151787|PMID:22355530|PMID:17690948|PMID:25149416|PMID:12732244|PMID:21245015|PMID:25064009|PMID:11535288|PMID:18353766|PMID:22166454|PMID:20711177|PMID:17131421|PMID:12885775|PMID:18322262|PMID:21892157|PMID:22043175|PMID:22185909|PMID:15099020|PMID:14535945|PMID:19915575|PMID:18841091|PMID:19915576|PMID:22110584 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+MGI:1857323 Up NCBITaxon:10090 Mus musculus DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:43829 ATPsynbeta NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:32133 Hsc70-3 NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:23317 DNAJC13 NCBITaxon:9606 Homo sapiens OMIM:616361 Parkinson Disease 21 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:55737 VPS35 retromer complex component NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6908 TATA-box binding protein NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6202 RPS8 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1621 dopamine beta-hydroxylase (dopamine beta-monooxygenase) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4729 NDUFV2 NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:27429 HTRA2 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:683 BST1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19915576 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3480 insulin like growth factor 1 receptor NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:100129518 LOC100129518 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17188257|PMID:18353766|PMID:25279756 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6147 ribosomal protein L23a NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:627 BDNF NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4540 MT-ND5 NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4535 ND1 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:43690 chp NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:23317 DNAJC13 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:38418 kst NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4541 MT-ND6 NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:6531 solute carrier family 6 (neurotransmitter transporter), member 3 NCBITaxon:9606 Homo sapiens OMIM:613135 Parkinsonism-Dystonia, Infantile ECO:0000322|ECO:0000220 imported manually asserted information used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3481 IGF2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4576 TRNT NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:1815 dopamine receptor D4 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:39826 fax NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1571 CYP2E1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16510128 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:9829 DnaJ heat shock protein family (Hsp40) member C6 NCBITaxon:9606 Homo sapiens OMIM:615528 Parkinson Disease 19, Juvenile-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:9627 synuclein alpha interacting protein NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:2629 GBA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20947659|PMID:25064009 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:7124 tumor necrosis factor NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:9045 RPL14 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:33721 Rtnl1 NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens Orphanet:240094 Progressive supranuclear palsy - pure akinesia with gait freezing ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:497258 BDNF-AS NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4099 MAG NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:8867 SYNJ1 NCBITaxon:9606 Homo sapiens OMIM:615530 Parkinson Disease 20, Early-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:6128 ribosomal protein L6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4540 MT-ND5 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:1981 eukaryotic translation initiation factor 4 gamma, 1 NCBITaxon:9606 Homo sapiens OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:2629 GBA NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:8398 phospholipase A2 group VI NCBITaxon:9606 Homo sapiens OMIM:612953 Parkinson Disease 14, Autosomal Recessive ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6571 solute carrier family 18 (vesicular monoamine transporter), member 2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16112329 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:23400 ATP13A2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416|PMID:23628791 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:25793 F-box protein 7 NCBITaxon:9606 Homo sapiens OMIM:260300 autosomal recessive early-onset Parkinson disease 15 ECO:0000322|ECO:0000033|ECO:0000220 imported manually asserted information used in automatic assertion|traceable author statement|sequencing assay evidence PMID:25029497 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset ECO:0000033|ECO:0000220 traceable author statement|sequencing assay evidence PMID:24475098|PMID:21421046 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3122 HLA-DRA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2580 GAK NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 ECO:0000323 imported automatically asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:44643 Cnx99A NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2941 GSTA4 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16510128 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4541 MT-ND6 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:33883 Cpr NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:126 ADH1C NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4571 MT-TP NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens Orphanet:240103 Progressive supranuclear palsy - corticobasal syndrome ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:6888 TALDO1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23233872 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1906 endothelin 1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:38990 Cpr66D NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1356 ceruloplasmin (ferroxidase) NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19159062|PMID:25758665 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:54840 aprataxin NCBITaxon:9606 Homo sapiens OMIM:607426 Coenzyme Q10 Deficiency, Primary, 1 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:54822 TRPM7 NCBITaxon:9606 Homo sapiens OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 ECO:0000220|ECO:0000323 sequencing assay evidence|imported automatically asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:22043175|PMID:17010972|PMID:25149416|PMID:21366594|PMID:24374061 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
diff -r 000000000000 -r 850bb90bd667 test-data/genes-for-2-phenotypes-intersection.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/genes-for-2-phenotypes-intersection.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,245 @@
+MGI:109178 Fgf13 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22726441 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1270850 Slc6a2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23580201 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1913894 Uba6 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23499007 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96918 Mas1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9565612 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95819 Grin1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19915563 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2143311 Bbs4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16794820 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:101922 Tnc NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16553788 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2441758 Gpr26 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21924326 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1922391 Rasd2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15199135 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95821 Grin2b NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20357110 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1916933 Emc10 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20562862|MGI:3510987 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:96559 Il6 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:16843000|PMID:12946594|PMID:19378383 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1096362 Nrxn2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:25423136 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1100881 Prss12 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:95394 Eno2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23487260 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1922459 Sv2c NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23458503 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2651811 Tph2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:18212115|PMID:18212115 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2443472 Atf7 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19893493 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1328355 Wfs1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19477223 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2443963 Cadps2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17380209 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1098264 Kif13a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23438369 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3607718 sau NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104963 Npy1r NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22084082 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2443075 Cpeb3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24155305 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1930016 Shank3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:24652766 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2152453 Gsk3a NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20357757 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1100494 Ercc6 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22174697 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95832 Grn NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17764761 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:101916 Fabp7 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16882015 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1858193 Folh1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16190866 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95623 Gabrg2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15850489 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99479 Cckbr NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12459512 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:94876 Ddc NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23275025 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95811 Gria4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20662939 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1861942 Gtf2ird1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22652393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2139279 Hrh3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15078574 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2664186 Npas4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18815592 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2442233 Arhgef9 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17690689 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:106217 Cacna1e NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:11854466 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99917 Slc1a3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:18832146 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2442233 Arhgef9 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:17690689 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2151070 Ophn1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:17728457 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5308748 Bhv31 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:4940633 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1338824 Rgs9 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24784230 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98932 Vim NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9888296 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:94862 Slc6a3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:12617953 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:351 APP NCBITaxon:9606 Homo sapiens MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:9302276 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1096392 Hcn1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:14651847 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96067 Htt NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23001568 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1097716 Arx NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:19605412|PMID:19605412 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99402 Adora2a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9262401 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1932872 Ctns NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:12370309 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:9445 integral membrane protein 2B NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20385796 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2444609 Nlgn3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:19360662|PMID:19360662 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1861437 Gsk3b NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20357757 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97441 Oprm1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22231481 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2441758 Gpr26 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:21924326 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1919764 Fgfbp3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20851768 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2685783 Baiap3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23698091 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1862037 Slc12a5 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15813942 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:107501 Kcnj11 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16530794 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2150393 Grin3b NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17880385 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:94876 Ddc NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23275025 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96668 Kcnc2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11124984 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1201690 Map6 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12231625 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96062 Hdc NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16412995|PMID:16310870 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96417 Ids NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16505002 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98366 Sox4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3064 huntingtin NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:19464370|PMID:20064390|PMID:20064390|PMID:24784230|PMID:19464370|PMID:19464370|PMID:24081492|PMID:24784230|PMID:19464370 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1913458 Nenf NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24058337 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1930016 Shank3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21423165 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97180 Mapt NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:20130183|PMID:22378884 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98742 Thra NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16131613 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96418 Idua NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18022143 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98493 Tbx1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:15084464|PMID:21908517|PMID:11239417|PMID:12413905 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:95622 Gabrd NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18667149 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1276123 Ucn NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:12091910 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1339468 S100a10 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16400147 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97362 Nos3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10964974 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88498 Crhr1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21885734 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96777 Lgals1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23118208 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88059 App NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:22336193|PMID:22336193|PMID:24278307 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:109392 Esr2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:8248223|PMID:15642619|PMID:9861029|PMID:11593044 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:5515451 M876b NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3613677 Shank1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18272690 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88106 Atp1a2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17234593 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1278315 Lrp5 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2143311 Bbs4 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16794820 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:109246 Htr4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000304 traceable author statement used in manual assertion PMID:14724239 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:114516 Glra3 NCBITaxon:10116 Rattus norvegicus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24430185 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1920211 Slc17a7 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17241289 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1328355 Wfs1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19477223 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:106038 Lrrn1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:5000289|PMID:20562862 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:2389173 Lrrtm1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:21818371 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1860139 Gabbr1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15321743|PMID:15706241 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2652818 Dcdc2a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21883923 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:892973 Gpr19 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:1890357 Igf2bp1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3609573 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3039563 Dlgap3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17713528 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:101784 Nes NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:23777740|PMID:20889973 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+MGI:94864 Dbh NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16723393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96217 Hprt NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24430185 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1861437 Gsk3b NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20357757 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1924933 Ehmt1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19896504 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97612 Plaur NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12533622 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97821 Pvalb NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24430185 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1101358 Npepps NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10407043 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98328 Sstr2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11029646 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1891433 Sppl3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20562862|PMID:20562862 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:101784 Nes NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23499007 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+MGI:95387 Emx1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22726441 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96928 Mc2r NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:2655403 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:103169 Scn8a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19737145 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6647 superoxide dismutase 1, soluble NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16737688 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96949 Mdk NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10096022 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:8878 sequestosome 1 NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23591541 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104628 Penk-rs NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:8849726 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96273 Htr1a NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:9844013 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95575 Fosb NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21679928 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97769 Prnp NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9117892|PMID:12742740|PMID:12742740 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:109392 Esr2 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:11593044 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88057 Apoe NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:15304509|PMID:12220566 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl|http://data.monarchinitiative.org/ttl/impc.ttl direct
+MGI:104628 Penk-rs NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:8849726 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97489 Pax5 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:23349049|PMID:23349049 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2137383 Csmd1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24244513 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:106644 Efna3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:25281279 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99918 Mecp2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:12160743|PMID:24283265 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96573 Ins2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17334640 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1355296 Park2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17883413 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:7415 VCP NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:20147319|PMID:20147319 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2135610 Dync1li1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21471385 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1298228 Foxq1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:16109771|PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104670 Fkbp5 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21935478 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99578 Drd1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:10884517|PMID:10884517 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1100498 Pitx3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20033184 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/impc.ttl inferred
+MGI:1352758 Ulk2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3609573 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:1889206 Skap2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24815314|PMID:16135797 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3039563 Dlgap3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:17713528 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1913869 Atat1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23748901 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:26598540 CLN6 NCBITaxon:9615 Canis lupus familiaris MP:0001363 increased anxiety-related response PMID:21234413 http://data.monarchinitiative.org/ttl/monarch.ttl|http://data.monarchinitiative.org/ttl/omia.ttl inferred
+MGI:2150016 Spred1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19118178 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99401 Adora1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11470917 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95634 Gad2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:10814732|PMID:10814732 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1921372 Tmem43 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20562862|MGI:3510987 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:87888 Chrna4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:11226318|PMID:10964949 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97374 Npy NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18616565 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1276123 Ucn NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12091910 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1098264 Kif13a NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23438369 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:103291 Rai1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:18285828|PMID:17517686|PMID:18285828|PMID:18285828 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:109583 Pten NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16675393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95808 Gria1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20699120 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2676665 Lrrc7 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22072671 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96273 Htr1a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:10751426|PMID:9844013|PMID:9844013|PMID:9724773|PMID:9724773|PMID:9826725|PMID:9826725|PMID:20152131 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:9445 integral membrane protein 2B NCBITaxon:9606 Homo sapiens MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20385796 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:18490011|PMID:24503275|PMID:24278307 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95667 Gbx1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24010020 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2679446 Slitrk1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18794888 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4204 MECP2 NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:22231481|PMID:22231481|PMID:22231481 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2449712 Fev NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20818386 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1270850 Slc6a2 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23580201 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97438 Oprd1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10835636 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:94925 Drd3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:10884517 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:103013 Cacna1c NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95832 Grn NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22062772 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1351636 Srr NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19065142 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2682328 Atmin NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20889973 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1921268 Als2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16107644|PMID:16107644 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:1096399 Vamp7 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22323709 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98331 Snap25 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:21949876|PMID:19043548 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:106677 Slc18a2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19553450 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:894312 Crhr2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:10742108|PMID:10742109|PMID:10742109 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99135 Xpa NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22174697 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+MGI:98331 Snap25 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:19043548|PMID:21949876 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2141866 Ric8a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16221497 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104726 Cplx2 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20412316 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1202722 Gtf2i NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20403157 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2386030 Gabbr2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15706241 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97360 Nos1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15158692 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:5663 presenilin 1 NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19936202 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88057 Apoe NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:15304509|PMID:10684907|PMID:15708438|PMID:15708438 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl|http://data.monarchinitiative.org/ttl/impc.ttl direct
+MGI:88256 Camk2a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:22084082|PMID:19420255|PMID:24503275 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+MGI:88059 App NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:17634375|PMID:8001115 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2179733 Mpst NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23759691 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1925031 Epm2aip1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24142699 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:108058 Adm NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18723674 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2449712 Fev NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:12546819|PMID:20818386 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1298228 Foxq1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96915 Maoa NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15272015 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104629 Penk NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11172058 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88145 Bdnf NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:17023662|PMID:11579207|PMID:17023662|PMID:20130183 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88497 Crhbp NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:10500222|PMID:10500222 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:1918639 Chd6 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20111866 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95583 Fshr NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:14502087 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:108067 Nkx2-1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17182767 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:109583 Pten NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16675393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1351641 Naglu NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10588735 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:1827 RCAN1 NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22511596 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2679448 Slitrk5 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20418887 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96721 L1cam NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:9580664 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:109483 Rnf103 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19753093|PMID:18958194|PMID:18958194 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:104735 Gt(ROSA)26Sor NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:18832146 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88495 Crem NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18562617 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99926 mt-Atp8 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19037013 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1351345 Grm8 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16045496 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95809 Gria2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:16216087|PMID:16099814 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1342774 Ppargc1a NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:15760270 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3064 huntingtin NCBITaxon:9606 Homo sapiens MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23001568 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1261791 Apba2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19420255 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1101358 Npepps NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:10407043 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1929864 Myg1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19818808 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1355296 Park2 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:17883413 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:108471 Ntan1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10805755 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104615 Cnr1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:12405999|PMID:15078564|PMID:11823890|PMID:23785142 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1932872 Ctns NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12370309 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1202717 Psen1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:22336193|PMID:24278307 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:351 APP NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:19936202|PMID:18184372|PMID:12742740|PMID:16876915|PMID:16289866|PMID:15016076 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104798 Tnf NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11063830 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1919835 Lypd1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19246390 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1927169 B4galt5 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3609573 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:95757 Slc2a3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18780771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2685783 Baiap3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23698091 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2137383 Csmd1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:24244513 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:2671987 Shank2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:22699619|PMID:22699620|PMID:22699619 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:107588 Gjb6 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12911759 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98824 Trhr NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17666589 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95564 Fmr1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19016890 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97384 Ntrk2 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:19158294|PMID:19158294|PMID:18832146|PMID:10571233 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:102707 Efna2 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:25281279 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88497 Crhbp NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10500222|PMID:10500222 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:88105 Atp1a1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3609573 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:2152453 Gsk3a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20357757 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:105089 Hsd17b4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:23777740|PMID:23777740 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96916 Maob NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15272015 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1929258 Kcnip3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19223600 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104510 Myo7a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:63673 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1861234 Wt NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:13834122 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1201414 Cer1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1277959 Dlg4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23268962 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98735 Th NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16723393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104735 Gt(ROSA)26Sor NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21885734 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95819 Grin1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19915563 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3584508 Kcnh5 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:95583 Fshr NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:14502087 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88470 Comt NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9707588 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1098271 Rgs2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11027316 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
diff -r 000000000000 -r 850bb90bd667 test-data/genes-for-2-phenotypes-union.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/genes-for-2-phenotypes-union.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,637 @@
+MGI:3589233 tmgc58 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence MGI:3053008|PMID:17629744 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:109178 Fgf13 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22726441 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1270850 Slc6a2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23580201 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1913894 Uba6 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23499007 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2156367 Tlr3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:20713712 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96918 Mas1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9565612 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:8131 NPRL3 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:23406172|PMID:17938043|PMID:9491171|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:95389 En1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:19679071 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:11132 CAPN10 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22397240|PMID:2209327|PMID:22188726|PMID:12429356 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:95819 Grin1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19915563 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6331 SCN5A NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:1759138|PMID:9172914|PMID:9602186|PMID:22796196|PMID:17854255 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:6391 succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000501 sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:2554 GABRA1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:11319492|PMID:21703932|PMID:21683658|PMID:19453714|PMID:21041102 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:97535 Pdyn NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:12843270 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88227 C3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:26400934 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:23671 TMEFF2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:25042611|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:5885 RAD21 cohesin complex component NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:19309268|PMID:18430761|PMID:17845236|PMID:17640042|PMID:19330433 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:10084 polyglutamine binding protein 1 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000501 sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:5290 phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000323 computational combinatorial evidence used in automatic assertion|imported automatically asserted information used in automatic assertion PMID:15857188|PMID:17587321|PMID:21883167|PMID:22773173|PMID:8539655 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:5078 PAX4 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:3117 HLA-DQA1 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000501 sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:5646419 Mbt2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence MGI:4940633 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:106593 Neurod6 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:21885734 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95808 Gria1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:15344919 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:22891 zinc finger protein 365 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:9484420|PMID:18571979|PMID:1759095|PMID:23228163|PMID:2225662 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2143311 Bbs4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16794820 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:101922 Tnc NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16553788 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2441758 Gpr26 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21924326 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1922391 Rasd2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15199135 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95821 Grin2b NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20357110 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:2645 glucokinase (hexokinase 4) NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1916933 Emc10 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20562862|MGI:3510987 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:96559 Il6 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:16843000|PMID:12946594|PMID:19378383 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:57491 aryl-hydrocarbon receptor repressor NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:20171652|PMID:12796866|PMID:7866213|PMID:20495477|PMID:21602797|PMID:10361400 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:4760 NEUROD1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1096362 Nrxn2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:25423136 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1100881 Prss12 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:95394 Eno2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23487260 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:720 C4A NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:17988328|PMID:14761134|PMID:22004346|PMID:15230354|PMID:19267789 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:3106 HLA-B NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:17988328|PMID:14761134|PMID:22004346|PMID:15230354|PMID:19267789 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1922459 Sv2c NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23458503 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2651811 Tph2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:18212115|PMID:18212115 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1353431 Pcsk1n NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:20367757 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2443472 Atf7 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19893493 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1328355 Wfs1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19477223 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1859216 Avpr1a NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:14647484|PMID:16046007 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2443963 Cadps2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17380209 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1347049 Clcn6 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:16950870 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1330290 Ovol1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000059|ECO:0000006 experimental phenotypic evidence|experimental evidence MGI:5576271 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/impc.ttl inferred
+MGI:101922 Tnc NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:16553788 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:94925 Drd3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:9402626|PMID:9402626|PMID:10884517 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1932544 Ndst3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:18385133 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1098264 Kif13a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23438369 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3607718 sau NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104963 Npy1r NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22084082 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96545 Il1r1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:19429130 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:109524 Trpc5 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:19450521|PMID:19450521 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3480 insulin like growth factor 1 receptor NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000304|ECO:0000220|ECO:0000322 traceable author statement used in manual assertion|sequencing assay evidence|imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2443075 Cpeb3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24155305 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1930016 Shank3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:24652766 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5646417 Mbt1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence MGI:4940633 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:64478 CUB and Sushi multiple domains 1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:24058526|PMID:17938043|PMID:9491171|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1928486 Tdo2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:19323847 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2152453 Gsk3a NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20357757 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1931838 Dbn1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000059 experimental phenotypic evidence http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/impc.ttl inferred
+NCBIGene:54600 UGT1A9 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:21425450|PMID:22558097 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:6899 TBX1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:15877762|PMID:20410726|PMID:22526976|PMID:22832905|PMID:21215459 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1100494 Ercc6 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22174697 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95832 Grn NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17764761 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:101916 Fabp7 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16882015 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6224 ribosomal protein S20 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:15857188|PMID:17587321|PMID:21883167|PMID:22773173|PMID:8539655 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:3651 pancreatic and duodenal homeobox 1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1858193 Folh1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16190866 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:2820 GPD2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:95623 Gabrg2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15850489 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88065 Araf NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:8805280|PMID:8805280 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99479 Cckbr NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12459512 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:94876 Ddc NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23275025 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95811 Gria4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20662939 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1861942 Gtf2ird1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22652393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1915541 Mto1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:25506927 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88495 Crem NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:10570204 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2139279 Hrh3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15078574 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2664186 Npas4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18815592 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:5663 presenilin 1 NCBITaxon:9606 Homo sapiens MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:16354928 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4292 mutL homolog 1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:22773173|PMID:8539655|PMID:15857188|PMID:21883167|PMID:17587321 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2442233 Arhgef9 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17690689 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5499183 Pedm29 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence MGI:4940633 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:106217 Cacna1e NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:11854466 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99917 Slc1a3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:18832146 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2442233 Arhgef9 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:17690689 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2151070 Ophn1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:17728457 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2151070 Ophn1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:17728457 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5308748 Bhv31 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:4940633 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:2157 F8 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:10734657|PMID:15357786|PMID:2378544|PMID:9302853|PMID:17498080 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:97610 Plat NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:15522965|PMID:12524546 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1100498 Pitx3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:20033184 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/impc.ttl inferred
+MGI:1338824 Rgs9 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24784230 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:351 APP NCBITaxon:9606 Homo sapiens MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:16236385|PMID:16354928|PMID:15016076|PMID:18931664|PMID:18931664|PMID:18931664|PMID:16236385 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98932 Vim NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9888296 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:54658 UGT1A1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:21425450|PMID:22558097 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:3611215 Wdup NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence MGI:3580105 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2441950 Adgrl3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:22575564 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1351340 Grm3 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:15619115 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88496 Crh NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:22231481 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:94862 Slc6a3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:12617953 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95574 Fos NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:1423615 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:351 APP NCBITaxon:9606 Homo sapiens MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:9302276 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4784 NFIX NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000322|ECO:0000304|ECO:0000220 imported manually asserted information used in automatic assertion|traceable author statement used in manual assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:6775 STAT4 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:17988328|PMID:14761134|PMID:22004346|PMID:15230354|PMID:19267789 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:104726 Cplx2 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:12915444 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1096392 Hcn1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:14651847 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2158015 Rln3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:21887138 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96067 Htt NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23001568 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1097716 Arx NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:19605412|PMID:19605412 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:8647 ATP binding cassette subfamily B member 11 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:24058526|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:99402 Adora2a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9262401 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6390 succinate dehydrogenase complex subunit B, iron sulfur (Ip) NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000501|ECO:0000220|ECO:0000220|ECO:0000246 evidence used in automatic assertion|sequencing assay evidence|sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:14605591|PMID:19569019|PMID:17474956|PMID:6829807|PMID:1576030 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:3145 hydroxymethylbilane synthase NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000322|ECO:0000501|ECO:0000220 imported manually asserted information used in automatic assertion|evidence used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:55869 histone deacetylase 8 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:19309268|PMID:17845236|PMID:17640042|PMID:18430761|PMID:19330433 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:9568 GABBR2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:7559318|PMID:15289208|PMID:1845224|PMID:2209418|PMID:20639284 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:3643278 Gpr52 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:24587241 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1932872 Ctns NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:12370309 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95564 Fmr1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:20011099|PMID:21220020|PMID:19016890|PMID:19016890 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1328360 Arid3a NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000059|ECO:0000006 experimental phenotypic evidence|experimental evidence MGI:5576271 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/impc.ttl inferred
+NCBIGene:9445 integral membrane protein 2B NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20385796 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2444609 Nlgn3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:19360662|PMID:19360662 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:108449 Adcyap1r1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:11483244 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1861437 Gsk3b NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20357757 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1920431 Nfatc4 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:16554754|PMID:16554754 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:87891 Chrnb2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:15541879 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+NCBIGene:6514 solute carrier family 2 (facilitated glucose transporter), member 2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:54657 UGT1A4 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:21425450|PMID:22558097 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:1181 chloride channel, voltage-sensitive 2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21703932|PMID:21683658|PMID:11319492|PMID:19453714|PMID:21041102 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2150150 Slc4a10 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:18165320 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97441 Oprm1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22231481 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2441758 Gpr26 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:21924326 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:54577 UGT1A7 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:21425450|PMID:22558097 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1919764 Fgfbp3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20851768 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2685783 Baiap3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23698091 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1862037 Slc12a5 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15813942 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:1524 CX3CR1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:169026 SLC30A8 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:107501 Kcnj11 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16530794 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:102724020 LOC102724020 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:24058526|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2150393 Grin3b NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17880385 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:94876 Ddc NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23275025 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96668 Kcnc2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11124984 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1201690 Map6 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12231625 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3811 KIR3DL1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:106644 Efna3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:25281279 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96062 Hdc NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16412995|PMID:16310870 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4149 MYC associated factor X NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:19569019|PMID:1576030|PMID:17474956|PMID:14605591|PMID:6829807 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:10644 insulin like growth factor 2 mRNA binding protein 2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:97808 Ptpra NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:12932834 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3119 HLA-DQB1 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000304|ECO:0000501|ECO:0000220 sequencing assay evidence|traceable author statement used in manual assertion|evidence used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:107501 Kcnj11 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:16530794 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:94924 Drd2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:11069937|PMID:11069937 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1261760 Lsamp NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:20888367 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1277202 Cnih1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:20562862|PMID:20562862 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:96417 Ids NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16505002 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98366 Sox4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3064 huntingtin NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:19464370|PMID:20064390|PMID:20064390|PMID:24784230|PMID:19464370|PMID:19464370|PMID:24081492|PMID:24784230|PMID:19464370 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1913458 Nenf NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24058337 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98869 Tuba1a NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:17218254|PMID:22101068 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:21698260|PMID:16877359|PMID:24503275 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1930016 Shank3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21423165 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97180 Mapt NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:20130183|PMID:22378884 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1924933 Ehmt1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:20005824|PMID:19896504 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:114798 SLITRK1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:8425124|PMID:20063404|PMID:8173824|PMID:1564054|PMID:23418216 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:98742 Thra NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16131613 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1278336 Cdkl5 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:23236174 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3458 IFNG NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:96418 Idua NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18022143 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3819691 Rgsc1770 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence MGI:3778963 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98493 Tbx1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:15084464|PMID:21908517|PMID:11239417|PMID:12413905 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+NCBIGene:6927 HNF1 homeobox A NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1277959 Dlg4 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:20952458 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95622 Gabrd NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18667149 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:109355 Stx1a NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:24136198 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:23171 glycerol-3-phosphate dehydrogenase 1-like NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17854255|PMID:1759138|PMID:9172914|PMID:9602186|PMID:22796196 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2685385 Kalrn NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:19020030|PMID:23116210 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1276123 Ucn NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:12091910 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1339468 S100a10 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16400147 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6356 CCL11 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:97362 Nos3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10964974 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99187 Zfp42 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000059 experimental evidence|experimental phenotypic evidence MGI:5576271 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/impc.ttl inferred
+NCBIGene:4204 MECP2 NCBITaxon:9606 Homo sapiens MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:15351775 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2441827 Rxfp3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:25257104 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4544 MTNR1B NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:4524 methylenetetrahydrofolate reductase (NAD(P)H) NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000246 computational combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:18700841|PMID:20495477|PMID:3817455|PMID:10361400|PMID:10734657|PMID:20171652|PMID:7875359|PMID:12796866|PMID:7866213|PMID:19187190 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:88498 Crhr1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21885734 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:5395 PMS2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:15857188|PMID:22773173|PMID:17587321|PMID:21883167|PMID:8539655 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:3643 INSR NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:96777 Lgals1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23118208 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88059 App NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:22336193|PMID:22336193|PMID:24278307 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:1548 CYP2A6 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:7559318|PMID:15289208|PMID:1845224|PMID:2209418|PMID:20639284 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:109392 Esr2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:8248223|PMID:15642619|PMID:9861029|PMID:11593044 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+NCBIGene:7097 TLR2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:6668935|PMID:6819753|PMID:7278143|PMID:1784156|PMID:7861049 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:5515451 M876b NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3613677 Shank1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18272690 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1915326 Dnajc9 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000059|ECO:0000059|ECO:0000006 experimental phenotypic evidence|experimental phenotypic evidence|experimental evidence MGI:5576271 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/impc.ttl inferred
+NCBIGene:116985 ARAP1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:25670933|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:5265 SERPINA1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000322|ECO:0000246 sequencing assay evidence|imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:23547634|PMID:18376109|PMID:19072562|PMID:9116423|PMID:3878661 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2447658 Disc1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:21903668 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88106 Atp1a2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17234593 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1278315 Lrp5 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:2642 GCGR NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:3039785 Syngap1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:23141534|PMID:23141534|PMID:19145222 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:1278 COL1A2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:21525520|PMID:21847749|PMID:75706|PMID:16137956|PMID:12099988 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2685918 Lpar5 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:23039190 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2143311 Bbs4 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16794820 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:87914 Aspa NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:21625469 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1261791 Apba2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:19420255 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:79734 potassium channel tetramerization domain containing 17 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000501 sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:109246 Htr4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000304 traceable author statement used in manual assertion PMID:14724239 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3073 HEXA NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:8355954|PMID:2739956|PMID:20597919|PMID:16301864|PMID:696935 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:25836 Nipped-B homolog (Drosophila) NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:19309268|PMID:17845236|PMID:17640042|PMID:18430761|PMID:19330433 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1923036 Ckap5 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:23936366 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:7040 TGFB1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246|ECO:0000220 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:20495477|PMID:10361400|PMID:20171652|PMID:12796866|PMID:7866213 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:97453 Oxt NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:12746288 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:799 calcitonin receptor NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:21525520|PMID:21847749|PMID:75706|PMID:16137956|PMID:12099988 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:2778 GNAS complex locus NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000501|ECO:0000220 evidence used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:114516 Glra3 NCBITaxon:10116 Rattus norvegicus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24430185 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:2212 FCGR2A NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:20171652|PMID:12796866|PMID:7866213|PMID:20495477|PMID:10361400 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1920211 Slc17a7 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17241289 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3043 HBB NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246|ECO:0000322 sequencing assay evidence|computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:21425450 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:6804 syntaxin 1A (brain) NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:20171652|PMID:12796866|PMID:7866213|PMID:20495477|PMID:10361400 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1328355 Wfs1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19477223 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3123 HLA-DRB1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:9484420|PMID:18571979|PMID:1759095|PMID:23228163|PMID:2225662 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:106038 Lrrn1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:5000289|PMID:20562862 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:2389173 Lrrtm1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:21818371 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1860139 Gabbr1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15321743|PMID:15706241 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96721 L1cam NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:14614101 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:56729 RETN NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2652818 Dcdc2a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21883923 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:11133 KPTN NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000322|ECO:0000501 sequencing assay evidence|imported manually asserted information used in automatic assertion|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1349461 B3galt2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+NCBIGene:2908 NR3C1 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000501|ECO:0000322 sequencing assay evidence|evidence used in automatic assertion|imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:8910 SGCE NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000501|ECO:0000220 evidence used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:892973 Gpr19 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+NCBIGene:2332 fragile X mental retardation 1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246|ECO:0000220 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:19429055|PMID:14994287|PMID:10972251|PMID:16176388|PMID:18297385 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:5646423 Tm47 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence MGI:4940633 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88296 Cacna1b NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:11350923 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6934 TCF7L2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22397240|PMID:2209327|PMID:22188726|PMID:12429356 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:1312 catechol-O-methyltransferase NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000177|ECO:0000220|ECO:0000501 genomic context evidence|sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1890357 Igf2bp1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3609573 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3045263 Dnajc5g NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000059|ECO:0000059 experimental evidence|experimental phenotypic evidence|experimental phenotypic evidence MGI:5576271 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/impc.ttl inferred
+MGI:3039563 Dlgap3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17713528 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:9569 GTF2I repeat domain containing 1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:12730029|PMID:21211940|PMID:22048961|PMID:21328569|PMID:22371147 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:186 angiotensin II receptor, type 2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:20171652|PMID:12796866|PMID:7866213|PMID:20495477|PMID:21602797|PMID:10361400 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:9479 mitogen-activated protein kinase 8 interacting protein 1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:2969 GTF2I NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:12730029|PMID:21211940|PMID:22048961|PMID:21328569|PMID:22371147 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1346858 Mapk1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:21849556 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1195461 Sept5 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:19240081 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97180 Mapt NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:17341679 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:7466 WFS1 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000322|ECO:0000220|ECO:0000501 imported manually asserted information used in automatic assertion|sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:149233 interleukin 23 receptor NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:17988328|PMID:14761134|PMID:22004346|PMID:15230354|PMID:19267789 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:101784 Nes NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:23777740|PMID:20889973 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+MGI:94864 Dbh NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16723393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:5770 PTPN1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:4436 MSH2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:22773173|PMID:21883167|PMID:8539655|PMID:15857188|PMID:17587321 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:96217 Hprt NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24430185 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1861437 Gsk3b NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20357757 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:7099 TLR4 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:17988328|PMID:14761134|PMID:22004346|PMID:15230354|PMID:19267789 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:102463 Nfatc2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:16554754|PMID:16554754 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:5621 PRNP NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000304|ECO:0000322|ECO:0000501|ECO:0000220 sequencing assay evidence|traceable author statement used in manual assertion|imported manually asserted information used in automatic assertion|evidence used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:5521 protein phosphatase 2 regulatory subunit B, beta NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000501|ECO:0000220|ECO:0000322 evidence used in automatic assertion|sequencing assay evidence|imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:3595 interleukin 12 receptor, beta 2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000323|ECO:0000246 imported automatically asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:17988328|PMID:14761134|PMID:22004346|PMID:15230354|PMID:19267789 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:24503275 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000501 sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1924933 Ehmt1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19896504 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:5660 prosaposin NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:7554686|PMID:23510063|PMID:20635362|PMID:9333269|PMID:12581195 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:50617 ATP6V0A4 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:21326311|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1277959 Dlg4 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:20952458 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97612 Plaur NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12533622 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97821 Pvalb NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24430185 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6531 solute carrier family 6 (neurotransmitter transporter), member 3 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:7559318|PMID:15289208|PMID:1845224|PMID:2209418|PMID:20639284 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1101358 Npepps NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10407043 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:57480 PLEKHG1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:21425450|PMID:24058526 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:98328 Sstr2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11029646 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:8243 structural maintenance of chromosomes 1A NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:19309268|PMID:17845236|PMID:17640042|PMID:18430761|PMID:19330433 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1891433 Sppl3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20562862|PMID:20562862 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:99479 Cckbr NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:15325774|PMID:15013032 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:101784 Nes NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23499007 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+MGI:95387 Emx1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22726441 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96928 Mc2r NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:2655403 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:54659 UGT1A3 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:21425450|PMID:22558097 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:103169 Scn8a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19737145 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:101927854 LOC101927854 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:24058526|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:95712 Gpr83 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:23088626 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88107 Atp1a3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:22025725 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:9209 LRRFIP2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000323|ECO:0000246 imported automatically asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:15857188|PMID:17587321|PMID:21883167|PMID:22773173|PMID:8539655 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:6647 superoxide dismutase 1, soluble NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16737688 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96949 Mdk NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10096022 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1929864 Myg1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:19818808 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:8878 sequestosome 1 NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23591541 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104628 Penk-rs NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:8849726 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96273 Htr1a NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:9844013 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95575 Fosb NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21679928 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:101784 Nes NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:23622066|PMID:10471508 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+MGI:97769 Prnp NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9117892|PMID:12742740|PMID:12742740 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+NCBIGene:50632 CALY NCBITaxon:9606 Homo sapiens MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:18295356 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1100526 Nr2e1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:17953618 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:5167 ectonucleotide pyrophosphatase/phosphodiesterase 1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:4540 MT-ND5 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:109392 Esr2 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:11593044 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88057 Apoe NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:15304509|PMID:12220566 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl|http://data.monarchinitiative.org/ttl/impc.ttl direct
+MGI:104628 Penk-rs NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:8849726 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1194506 Serpini1 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:12837630 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97489 Pax5 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:23349049|PMID:23349049 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:5378 PMS1 homolog 1, mismatch repair system component NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:15857188|PMID:17587321|PMID:21883167|PMID:22773173|PMID:8539655 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2137383 Csmd1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24244513 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:2685104 Akap5 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:18711127 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4072 EPCAM NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:15857188|PMID:17587321|PMID:21883167|PMID:22773173|PMID:8539655 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:106644 Efna3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:25281279 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:51164 DCTN4 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:20171652|PMID:12796866|PMID:7866213|PMID:20495477|PMID:10361400 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:5159 PDGFRB NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000501 sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:99918 Mecp2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:12160743|PMID:24283265 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99918 Mecp2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:22119903|PMID:22119903|PMID:18321864|PMID:16467389|PMID:24352790 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+MGI:88537 Csk NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:22348736 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:57338 junctophilin 3 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000322|ECO:0000501|ECO:0000220 imported manually asserted information used in automatic assertion|evidence used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:96573 Ins2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17334640 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1355296 Park2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17883413 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1098266 Chl1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:12391163 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:2629 GBA NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:7554686|PMID:23510063|PMID:9333269|PMID:20635362|PMID:12581195 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:7415 VCP NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:20147319|PMID:20147319 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2135610 Dync1li1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21471385 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:54579 UGT1A5 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:21425450|PMID:22558097 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1298228 Foxq1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:16109771|PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104670 Fkbp5 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21935478 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99578 Drd1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:10884517|PMID:10884517 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1100498 Pitx3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20033184 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/impc.ttl inferred
+NCBIGene:30835 CD209 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1352758 Ulk2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3609573 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:1298228 Foxq1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6349 CCL3L1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1889206 Skap2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24815314|PMID:16135797 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:1341787 Trpv1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:17251423 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3786 KCNQ3 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21703932|PMID:21683658|PMID:11319492|PMID:19453714|PMID:21041102 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2180756 Mchr1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:15988472 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3039563 Dlgap3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:17713528 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2139279 Hrh3 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:12130692 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3586 IL10 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246|ECO:0000246|ECO:0000323 sequencing assay evidence|computational combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion|imported automatically asserted information used in automatic assertion PMID:12098612|PMID:17988328|PMID:14761134|PMID:22276472|PMID:19267789|PMID:22004346|PMID:15230354|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:54575 UGT1A10 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:21425450|PMID:22558097 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:97783 Psap NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:20015957 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:23230 VPS13A NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000322|ECO:0000220|ECO:0000501 imported manually asserted information used in automatic assertion|sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1913869 Atat1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23748901 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:26598540 CLN6 NCBITaxon:9615 Canis lupus familiaris MP:0001363 increased anxiety-related response PMID:21234413 http://data.monarchinitiative.org/ttl/monarch.ttl|http://data.monarchinitiative.org/ttl/omia.ttl inferred
+NCBIGene:5468 PPARG NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2150016 Spred1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19118178 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000501|ECO:0000220 evidence used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:103296 Nfatc3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:16554754 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99401 Adora1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11470917 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3566 interleukin 4 receptor NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:95634 Gad2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:10814732|PMID:10814732 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:657 bone morphogenetic protein receptor type IA NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:15857188|PMID:17587321|PMID:21883167|PMID:22773173|PMID:8539655 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1921372 Tmem43 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20562862|MGI:3510987 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:109521 Htr2a NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:16873667|PMID:16873667|PMID:16873667|PMID:16873667 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:387837 CLEC12B NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:24058526|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:4567 TRNL1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17854255|PMID:1759138|PMID:9172914|PMID:9602186|PMID:22796196 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:99779 Chrna7 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:15541879|PMID:10454356 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6392 succinate dehydrogenase complex subunit D, integral membrane protein NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000501|ECO:0000220|ECO:0000246|ECO:0000220 evidence used in automatic assertion|sequencing assay evidence|computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:14605591|PMID:19569019|PMID:17474956|PMID:6829807|PMID:1576030 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:367 AR NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:21801726|PMID:18775430|PMID:1635303|PMID:17132758|PMID:17707426 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:87888 Chrna4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:11226318|PMID:10964949 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97374 Npy NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18616565 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97281 Ncam1 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000059|ECO:0000059 experimental phenotypic evidence|experimental phenotypic evidence http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/impc.ttl inferred
+NCBIGene:54941 RNF125 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000501|ECO:0000220 evidence used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:5499180 Pedm15 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence MGI:4940633 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1276123 Ucn NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12091910 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1098264 Kif13a NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23438369 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4541 MT-ND6 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1351339 Grm2 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:15619115 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:103291 Rai1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:18285828|PMID:17517686|PMID:18285828|PMID:18285828 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+NCBIGene:478 ATP1A3 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000501|ECO:0000322|ECO:0000220 evidence used in automatic assertion|imported manually asserted information used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1927140 Git1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:19383529 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:109583 Pten NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16675393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96217 Hprt NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:25100603|PMID:25100603 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1341867 Mmp24 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:14741353 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1929183 Tsc1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:23250422 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95808 Gria1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20699120 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:7096 TLR1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:6668935|PMID:6819753|PMID:7278143|PMID:1784156|PMID:7861049 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2137586 Dtnbp1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:25677649 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1338917 S100a1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:17045663 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3159 HMGA1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2676665 Lrrc7 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22072671 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98474 Tac1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:12427862 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:109525 Trpc4 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:24599464 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96273 Htr1a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:10751426|PMID:9844013|PMID:9844013|PMID:9724773|PMID:9724773|PMID:9826725|PMID:9826725|PMID:20152131 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3569 interleukin 6 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:102707 Efna2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:25281279 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:64127 NOD2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000323|ECO:0000246 imported automatically asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:17988328|PMID:14761134|PMID:22004346|PMID:15230354|PMID:19267789 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:96285 Slc6a4 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:21814181 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:5155 PDGFB NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000501 sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:9445 integral membrane protein 2B NCBITaxon:9606 Homo sapiens MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20385796 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:18490011|PMID:24503275|PMID:24278307 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:2668 GDNF NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:19569019|PMID:1576030|PMID:17474956|PMID:14605591|PMID:6829807 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:5646415 Mbtr3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence MGI:4940633 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:54578 UGT1A6 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:21425450|PMID:22558097 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:7466 WFS1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:54901 CDKAL1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22397240|PMID:2209327|PMID:22188726|PMID:12429356 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2145264 Nhlrc1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:21882344 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:25255 Dyrk1a NCBITaxon:10116 Rattus norvegicus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:11555628 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:8878 sequestosome 1 NCBITaxon:9606 Homo sapiens MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:23591541 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95667 Gbx1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24010020 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2679446 Slitrk1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18794888 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4204 MECP2 NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:22231481|PMID:22231481|PMID:22231481 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2449712 Fev NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20818386 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1270850 Slc6a2 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23580201 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:337867 UBAC2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000323|ECO:0000246 imported automatically asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:17988328|PMID:14761134|PMID:22004346|PMID:15230354|PMID:19267789 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1346542 Bace1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:15987683|PMID:16354928|PMID:16354928|PMID:15987683 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97438 Oprd1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10835636 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:8660 insulin receptor substrate 2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:94925 Drd3 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:10884517 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:103013 Cacna1c NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88256 Camk2a NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:24503275 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+NCBIGene:7276 TTR NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:9987556|PMID:21961415|PMID:23283376|PMID:21636023|PMID:15736742 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:96285 Slc6a4 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:14625138|PMID:16873667 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3984 LIM domain kinase 1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:12730029|PMID:21211940|PMID:22048961|PMID:21328569|PMID:22371147 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:95832 Grn NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22062772 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6517 SLC2A4 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:55714 TENM3 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:24058526|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1351636 Srr NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19065142 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2682328 Atmin NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20889973 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:106677 Slc18a2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:21814181 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6547 SLC8A3 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:20171652|PMID:12796866|PMID:7866213|PMID:20495477|PMID:10361400|PMID:21602797 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1347049 Clcn6 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:16950870 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1921268 Als2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16107644|PMID:16107644 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:1096399 Vamp7 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22323709 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2448269 tmgc8 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence MGI:2448159 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98331 Snap25 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:21949876|PMID:19043548 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:106677 Slc18a2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19553450 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:50484 ribonucleotide reductase M2 B (TP53 inducible) NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000501 sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:5251 phosphate regulating endopeptidase homolog, X-linked NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:21326311|PMID:17938043|PMID:9491171|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:8572 PDLIM4 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:21525520|PMID:21847749|PMID:75706|PMID:16137956|PMID:12099988 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:55654 TMEM127 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:6829807|PMID:19569019|PMID:1576030|PMID:17474956|PMID:14605591 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:894312 Crhr2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:10742108|PMID:10742109|PMID:10742109 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4210 MEFV NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:17988328|PMID:14761134|PMID:22004346|PMID:15230354|PMID:19267789 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:7428 von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:6829807|PMID:19569019|PMID:1576030|PMID:17474956|PMID:14605591 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:2956 MSH6 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:15857188|PMID:22773173|PMID:17587321|PMID:21883167|PMID:8539655 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:1201 CLN3 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000304|ECO:0000220 traceable author statement used in manual assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:6833 ABCC8 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:95622 Gabrd NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:10536021 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:9126 structural maintenance of chromosomes 3 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:19309268|PMID:18430761|PMID:17845236|PMID:17640042|PMID:19330433 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:23095 KIF1B NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:19569019|PMID:1576030|PMID:17474956|PMID:14605591|PMID:6829807 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:2623 GATA binding protein 1 (globin transcription factor 1) NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:20629912|PMID:1829081|PMID:6462129|PMID:12354323|PMID:12014236 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:5646425 Mbtr2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence MGI:4940633 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96765 Ldlr NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:16236385 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:7461 CLIP2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:12730029|PMID:21211940|PMID:22048961|PMID:21328569|PMID:22371147 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:99135 Xpa NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22174697 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+MGI:1930016 Shank3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:24652766|PMID:24652766|PMID:24652766|PMID:24652766 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:773 CACNA1A NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000501|ECO:0000220 evidence used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:98331 Snap25 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:19043548|PMID:21949876 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96274 Htr1b NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000059|ECO:0000006|ECO:0000006|ECO:0000059 experimental phenotypic evidence|experimental evidence|experimental evidence|experimental phenotypic evidence PMID:8091214|PMID:10996411|MGI:5576271|PMID:9603521 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl|http://data.monarchinitiative.org/ttl/impc.ttl direct
+NCBIGene:7421 vitamin D (1,25- dihydroxyvitamin D3) receptor NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000306 computational combinatorial evidence used in automatic assertion|inference from background scientific knowledge used in manual assertion PMID:21525520|PMID:21847749|PMID:75706|PMID:16137956|PMID:12099988 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:105094 Adcyap1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:11687615 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:100873924 HLX-AS1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:21326311|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:97769 Prnp NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:19666958|PMID:19666958|PMID:19666958 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3592 interleukin 12A NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:17988328|PMID:14761134|PMID:22004346|PMID:15230354|PMID:19267789 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2141866 Ric8a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16221497 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104726 Cplx2 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20412316 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2448275 tmgc10 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence MGI:2448159 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1202722 Gtf2i NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20403157 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2386030 Gabbr2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15706241 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3119 HLA-DQB1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:9484420|PMID:18571979|PMID:1759095|PMID:23228163|PMID:2225662 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:97360 Nos1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15158692 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1352466 Nr2c2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:23622066 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:5979 RET NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:17474956|PMID:14605591|PMID:6829807|PMID:19569019|PMID:1576030 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:4204 MECP2 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000006|ECO:0000006|ECO:0000501|ECO:0000220 experimental evidence|experimental evidence|evidence used in automatic assertion|sequencing assay evidence PMID:22231481|PMID:22231481 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:95820 Grin2a NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:23201971|PMID:23201971 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:7915 ALDH5A1 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000501|ECO:0000322|ECO:0000220 evidence used in automatic assertion|imported manually asserted information used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:894663 Ext1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:22411800 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:5663 presenilin 1 NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19936202 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104771 Erbb4 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:22378872 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+MGI:88057 Apoe NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:15304509|PMID:10684907|PMID:15708438|PMID:15708438 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl|http://data.monarchinitiative.org/ttl/impc.ttl direct
+NCBIGene:9031 bromodomain adjacent to zinc finger domain 1B NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:12730029|PMID:21211940|PMID:22048961|PMID:21328569|PMID:22371147 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:50940 PDE11A NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000501 sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2136690 Cers1 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:23074226 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1341110 Adcy8 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:10864938 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88256 Camk2a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:22084082|PMID:19420255|PMID:24503275 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+MGI:88059 App NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:17634375|PMID:8001115 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:1080 cystic fibrosis transmembrane conductance regulator NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322|ECO:0000220|ECO:0000246 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion|sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:1564054|PMID:12796866|PMID:10361400|PMID:7866213|PMID:20063404|PMID:20495477|PMID:20171652|PMID:8173824|PMID:23418216|PMID:8425124 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2179733 Mpst NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23759691 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1926555 Mapk8ip2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:21048139 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1925031 Epm2aip1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24142699 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3577 CXCR1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:54576 UGT1A8 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:21425450|PMID:22558097 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:112476 PRRT2 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000220|ECO:0000501 sequencing assay evidence|sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+MGI:108058 Adm NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18723674 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2449712 Fev NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:12546819|PMID:20818386 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:2332 fragile X mental retardation 1 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000322|ECO:0000304 sequencing assay evidence|imported manually asserted information used in automatic assertion|traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2139279 Hrh3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:15078574 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88257 Camk2b NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:25127391|PMID:25127391 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:1277 COL1A1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:21525520|PMID:21847749|PMID:75706|PMID:16137956|PMID:12099988 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:1501 catenin delta 2 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000269|ECO:0000322 experimental evidence used in manual assertion|imported manually asserted information used in automatic assertion PMID:20038906 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1298228 Foxq1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:7080 NKX2-1 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000322|ECO:0000220|ECO:0000501 imported manually asserted information used in automatic assertion|sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:96915 Maoa NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15272015 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104629 Penk NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11172058 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95819 Grin1 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:24244696 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88145 Bdnf NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:17023662|PMID:11579207|PMID:17023662|PMID:20130183 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88497 Crhbp NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:10500222|PMID:10500222 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:1918639 Chd6 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20111866 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:1813 dopamine receptor D2 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:95583 Fshr NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:14502087 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:785 calcium channel, voltage-dependent, beta 4 subunit NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21703932|PMID:21683658|PMID:11319492|PMID:19453714|PMID:21041102 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:6387 chemokine (C-X-C motif) ligand 12 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:105120 Dusp1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:20953200 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:108067 Nkx2-1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17182767 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:109583 Pten NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16675393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:2563 gamma-aminobutyric acid (GABA) A receptor, delta NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:21703932|PMID:21683658|PMID:11319492|PMID:19453714|PMID:21041102 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:894312 Crhr2 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:11756502 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1201784 Oit1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:20562862|MGI:5000289 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+NCBIGene:6347 CCL2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:8851 cyclin-dependent kinase 5, regulatory subunit 1 (p35) NCBITaxon:9606 Homo sapiens MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:10706614 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4535 ND1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17854255|PMID:1759138|PMID:9172914|PMID:9602186|PMID:22796196 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:24225 Bdnf NCBITaxon:10116 Rattus norvegicus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:24768643 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1351641 Naglu NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10588735 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1916977 Usp46 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:19465912 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:7098 toll-like receptor 3 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1100513 Lmx1b NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:18695238 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88256 Camk2a NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:18295356|PMID:20145109|PMID:1378648|PMID:16400147|PMID:24503275 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl inferred
+NCBIGene:1827 RCAN1 NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22511596 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1346542 Bace1 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence PMID:14664815 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2679448 Slitrk5 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20418887 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:109521 Htr2a NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:16873667|PMID:16873667 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:96721 L1cam NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:9580664 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3067 histidine decarboxylase NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:8425124|PMID:20063404|PMID:8173824|PMID:1564054|PMID:23418216 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:109483 Rnf103 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19753093|PMID:18958194|PMID:18958194 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:104735 Gt(ROSA)26Sor NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:18832146 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88495 Crem NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18562617 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:7048 transforming growth factor beta receptor II NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:15857188|PMID:22773173|PMID:17587321|PMID:21883167|PMID:8539655 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:7068 THRB NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:17938043|PMID:9491171|PMID:24058526|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:101929036 LOC101929036 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000501 sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:99926 mt-Atp8 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19037013 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1351345 Grm8 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16045496 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95809 Gria2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:16216087|PMID:16099814 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3107 HLA-C NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1342774 Ppargc1a NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:15760270 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3064 huntingtin NCBITaxon:9606 Homo sapiens MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23001568 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:5063 PAK3 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000269 sequencing assay evidence|experimental evidence used in manual assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1261791 Apba2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19420255 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1101358 Npepps NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:10407043 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1929864 Myg1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19818808 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1355296 Park2 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:17883413 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1861942 Gtf2ird1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:17680805 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:22802 CLCA4 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000246 imported manually asserted information used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:20171652|PMID:12796866|PMID:7866213|PMID:20495477|PMID:10361400 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1097716 Arx NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:19587282 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6928 HNF1 homeobox B NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:53335 BCL11A NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000246|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213|ECO:0000213 combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21326311|PMID:21326311|PMID:21099065|PMID:21326311|PMID:21326311|PMID:23406172|PMID:21326311|PMID:3375880|PMID:25372704|PMID:21326311|PMID:17938043|PMID:9491171|PMID:21326311|PMID:21326311|PMID:21326311|PMID:21326311|PMID:21326311|PMID:21326311|PMID:21326311|PMID:21425450|PMID:25042611|PMID:21326311|PMID:21326311|PMID:21326311|PMID:21326311|PMID:21326311|PMID:21326311|PMID:21326311 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:108471 Ntan1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10805755 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2442479 Elfn1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:24312227 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104615 Cnr1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:12405999|PMID:15078564|PMID:11823890|PMID:23785142 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1932872 Ctns NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12370309 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1202717 Psen1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:22336193|PMID:24278307 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:208 AKT2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:351 APP NCBITaxon:9606 Homo sapiens MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:19936202|PMID:18184372|PMID:12742740|PMID:16876915|PMID:16289866|PMID:15016076 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98475 Tacr1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:11172050 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104798 Tnf NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11063830 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:348 apolipoprotein E NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:12354323|PMID:20629912|PMID:6462129|PMID:1829081|PMID:12014236 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1919835 Lypd1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19246390 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1351610 Npas3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:16190882 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1927169 B4galt5 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3609573 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:95757 Slc2a3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18780771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1889505 B3gnt2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:2685783 Baiap3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23698091 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2137383 Csmd1 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:24244513 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:108418 Npy2r NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:12742262 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:2006 ELN NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:12730029|PMID:21211940|PMID:22048961|PMID:21328569|PMID:22371147 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:95821 Grin2b NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:19081379|PMID:23201971|PMID:19081379|PMID:23201971 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:22475625 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:27030 mutL homolog 3 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:15857188|PMID:22773173|PMID:17587321|PMID:21883167|PMID:8539655 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:4916 NTRK3 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000213|ECO:0000246 combinatorial evidence used in automatic assertion|computational combinatorial evidence used in automatic assertion PMID:7554686|PMID:23510063|PMID:22388998|PMID:20635362|PMID:9333269|PMID:12581195 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2671987 Shank2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:22699619|PMID:22699620|PMID:22699619 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2148922 Ehmt2 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:20005824 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:107588 Gjb6 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12911759 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5646427 Tmr10 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence MGI:4940633 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:102723788 LOC102723788 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:7559318|PMID:15289208|PMID:1845224|PMID:2209418|PMID:20639284 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:88498 Crhr1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:21885734|PMID:10448190|PMID:9655498|PMID:12973355|PMID:9620773|PMID:9620773 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104735 Gt(ROSA)26Sor NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:19679071|PMID:19679071|PMID:18518923 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:99557 Pde4b NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:26272049 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1099446 Synpo NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:12928494 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:98824 Trhr NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17666589 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95564 Fmr1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19016890 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:23621 BACE1 NCBITaxon:9606 Homo sapiens MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:25100603|PMID:25100603 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88258 Camk4 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:20209163 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97384 Ntrk2 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:19158294|PMID:19158294|PMID:18832146|PMID:10571233 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:102707 Efna2 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:25281279 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:97535 Pdyn NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:12843270 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2671045 tmgc30 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006 experimental evidence MGI:2448159 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88497 Crhbp NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10500222|PMID:10500222 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+NCBIGene:4041 LRP5 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:21525520|PMID:21847749|PMID:75706|PMID:16137956|PMID:12099988 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2442354 Csgalnact1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence MGI:5000289|PMID:20562862 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:88105 Atp1a1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3609573 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+NCBIGene:3845 Kirsten rat sarcoma viral oncogene homolog NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000323 computational combinatorial evidence used in automatic assertion|imported automatically asserted information used in automatic assertion PMID:15857188|PMID:17587321|PMID:21883167|PMID:22773173|PMID:8539655 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:4287 ATXN3 NCBITaxon:9606 Homo sapiens MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence|experimental evidence PMID:19666958|PMID:19699305|PMID:19666958|PMID:19666958 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:6348 CCL3 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000177|ECO:0000246 genomic context evidence|computational combinatorial evidence used in automatic assertion PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:114327 EFHC1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000322|ECO:0000220|ECO:0000246 imported manually asserted information used in automatic assertion|sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:21703932|PMID:21683658|PMID:11319492|PMID:19453714|PMID:21041102 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:2152453 Gsk3a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20357757 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:105089 Hsd17b4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:23777740|PMID:23777740 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:2158 F9 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:3817455|PMID:10734657|PMID:18700841|PMID:19187190|PMID:7875359 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1195256 Pla2g4a NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:18931664|PMID:18931664 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:1371 CPOX NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000501|ECO:0000322 sequencing assay evidence|evidence used in automatic assertion|imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:96916 Maob NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15272015 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1929258 Kcnip3 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19223600 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104510 Myo7a NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:63673 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1890563 Wasf1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:12578964 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:4163 MCC NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000213 computational combinatorial evidence used in automatic assertion|combinatorial evidence used in automatic assertion PMID:21099065|PMID:3375880|PMID:21326311|PMID:17938043|PMID:9491171|PMID:21425450 http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1861234 Wt NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:13834122 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1201414 Cer1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88498 Crhr1 NCBITaxon:10090 Mus musculus HP:0000739 Anxiety ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:11756502|PMID:11756502|PMID:22231481 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95824 Nr3c1 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:10471508 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:1234 CCR5 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1277959 Dlg4 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23268962 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3990 LIPC NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:98735 Th NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16723393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:104735 Gt(ROSA)26Sor NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21885734 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:54902 tetratricopeptide repeat domain 19 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000501 sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:97602 Prkcz NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:23283171 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95819 Grin1 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19915563 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3667 insulin receptor substrate 1 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:111 adenylate cyclase 5 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000501|ECO:0000322|ECO:0000220|ECO:0000501 evidence used in automatic assertion|imported manually asserted information used in automatic assertion|sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:729230 CCR2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:12098612|PMID:22276472|PMID:3167473|PMID:2751944|PMID:2801829 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:54499 transmembrane and coiled-coil domains 1 NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000322|ECO:0000501|ECO:0000220|ECO:0000501 imported manually asserted information used in automatic assertion|evidence used in automatic assertion|sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:3584508 Kcnh5 NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:5646421 Mbt3 NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence MGI:4940633 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5515454 M1073b NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:5573 PRKAR1A NCBITaxon:9606 Homo sapiens HP:0000739 Anxiety ECO:0000220|ECO:0000501 sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:5982 RFC2 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000322 computational combinatorial evidence used in automatic assertion|imported manually asserted information used in automatic assertion PMID:12730029|PMID:21211940|PMID:22048961|PMID:21328569|PMID:22371147 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:95583 Fshr NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:14502087 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:88470 Comt NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9707588 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2139535 Tprn NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000059|ECO:0000059|ECO:0000006 experimental phenotypic evidence|experimental phenotypic evidence|experimental evidence MGI:5576271 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/impc.ttl inferred
+NCBIGene:3172 HNF4A NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000246|ECO:0000220 computational combinatorial evidence used in automatic assertion|sequencing assay evidence PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:97597 Prkcg NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006 experimental evidence PMID:10979601 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:95575 Fosb NCBITaxon:10090 Mus musculus MP:0001364 decreased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:21679928|PMID:21679928 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+NCBIGene:3767 potassium channel, inwardly rectifying subfamily J, member 11 NCBITaxon:9606 Homo sapiens HP:0000740 Anxiety (with pheochromocytoma) ECO:0000220|ECO:0000246 sequencing assay evidence|computational combinatorial evidence used in automatic assertion PMID:9428966|PMID:22188726|PMID:12429356|PMID:22397240|PMID:2209327 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+MGI:1098271 Rgs2 NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11027316 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
diff -r 000000000000 -r 850bb90bd667 test-data/genes-for-diseases.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/genes-for-diseases.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,130 @@
+NCBIGene:37853 Mlp60A NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:39002 Prm NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:627 BDNF NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3630 insulin NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2944 GSTM1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17449559 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:33824 Gpdh NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens OMIM:260540 Parkinson-Dementia Syndrome ECO:0000220|ECO:0000322 sequencing assay evidence|imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4729 NDUFV2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1565 CYP2D6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:15174030|PMID:14991823 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3482 insulin like growth factor 2 receptor NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4842 nitric oxide synthase 1 (neuronal) NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:26383258 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5243 ATP binding cassette subfamily B member 1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20558393 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:15882845|PMID:19946270|PMID:25149416|PMID:22043175|PMID:16573651|PMID:12588799|PMID:22841634|PMID:24582596|PMID:15198987|PMID:17010972|PMID:23628791 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4129 MAOB NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:43497 Obp99b NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens Orphanet:240112 Progressive supranuclear palsy - progressive non fluent aphasia ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:31826 rdgA NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19915575|PMID:23628791|PMID:25149416|PMID:23017109|PMID:20205471|PMID:22043175|PMID:23472874|PMID:19915576|PMID:17388990 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2244 FGB NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23233872 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6315 ATXN8OS NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:260300 autosomal recessive early-onset Parkinson disease 15 ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:2670 glial fibrillary acidic protein NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:3569 interleukin 6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4128 MAOA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17449559 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2747 GLUD2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4803 nerve growth factor (beta polypeptide) NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:199 AIF1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:168601 autosomal dominant Parkinson disease 1 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4287 ATXN3 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:203228 chromosome 9 open reading frame 72 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:4566 TRNK NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:6531 solute carrier family 6 (neurotransmitter transporter), member 3 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16112329|PMID:19590691|PMID:16963468|PMID:9763484 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6311 ATXN2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:53564 retinin NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:26281 fibroblast growth factor 20 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2203 FBP1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens OMIM:613643 Parkinson Disease 5, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4217 mitogen-activated protein kinase kinase kinase 5 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21815648 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3077 HFE NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16824219 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens OMIM:605543 Parkinson Disease 4, Autosomal Dominant ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens OMIM:607060 autosomal dominant Parkinson disease 8 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4929 NR4A2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:7345 UCHL1 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:55532 SLC30A10 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3313 HSPA9 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16565515 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177|PMID:19915575 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:3643 INSR NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2950 glutathione S-transferase pi 1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17190945|PMID:23721876 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:27429 HTRA2 NCBITaxon:9606 Homo sapiens OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:23400 ATP13A2 NCBITaxon:9606 Homo sapiens OMIM:606693 Kufor-Rakeb syndrome ECO:0000033|ECO:0000220|ECO:0000322|ECO:0000220 traceable author statement|sequencing assay evidence|imported manually asserted information used in automatic assertion|sequencing assay evidence PMID:22768177|PMID:22022275|PMID:22847264 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1728 NQO1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17188257 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:126 ADH1C NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:55737 VPS35 retromer complex component NCBITaxon:9606 Homo sapiens OMIM:614203 Parkinson Disease 17 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23037695|PMID:20800516|PMID:17010972|PMID:25149416|PMID:20423725|PMID:22898350|PMID:22043175|PMID:23792957|PMID:15784737 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:26058 GRB10 interacting GYF protein 2 NCBITaxon:9606 Homo sapiens OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:38508 Cpr64Aa NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3162 HMOX1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20664293|PMID:12151787|PMID:22355530|PMID:17690948|PMID:25149416|PMID:12732244|PMID:21245015|PMID:25064009|PMID:11535288|PMID:18353766|PMID:22166454|PMID:20711177|PMID:17131421|PMID:12885775|PMID:18322262|PMID:21892157|PMID:22043175|PMID:22185909|PMID:15099020|PMID:14535945|PMID:19915575|PMID:18841091|PMID:19915576|PMID:22110584 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+MGI:1857323 Up NCBITaxon:10090 Mus musculus DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:43829 ATPsynbeta NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:32133 Hsc70-3 NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:23317 DNAJC13 NCBITaxon:9606 Homo sapiens OMIM:616361 Parkinson Disease 21 ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:55737 VPS35 retromer complex component NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6908 TATA-box binding protein NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6202 RPS8 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1621 dopamine beta-hydroxylase (dopamine beta-monooxygenase) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4729 NDUFV2 NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:27429 HTRA2 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:683 BST1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19915576 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3480 insulin like growth factor 1 receptor NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:5071 parkin RBR E3 ubiquitin protein ligase NCBITaxon:9606 Homo sapiens OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:100129518 LOC100129518 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:17188257|PMID:18353766|PMID:25279756 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6147 ribosomal protein L23a NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:627 BDNF NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4540 MT-ND5 NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4535 ND1 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:43690 chp NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:23317 DNAJC13 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:38418 kst NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4541 MT-ND6 NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:6531 solute carrier family 6 (neurotransmitter transporter), member 3 NCBITaxon:9606 Homo sapiens OMIM:613135 Parkinsonism-Dystonia, Infantile ECO:0000322|ECO:0000220 imported manually asserted information used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3481 IGF2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4576 TRNT NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:1815 dopamine receptor D4 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:39826 fax NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1571 CYP2E1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16510128 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+NCBIGene:9829 DnaJ heat shock protein family (Hsp40) member C6 NCBITaxon:9606 Homo sapiens OMIM:615528 Parkinson Disease 19, Juvenile-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:9627 synuclein alpha interacting protein NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:2629 GBA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20947659|PMID:25064009 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:7124 tumor necrosis factor NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:21318773 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:9045 RPL14 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:33721 Rtnl1 NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens Orphanet:240094 Progressive supranuclear palsy - pure akinesia with gait freezing ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:497258 BDNF-AS NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4099 MAG NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:8867 SYNJ1 NCBITaxon:9606 Homo sapiens OMIM:615530 Parkinson Disease 20, Early-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:6128 ribosomal protein L6 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4540 MT-ND5 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:1981 eukaryotic translation initiation factor 4 gamma, 1 NCBITaxon:9606 Homo sapiens OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:2629 GBA NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl inferred
+NCBIGene:8398 phospholipase A2 group VI NCBITaxon:9606 Homo sapiens OMIM:612953 Parkinson Disease 14, Autosomal Recessive ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:6571 solute carrier family 18 (vesicular monoamine transporter), member 2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16112329 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:23400 ATP13A2 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:25149416|PMID:23628791 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:25793 F-box protein 7 NCBITaxon:9606 Homo sapiens OMIM:260300 autosomal recessive early-onset Parkinson disease 15 ECO:0000322|ECO:0000033|ECO:0000220 imported manually asserted information used in automatic assertion|traceable author statement|sequencing assay evidence PMID:25029497 http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset ECO:0000033|ECO:0000220 traceable author statement|sequencing assay evidence PMID:24475098|PMID:21421046 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:3122 HLA-DRA NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2580 GAK NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:20711177 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 ECO:0000323 imported automatically asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:44643 Cnx99A NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:2941 GSTA4 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:16510128 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:4541 MT-ND6 NCBITaxon:9606 Homo sapiens Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:33883 Cpr NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:126 ADH1C NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4571 MT-TP NCBITaxon:9606 Homo sapiens OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl inferred
+NCBIGene:4137 microtubule associated protein tau NCBITaxon:9606 Homo sapiens Orphanet:240103 Progressive supranuclear palsy - corticobasal syndrome ECO:0000322 imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl inferred
+NCBIGene:6888 TALDO1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:23233872 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1906 endothelin 1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19276553 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:11315 parkinson protein 7 NCBITaxon:9606 Homo sapiens OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset ECO:0000220 sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:38990 Cpr66D NCBITaxon:7227 Drosophila melanogaster DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:18353766 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:1356 ceruloplasmin (ferroxidase) NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:19159062|PMID:25758665 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:54822 TRPM7 NCBITaxon:9606 Homo sapiens OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 ECO:0000220|ECO:0000323 sequencing assay evidence|imported automatically asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/kegg.ttl|http://data.monarchinitiative.org/ttl/ctd.ttl inferred
+NCBIGene:65018 PINK1 NCBITaxon:9606 Homo sapiens DOID:14330 Parkinson's disease ECO:0000033 traceable author statement PMID:22043175|PMID:17010972|PMID:25149416|PMID:21366594|PMID:24374061 http://data.monarchinitiative.org/ttl/ctd.ttl inferred
diff -r 000000000000 -r 850bb90bd667 test-data/genes-for-phenotype.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/genes-for-phenotype.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,10 @@
+NCBIGene:26058 GRB10 interacting GYF protein 2 NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000220|ECO:0000269 sequencing assay evidence|experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:5428 polymerase (DNA directed), gamma NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501|ECO:0000220 evidence used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:2643 GCH1 NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000220|ECO:0000304 sequencing assay evidence|traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:25793 F-box protein 7 NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000322|ECO:0000220|ECO:0000501 imported manually asserted information used in automatic assertion|sequencing assay evidence|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:23400 ATP13A2 NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000220|ECO:0000322|ECO:0000220|ECO:0000304 sequencing assay evidence|imported manually asserted information used in automatic assertion|sequencing assay evidence|traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:7054 TH NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000322|ECO:0000304|ECO:0000220 imported manually asserted information used in automatic assertion|traceable author statement used in manual assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:27429 HTRA2 NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000220|ECO:0000304 sequencing assay evidence|traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:120892 leucine-rich repeat kinase 2 NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501|ECO:0000220 evidence used in automatic assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/gwascatalog.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:6872 TATA-box binding protein associated factor 1 NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304|ECO:0000220 traceable author statement used in manual assertion|sequencing assay evidence http://data.monarchinitiative.org/ttl/omim.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+NCBIGene:6622 SNCA NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501|ECO:0000322 evidence used in automatic assertion|imported manually asserted information used in automatic assertion http://data.monarchinitiative.org/ttl/orphanet.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
diff -r 000000000000 -r 850bb90bd667 test-data/homologues-for-gene.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/homologues-for-gene.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,30 @@
+NCBIGene:607311 CAPN10 NCBITaxon:9615 Canis lupus familiaris RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:84290 CAPNS2 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+WormBase:WBGene00006606 tra-3 NCBITaxon:6239 Caenorhabditis elegans RO:HOM0000017 in orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:6650 calpain 15 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:11131 CAPN11 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:79747 ADGB NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+MGI:1344392 Capn10 NCBITaxon:10090 Mus musculus RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:63834 Capn10 NCBITaxon:10116 Rattus norvegicus RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:147968 calpain 12 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:23473 CAPN7 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:440854 CAPN14 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:10753 CAPN9 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:570311 capn10 NCBITaxon:7955 Danio rerio RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000031|ECO:0000080 protein BLAST evidence used in manual assertion|phylogenetic evidence ZFIN:ZDB-PUB-030905-1 http://data.monarchinitiative.org/ttl/panther.ttl|http://data.monarchinitiative.org/ttl/zfin.ttl direct
+NCBIGene:827 CAPN6 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:553115 PEF1 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:826 CAPNS1 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:100022544 CAPN10 NCBITaxon:13616 Monodelphis domestica RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:6717 SRI NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:10016 PDCD6 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:388743 CAPN8 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:25801 GCA NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:824 CAPN2 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:716360 CAPN10 NCBITaxon:9544 Macaca mulatta RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:841981 DEK1 NCBITaxon:3702 Arabidopsis thaliana RO:HOM0000017 in orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:789674 CAPN10 NCBITaxon:9913 Bos taurus RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:825 calpain 3 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:100379827 capn10 NCBITaxon:8364 Xenopus tropicalis RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:726 CAPN5 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:823 calpain 1, (mu/I) large subunit NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:92291 CAPN13 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
diff -r 000000000000 -r 850bb90bd667 test-data/homologues-for-genes-intersection.tsv
diff -r 000000000000 -r 850bb90bd667 test-data/homologues-for-genes-union.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/homologues-for-genes-union.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,58 @@
+NCBIGene:607311 CAPN10 NCBITaxon:9615 Canis lupus familiaris RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:84290 CAPNS2 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+ZFIN:ZDB-GENE-030131-5206 capns1b NCBITaxon:7955 Danio rerio RO:HOM0000017 in orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+WormBase:WBGene00006606 tra-3 NCBITaxon:6239 Caenorhabditis elegans RO:HOM0000017 in orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:6650 calpain 15 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:10753 CAPN9 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:388743 CAPN8 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+MGI:1916793 Capns2 NCBITaxon:10090 Mus musculus RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:11131 CAPN11 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:79747 ADGB NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+MGI:1344392 Capn10 NCBITaxon:10090 Mus musculus RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:6717 SRI NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:825 calpain 3 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:79747 ADGB NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:823 calpain 1, (mu/I) large subunit NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080|ECO:0000079 phylogenetic evidence|affinity chromatography evidence PMID:26186194 http://data.monarchinitiative.org/ttl/panther.ttl|http://data.monarchinitiative.org/ttl/biogrid.ttl direct
+NCBIGene:6650 calpain 15 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:63834 Capn10 NCBITaxon:10116 Rattus norvegicus RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+ZFIN:ZDB-GENE-030113-3 capns1a NCBITaxon:7955 Danio rerio RO:HOM0000017 in orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:147968 calpain 12 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:553115 PEF1 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:23473 CAPN7 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:147968 calpain 12 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:440854 CAPN14 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:548915 capns2 NCBITaxon:8364 Xenopus tropicalis RO:HOM0000017 in orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:10753 CAPN9 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:570311 capn10 NCBITaxon:7955 Danio rerio RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000031|ECO:0000080 protein BLAST evidence used in manual assertion|phylogenetic evidence ZFIN:ZDB-PUB-030905-1 http://data.monarchinitiative.org/ttl/panther.ttl|http://data.monarchinitiative.org/ttl/zfin.ttl direct
+NCBIGene:827 CAPN6 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:553115 PEF1 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:830295 AT5G04170 NCBITaxon:3702 Arabidopsis thaliana RO:HOM0000017 in orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:826 CAPNS1 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:100022544 CAPN10 NCBITaxon:13616 Monodelphis domestica RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+WormBase:WBGene00019770 M04F3.4 NCBITaxon:6239 Caenorhabditis elegans RO:HOM0000017 in orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:827 CAPN6 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:6717 SRI NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:25801 GCA NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:440854 CAPN14 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:10016 PDCD6 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:388743 CAPN8 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:826 CAPNS1 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080|ECO:0000079 phylogenetic evidence|affinity chromatography evidence PMID:26186194 http://data.monarchinitiative.org/ttl/panther.ttl|http://data.monarchinitiative.org/ttl/biogrid.ttl direct
+NCBIGene:25801 GCA NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:824 CAPN2 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:92291 CAPN13 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:716360 CAPN10 NCBITaxon:9544 Macaca mulatta RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:11131 CAPN11 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:841981 DEK1 NCBITaxon:3702 Arabidopsis thaliana RO:HOM0000017 in orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:820192 AT3G10300 NCBITaxon:3702 Arabidopsis thaliana RO:HOM0000017 in orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:726 CAPN5 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:23473 CAPN7 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:789674 CAPN10 NCBITaxon:9913 Bos taurus RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:825 calpain 3 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:100145791 capns1 NCBITaxon:8364 Xenopus tropicalis RO:HOM0000017 in orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:11132 CAPN10 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:100379827 capn10 NCBITaxon:8364 Xenopus tropicalis RO:HOM0000020 in 1 to 1 orthology relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:824 CAPN2 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:726 CAPN5 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:823 calpain 1, (mu/I) large subunit NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:92291 CAPN13 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
+NCBIGene:10016 PDCD6 NCBITaxon:9606 Homo sapiens RO:HOM0000011 in paralogy relationship with ECO:0000080 phylogenetic evidence http://data.monarchinitiative.org/ttl/panther.ttl direct
diff -r 000000000000 -r 850bb90bd667 test-data/phenotype.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/phenotype.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,1 @@
+HP:0002548
\ No newline at end of file
diff -r 000000000000 -r 850bb90bd667 test-data/phenotypes-for-disease.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/phenotypes-for-disease.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,283 @@
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002019 Constipation ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:12814332|PMID:21560061|PMID:23408927|PMID:22021174|PMID:19717168 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0100660 Dyskinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002015 Dysphagia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0001824 Weight loss ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000739 Anxiety ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002020 Gastroesophageal reflux ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0100315 Lewy bodies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000011 Neurogenic bladder ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22331071|PMID:12922929|PMID:12756142|PMID:1965204|PMID:16855424 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001824 Weight loss ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20028343|PMID:16773618|PMID:15595933|PMID:11241387|PMID:21192784 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000605 Supranuclear gaze palsy ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0000012 Urinary urgency ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0001621 Weak voice ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0100315 Lewy bodies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22204976|PMID:23803637|PMID:16093408|PMID:23803638|PMID:16720791 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001266 Choreoathetosis ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:2330103|PMID:1052297|PMID:6457534|PMID:16364674|PMID:9686783 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000711 Restlessness ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20683503|PMID:21560064|PMID:2350935|PMID:12390050|PMID:23047004 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0001268 Mental deterioration ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0000726 Dementia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0003881 Humeral sclerosis ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21309754|PMID:10675426|PMID:9113500|PMID:22023479|PMID:19479510 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002076 Migraine ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22037955|PMID:16870487|PMID:3431838|PMID:15090934|PMID:16341290 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100022 Abnormality of movement ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21696993|PMID:22245219|PMID:17516489|PMID:17013911|PMID:17013922 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0000658 Eyelid apraxia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0011968 Feeding difficulties ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000975 Hyperhidrosis ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22021174|PMID:7818245|PMID:20022689|PMID:14673882|PMID:15834763 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0000571 Hypometric saccades ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0002362 Shuffling gait ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000726 Dementia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:14558483|PMID:11041086|PMID:22043625|PMID:23803637|PMID:11949709 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:616361 Parkinson Disease 21 RO:0002200 has phenotype HP:0100315 Lewy bodies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002511 Alzheimer disease ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:9843162|PMID:7652084|PMID:19367511|PMID:17514358|PMID:1311375 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:616361 Parkinson Disease 21 RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002367 Visual hallucinations ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:16720791|PMID:7652084|PMID:20933338|PMID:16239760|PMID:17516497 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002019 Constipation ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0003470 Paralysis ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:15728291|PMID:12654954|PMID:22130148|PMID:21560060|PMID:6231489 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0002366 Abnormal lower motor neuron morphology ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:14558491|PMID:15767513|PMID:17048150|PMID:8158173|PMID:20055267 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002359 Frequent falls ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20411272|PMID:10191839|PMID:21764079|PMID:22776044|PMID:18608364 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002304 Akinesia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21840512|PMID:2515716|PMID:3730813|PMID:21560065|PMID:9549521 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501|ECO:0000501 evidence used in automatic assertion|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000716 Depression ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0001336 Myoclonus ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0001347 Hyperreflexia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0011960 Substantia nigra gliosis ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0000726 Dementia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0011999 Paranoia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0003394 Muscle cramps ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0003236 Elevated serum creatine phosphokinase ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0007311 Short stepped shuffling gait ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100754 Mania ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:3167408|PMID:15291663|PMID:20205149|PMID:12034798|PMID:12465087 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002304 Akinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002307 Drooling ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:11340798|PMID:2130649|PMID:11340797|PMID:17892967|PMID:22021174 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0000605 Supranuclear gaze palsy ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:616361 Parkinson Disease 21 RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0001257 Spasticity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002062 Morphological abnormality of the pyramidal tract ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0100660 Dyskinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0007024 Pseudobulbar paralysis ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:3828155|PMID:8648326|PMID:3366147|PMID:8780066|PMID:12201229 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0002493 Upper motor neuron dysfunction ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002356 Writer's cramp ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17131231|PMID:3504239|PMID:19232169|PMID:2296384|PMID:9074398 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0003006 Neuroblastoma ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20026175|PMID:8341291|PMID:10737593|PMID:12787066|PMID:18411255 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000298 Mask-like facies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002018 Nausea ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17516484|PMID:21843110|PMID:19768728|PMID:2515717|PMID:6180142 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000716 Depression ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001347 Hyperreflexia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001336 Myoclonus ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:18686651|PMID:1965204|PMID:2067442|PMID:12465085|PMID:2350935 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0000718 Aggressive behavior ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001249 Intellectual disability ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17548778|PMID:21257332|PMID:8665730|PMID:1618013|PMID:12836419 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0001347 Hyperreflexia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001000 Abnormality of skin pigmentation ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:6499297|PMID:7715783|PMID:7771778|PMID:10737635|PMID:8731382 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0001263 Global developmental delay ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0003487 Babinski sign ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0002061 Lower limb spasticity ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002529 Neuronal loss in central nervous system ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:23380027|PMID:17516497|PMID:18715146|PMID:22899187|PMID:17931705 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000738 Hallucinations ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001257 Spasticity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0001347 Hyperreflexia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000012 Urinary urgency ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001268 Mental deterioration ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0002362 Shuffling gait ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0008936 Muscular hypotonia of the trunk ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002019 Constipation ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0001250 Seizures ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:616361 Parkinson Disease 21 RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0001278 Orthostatic hypotension ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000751 Personality changes ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002331 Headache (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20464588|PMID:1807237|PMID:326325|PMID:11195537|PMID:17370756 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000643 Blepharospasm ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002360 Sleep disturbance ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0011960 Substantia nigra gliosis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002362 Shuffling gait ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0001249 Intellectual disability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000725 Psychotic episodes ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0000726 Dementia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000012 Urinary urgency ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0000738 Hallucinations ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002174 Postural tremor ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:19067999|PMID:20055267|PMID:18456512|PMID:19242649|PMID:17048150 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0000751 Personality changes ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0001288 Gait disturbance ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001337 Tremor ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:14558490|PMID:22976499|PMID:23047004|PMID:11949716|PMID:17516492 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0001939 Abnormality of metabolism/homeostasis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002194 Delayed gross motor development ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0001347 Hyperreflexia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000726 Dementia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100753 Schizophrenia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:10447302|PMID:19396395|PMID:8789910|PMID:17027767|PMID:9171838 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002353 EEG abnormality ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:1714807|PMID:16483454|PMID:2605826|PMID:1753458|PMID:7489659 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0002751 Kyphoscoliosis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000020 Urinary incontinence ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:12814332|PMID:15895303|PMID:19135266|PMID:22331072|PMID:20429324 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000733 Stereotypic behavior ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21072531|PMID:563012|PMID:16934409|PMID:3670611|PMID:6138131 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100660 Dyskinesia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17013916|PMID:7146724|PMID:22043624|PMID:17516484|PMID:21729402 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0011951 Aspiration pneumonia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21098406|PMID:12970031|PMID:12404752|PMID:20518603|PMID:20869620 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0004409 Hyposmia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17508142|PMID:22035024|PMID:18322371|PMID:21560061|PMID:21387694 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002167 Neurological speech impairment ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:19864662|PMID:8162135|PMID:15767513|PMID:22772465|PMID:22706836 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0002283 Global brain atrophy ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002072 Chorea ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0000298 Mask-like facies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002615 Hypotension ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:7296422|PMID:6441537|PMID:1300258|PMID:6180142|PMID:1300256 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20055267|PMID:12948464|PMID:3747258|PMID:17048150|PMID:22130147 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0002071 Abnormality of extrapyramidal motor function ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0000605 Supranuclear gaze palsy ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000726 Dementia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002360 Sleep disturbance ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100315 Lewy bodies ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22043625|PMID:22245218|PMID:20055267|PMID:16093408|PMID:17516497 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000738 Hallucinations ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0000726 Dementia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001278 Orthostatic hypotension ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21560061|PMID:16906622|PMID:12654979|PMID:12814332|PMID:5386267 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000725 Psychotic episodes ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0000514 Slow saccadic eye movements ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20055267|PMID:9426865|PMID:19176228|PMID:19858460|PMID:17048150 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0001337 Tremor ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000718 Aggressive behavior ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0002312 Clumsiness ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0004409 Hyposmia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000458 Anosmia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100543 Cognitive impairment ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:18178571|PMID:17516457|PMID:9387801|PMID:18682443|PMID:20832408 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000738 Hallucinations ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22043626|PMID:19507125|PMID:12814332|PMID:19680598|PMID:17548778 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0001336 Myoclonus ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0004409 Hyposmia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0003487 Babinski sign ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0006892 Frontotemporal cerebral atrophy ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002936 Distal sensory impairment ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000473 Torticollis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0001762 Talipes equinovarus ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002425 Anarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0002304 Akinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0001257 Spasticity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000726 Dementia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000298 Mask-like facies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0001324 Muscle weakness ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0002459 Dysautonomia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0002062 Morphological abnormality of the pyramidal tract ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002529 Neuronal loss in central nervous system ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100595 Camptocormia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17027115|PMID:19864661|PMID:21389682|PMID:12671947|PMID:23994926 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0001250 Seizures ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002493 Upper motor neuron dysfunction ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002459 Dysautonomia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0002493 Upper motor neuron dysfunction ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0001268 Mental deterioration ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000722 Obsessive-compulsive behavior ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20205149|PMID:15639176|PMID:21764406|PMID:22604202|PMID:23318227 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002180 Neurodegeneration ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20865164|PMID:23040108|PMID:23019375|PMID:17255333|PMID:16720791 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000739 Anxiety ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:616361 Parkinson Disease 21 RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002015 Dysphagia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002385 Paraparesis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0012407 Scissor gait ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001324 Muscle weakness ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:8682529|PMID:17931671|PMID:15372591|PMID:18313370|PMID:7659761 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002017 Nausea and vomiting ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:15495119|PMID:7195483|PMID:10091630|PMID:6481422|PMID:9756144 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0000597 Ophthalmoparesis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002174 Postural tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000017 Nocturia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:11741097|PMID:8369103|PMID:19404716|PMID:20205139|PMID:21264941 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0011960 Substantia nigra gliosis ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0007354 Amyotrophic lateral sclerosis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002072 Chorea ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:1656540|PMID:1557069|PMID:21729402|PMID:9387799|PMID:39737 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0010524 Agnosia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:2932922|PMID:12796834|PMID:15782604|PMID:9686278|PMID:3263977 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000709 Psychosis ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21630354|PMID:12814332|PMID:17013906|PMID:10727476|PMID:22245219 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002451 Limb dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22402215|PMID:11949716|PMID:9513304|PMID:20055267|PMID:17048150 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:2515718|PMID:6231489|PMID:22976499|PMID:2579626|PMID:7715793 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000514 Slow saccadic eye movements ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0001283 Bulbar palsy ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0001288 Gait disturbance ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000751 Personality changes ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21560061|PMID:16908734|PMID:21845593|PMID:9426865|PMID:18346925 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:616361 Parkinson Disease 21 RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002321 Vertigo ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:19479494|PMID:21843110|PMID:19768728|PMID:2515717|PMID:12814332 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000746 Delusions ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:12814332|PMID:16239760|PMID:7652084|PMID:19507125|PMID:20538500 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000822 Hypertension ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:18166127|PMID:20032288|PMID:11041086|PMID:17761552|PMID:17514358 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0100315 Lewy bodies ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000012 Urinary urgency ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:3942028|PMID:14521485|PMID:18327532|PMID:19908315|PMID:11570707 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
diff -r 000000000000 -r 850bb90bd667 test-data/phenotypes-for-diseases-intersection.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/phenotypes-for-diseases-intersection.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,22 @@
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002015 Dysphagia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0001621 Weak voice ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0100315 Lewy bodies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0007311 Short stepped shuffling gait ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000716 Depression ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000012 Urinary urgency ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002019 Constipation ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000751 Personality changes ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002360 Sleep disturbance ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0011960 Substantia nigra gliosis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000726 Dementia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000738 Hallucinations ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000298 Mask-like facies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002529 Neuronal loss in central nervous system ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002459 Dysautonomia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
diff -r 000000000000 -r 850bb90bd667 test-data/phenotypes-for-diseases-union.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/phenotypes-for-diseases-union.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,283 @@
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002019 Constipation ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:12814332|PMID:21560061|PMID:23408927|PMID:22021174|PMID:19717168 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0100660 Dyskinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002015 Dysphagia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0001824 Weight loss ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000739 Anxiety ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002020 Gastroesophageal reflux ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0100315 Lewy bodies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000011 Neurogenic bladder ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22331071|PMID:12922929|PMID:12756142|PMID:1965204|PMID:16855424 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001824 Weight loss ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20028343|PMID:16773618|PMID:15595933|PMID:11241387|PMID:21192784 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000605 Supranuclear gaze palsy ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0000012 Urinary urgency ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0001621 Weak voice ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0100315 Lewy bodies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22204976|PMID:23803637|PMID:16093408|PMID:23803638|PMID:16720791 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001266 Choreoathetosis ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:2330103|PMID:1052297|PMID:6457534|PMID:16364674|PMID:9686783 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000711 Restlessness ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20683503|PMID:21560064|PMID:2350935|PMID:12390050|PMID:23047004 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0001268 Mental deterioration ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0000726 Dementia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0003881 Humeral sclerosis ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21309754|PMID:10675426|PMID:9113500|PMID:22023479|PMID:19479510 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002076 Migraine ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22037955|PMID:16870487|PMID:3431838|PMID:15090934|PMID:16341290 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100022 Abnormality of movement ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21696993|PMID:22245219|PMID:17516489|PMID:17013911|PMID:17013922 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0000658 Eyelid apraxia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0011968 Feeding difficulties ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000975 Hyperhidrosis ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22021174|PMID:7818245|PMID:20022689|PMID:14673882|PMID:15834763 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0000571 Hypometric saccades ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0002362 Shuffling gait ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000726 Dementia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:14558483|PMID:11041086|PMID:22043625|PMID:23803637|PMID:11949709 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:616361 Parkinson Disease 21 RO:0002200 has phenotype HP:0100315 Lewy bodies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002511 Alzheimer disease ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:9843162|PMID:7652084|PMID:19367511|PMID:17514358|PMID:1311375 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:616361 Parkinson Disease 21 RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002367 Visual hallucinations ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:16720791|PMID:7652084|PMID:20933338|PMID:16239760|PMID:17516497 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002019 Constipation ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0003470 Paralysis ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:15728291|PMID:12654954|PMID:22130148|PMID:21560060|PMID:6231489 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0002366 Abnormal lower motor neuron morphology ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:14558491|PMID:15767513|PMID:17048150|PMID:8158173|PMID:20055267 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002359 Frequent falls ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20411272|PMID:10191839|PMID:21764079|PMID:22776044|PMID:18608364 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002304 Akinesia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21840512|PMID:2515716|PMID:3730813|PMID:21560065|PMID:9549521 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501|ECO:0000501 evidence used in automatic assertion|evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000716 Depression ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0001336 Myoclonus ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0001347 Hyperreflexia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0011960 Substantia nigra gliosis ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0000726 Dementia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0011999 Paranoia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0003394 Muscle cramps ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0003236 Elevated serum creatine phosphokinase ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0007311 Short stepped shuffling gait ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100754 Mania ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:3167408|PMID:15291663|PMID:20205149|PMID:12034798|PMID:12465087 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002304 Akinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002307 Drooling ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:11340798|PMID:2130649|PMID:11340797|PMID:17892967|PMID:22021174 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0000605 Supranuclear gaze palsy ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:616361 Parkinson Disease 21 RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0001257 Spasticity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002062 Morphological abnormality of the pyramidal tract ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0100660 Dyskinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0007024 Pseudobulbar paralysis ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:3828155|PMID:8648326|PMID:3366147|PMID:8780066|PMID:12201229 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0002493 Upper motor neuron dysfunction ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002356 Writer's cramp ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17131231|PMID:3504239|PMID:19232169|PMID:2296384|PMID:9074398 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0003006 Neuroblastoma ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20026175|PMID:8341291|PMID:10737593|PMID:12787066|PMID:18411255 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000298 Mask-like facies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002018 Nausea ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17516484|PMID:21843110|PMID:19768728|PMID:2515717|PMID:6180142 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000716 Depression ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001347 Hyperreflexia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001336 Myoclonus ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:18686651|PMID:1965204|PMID:2067442|PMID:12465085|PMID:2350935 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0000718 Aggressive behavior ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001249 Intellectual disability ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17548778|PMID:21257332|PMID:8665730|PMID:1618013|PMID:12836419 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0001347 Hyperreflexia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001000 Abnormality of skin pigmentation ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:6499297|PMID:7715783|PMID:7771778|PMID:10737635|PMID:8731382 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0001263 Global developmental delay ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0003487 Babinski sign ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0002061 Lower limb spasticity ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002529 Neuronal loss in central nervous system ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:23380027|PMID:17516497|PMID:18715146|PMID:22899187|PMID:17931705 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000738 Hallucinations ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001257 Spasticity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0001347 Hyperreflexia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000012 Urinary urgency ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001268 Mental deterioration ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0002362 Shuffling gait ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0008936 Muscular hypotonia of the trunk ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002019 Constipation ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0001250 Seizures ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:616361 Parkinson Disease 21 RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0001278 Orthostatic hypotension ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000751 Personality changes ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002331 Headache (with pheochromocytoma) ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20464588|PMID:1807237|PMID:326325|PMID:11195537|PMID:17370756 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000643 Blepharospasm ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002360 Sleep disturbance ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0011960 Substantia nigra gliosis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002362 Shuffling gait ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0001249 Intellectual disability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000725 Psychotic episodes ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0000726 Dementia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000012 Urinary urgency ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0000738 Hallucinations ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002174 Postural tremor ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:19067999|PMID:20055267|PMID:18456512|PMID:19242649|PMID:17048150 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0000751 Personality changes ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0001288 Gait disturbance ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001337 Tremor ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:14558490|PMID:22976499|PMID:23047004|PMID:11949716|PMID:17516492 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0001939 Abnormality of metabolism/homeostasis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002194 Delayed gross motor development ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0001347 Hyperreflexia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000726 Dementia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100753 Schizophrenia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:10447302|PMID:19396395|PMID:8789910|PMID:17027767|PMID:9171838 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002353 EEG abnormality ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:1714807|PMID:16483454|PMID:2605826|PMID:1753458|PMID:7489659 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0002751 Kyphoscoliosis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000020 Urinary incontinence ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:12814332|PMID:15895303|PMID:19135266|PMID:22331072|PMID:20429324 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000733 Stereotypic behavior ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21072531|PMID:563012|PMID:16934409|PMID:3670611|PMID:6138131 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100660 Dyskinesia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17013916|PMID:7146724|PMID:22043624|PMID:17516484|PMID:21729402 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0011951 Aspiration pneumonia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21098406|PMID:12970031|PMID:12404752|PMID:20518603|PMID:20869620 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0004409 Hyposmia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17508142|PMID:22035024|PMID:18322371|PMID:21560061|PMID:21387694 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002167 Neurological speech impairment ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:19864662|PMID:8162135|PMID:15767513|PMID:22772465|PMID:22706836 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0002283 Global brain atrophy ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002072 Chorea ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0000298 Mask-like facies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002615 Hypotension ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:7296422|PMID:6441537|PMID:1300258|PMID:6180142|PMID:1300256 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20055267|PMID:12948464|PMID:3747258|PMID:17048150|PMID:22130147 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0002071 Abnormality of extrapyramidal motor function ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0000605 Supranuclear gaze palsy ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000726 Dementia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002360 Sleep disturbance ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100315 Lewy bodies ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22043625|PMID:22245218|PMID:20055267|PMID:16093408|PMID:17516497 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000738 Hallucinations ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0000726 Dementia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001278 Orthostatic hypotension ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21560061|PMID:16906622|PMID:12654979|PMID:12814332|PMID:5386267 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000725 Psychotic episodes ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0000514 Slow saccadic eye movements ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20055267|PMID:9426865|PMID:19176228|PMID:19858460|PMID:17048150 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0001337 Tremor ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000718 Aggressive behavior ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0002312 Clumsiness ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0004409 Hyposmia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000458 Anosmia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100543 Cognitive impairment ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:18178571|PMID:17516457|PMID:9387801|PMID:18682443|PMID:20832408 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000738 Hallucinations ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22043626|PMID:19507125|PMID:12814332|PMID:19680598|PMID:17548778 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0001260 Dysarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0001336 Myoclonus ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607060 autosomal dominant Parkinson disease 8 RO:0002200 has phenotype HP:0004409 Hyposmia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0003487 Babinski sign ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0006892 Frontotemporal cerebral atrophy ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002936 Distal sensory impairment ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000473 Torticollis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0001762 Talipes equinovarus ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002425 Anarthria ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0002304 Akinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0001257 Spasticity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000726 Dementia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0000298 Mask-like facies ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0001324 Muscle weakness ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0002459 Dysautonomia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0002062 Morphological abnormality of the pyramidal tract ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002529 Neuronal loss in central nervous system ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0100595 Camptocormia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:17027115|PMID:19864661|PMID:21389682|PMID:12671947|PMID:23994926 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0001250 Seizures ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002493 Upper motor neuron dysfunction ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002459 Dysautonomia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0002493 Upper motor neuron dysfunction ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0001268 Mental deterioration ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000722 Obsessive-compulsive behavior ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20205149|PMID:15639176|PMID:21764406|PMID:22604202|PMID:23318227 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002180 Neurodegeneration ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:20865164|PMID:23040108|PMID:23019375|PMID:17255333|PMID:16720791 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0000739 Anxiety ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168600 Parkinson Disease, Late-Onset RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:616361 Parkinson Disease 21 RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168601 autosomal dominant Parkinson disease 1 RO:0002200 has phenotype HP:0002015 Dysphagia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002385 Paraparesis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260300 autosomal recessive early-onset Parkinson disease 15 RO:0002200 has phenotype HP:0012407 Scissor gait ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001324 Muscle weakness ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:8682529|PMID:17931671|PMID:15372591|PMID:18313370|PMID:7659761 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002017 Nausea and vomiting ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:15495119|PMID:7195483|PMID:10091630|PMID:6481422|PMID:9756144 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:260540 Parkinson-Dementia Syndrome RO:0002200 has phenotype HP:0000597 Ophthalmoparesis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:612953 Parkinson Disease 14, Autosomal Recessive RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset RO:0002200 has phenotype HP:0002174 Postural tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615530 Parkinson Disease 20, Early-Onset RO:0002200 has phenotype HP:0001337 Tremor ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000017 Nocturia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:11741097|PMID:8369103|PMID:19404716|PMID:20205139|PMID:21264941 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0011960 Substantia nigra gliosis ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0007354 Amyotrophic lateral sclerosis ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002072 Chorea ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:1656540|PMID:1557069|PMID:21729402|PMID:9387799|PMID:39737 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0010524 Agnosia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:2932922|PMID:12796834|PMID:15782604|PMID:9686278|PMID:3263977 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000709 Psychosis ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21630354|PMID:12814332|PMID:17013906|PMID:10727476|PMID:22245219 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:613135 Parkinsonism-Dystonia, Infantile RO:0002200 has phenotype HP:0002451 Limb dystonia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:22402215|PMID:11949716|PMID:9513304|PMID:20055267|PMID:17048150 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:168100 Paralysis Agitans, Juvenile, of Hunt RO:0002200 has phenotype HP:0002063 Rigidity ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0001332 Dystonia ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:2515718|PMID:6231489|PMID:22976499|PMID:2579626|PMID:7715793 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002067 Bradykinesia ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:606693 Kufor-Rakeb syndrome RO:0002200 has phenotype HP:0000514 Slow saccadic eye movements ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:614203 Parkinson Disease 17 RO:0002200 has phenotype HP:0001300 Parkinsonism ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:615528 Parkinson Disease 19, Juvenile-Onset RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:105500 Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1 RO:0002200 has phenotype HP:0001283 Bulbar palsy ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile RO:0002200 has phenotype HP:0001288 Gait disturbance ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000751 Personality changes ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:21560061|PMID:16908734|PMID:21845593|PMID:9426865|PMID:18346925 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:616361 Parkinson Disease 21 RO:0002200 has phenotype HP:0002172 Postural instability ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0002321 Vertigo ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:19479494|PMID:21843110|PMID:19768728|PMID:2515717|PMID:12814332 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to RO:0002200 has phenotype HP:0002322 Resting tremor ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000746 Delusions ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:12814332|PMID:16239760|PMID:7652084|PMID:19507125|PMID:20538500 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000822 Hypertension ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:18166127|PMID:20032288|PMID:11041086|PMID:17761552|PMID:17514358 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+OMIM:605543 Parkinson Disease 4, Autosomal Dominant RO:0002200 has phenotype HP:0100315 Lewy bodies ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/hpoa.ttl direct
+DOID:14330 Parkinson's disease RO:0002200 has phenotype HP:0000012 Urinary urgency ECO:0000246 computational combinatorial evidence used in automatic assertion PMID:3942028|PMID:14521485|PMID:18327532|PMID:19908315|PMID:11570707 http://data.monarchinitiative.org/ttl/hpoa.ttl direct
diff -r 000000000000 -r 850bb90bd667 test-data/phenotypes-for-variant.json
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/phenotypes-for-variant.json Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,1 @@
+{"phenopacket":{"phenotype_profile":[{"entity":"ClinVarVariant:217207","phenotype":{"types":[{"id":"HP:0010535","label":"Sleep apnea"}]}},{"entity":"FlyBase:FBal0213223","phenotype":{"types":[{"id":"FBcv:0000352","label":"partially lethal - majority die"}]}},{"entity":"ClinVarVariant:11487","phenotype":{"types":[{"id":"HP:0001829","label":"Foot polydactyly"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022219-WBRNAi00094335","phenotype":{"types":[{"id":"WBPhenotype:0000508","label":"nonsense mRNA accumulation"}]}},{"entity":"FlyBase:FBal0204990","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"FlyBase:FBal0094697","phenotype":{"types":[{"id":"FBcv:0000395","label":"locomotor rhythm defective"}]}},{"entity":"ClinVarVariant:126392","phenotype":{"types":[{"id":"HP:0001433","label":"Hepatosplenomegaly"}]}},{"entity":"ClinVarVariant:167486","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:161253","phenotype":{"types":[{"id":"HP:0011096","label":"Peripheral demyelination"}]}},{"entity":"ClinVarVariant:24488","phenotype":{"types":[{"id":"HP:0000517","label":"Abnormality of the lens"}]}},{"entity":"ClinVarVariant:10038","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"ClinVarVariant:120292","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:91630","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:188714","phenotype":{"types":[{"id":"HP:0002015","label":"Dysphagia"}]}},{"entity":"ClinVarVariant:65078","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:13919","phenotype":{"types":[{"id":"HP:0002527","label":"Falls"}]}},{"entity":"ClinVarVariant:166796","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"ClinVarVariant:53300","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:49671","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:6383","phenotype":{"types":[{"id":"HP:0002758","label":"Osteoarthritis"}]}},{"entity":"ClinVarVariant:12869","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:3241","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"MGI:1856875","phenotype":{"types":[{"id":"MP:0000377","label":"abnormal hair follicle morphology"}]}},{"entity":"ClinVarVariant:24448","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"NCBIGene:553991","phenotype":{"types":[{"id":"HP:0003805","label":"Rimmed vacuoles"}]}},{"entity":"ClinVarVariant:35614","phenotype":{"types":[{"id":"HP:0001518","label":"Small for gestational age"}]}},{"entity":"ClinVarVariant:24856","phenotype":{"types":[{"id":"HP:0001636","label":"Tetralogy of Fallot"}]}},{"entity":"ClinVarVariant:135244","phenotype":{"types":[{"id":"HP:0100819","label":"Intestinal fistula"}]}},{"entity":"MGI:3702572","phenotype":{"types":[{"id":"MP:0001327","label":"decreased retinal photoreceptor cell number"}]}},{"entity":"ClinVarVariant:204248","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002981-WBRNAi00083915","phenotype":{"types":[{"id":"WBPhenotype:0001171","label":"shortened life span"}]}},{"entity":"ClinVarVariant:10490","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007201-WBRNAi00062819","phenotype":{"types":[{"id":"WBPhenotype:0000691","label":"gonad development variant"}]}},{"entity":"MGI:2182460","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"dbSNP:rs2202157","phenotype":{"types":[{"id":"HP:0009733","label":"Glioma"}]}},{"entity":"ClinVarVariant:49410","phenotype":{"types":[{"id":"HP:0100764","label":"Lymphangioma"}]}},{"entity":"ClinVarVariant:101209","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"MGI:2684419","phenotype":{"types":[{"id":"MP:0008190","label":"decreased transitional stage B cell number"}]}},{"entity":"MGI:2671609","phenotype":{"types":[{"id":"MP:0011279","label":"decreased ear pigmentation"}]}},{"entity":"ClinVarVariant:215956","phenotype":{"types":[{"id":"HP:0000324","label":"Facial asymmetry"}]}},{"entity":"ClinVarVariant:49985","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"dbSNP:rs1819084","phenotype":{"types":[{"id":"HP:0002721","label":"Immunodeficiency"}]}},{"entity":"ClinVarVariant:42347","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"ClinVarVariant:10746","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"dbSNP:rs10720414","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"ClinVarVariant:100901","phenotype":{"types":[{"id":"HP:0008420","label":"Punctate vertebral calcifications"}]}},{"entity":"ClinVarVariant:40523","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:3975","phenotype":{"types":[{"id":"HP:0000121","label":"Nephrocalcinosis"}]}},{"entity":"ClinVarVariant:191776","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:3243","phenotype":{"types":[{"id":"HP:0001274","label":"Agenesis of corpus callosum"}]}},{"entity":"ClinVarVariant:49691","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:53303","phenotype":{"types":[{"id":"HP:0100732","label":"Pancreatic fibrosis"}]}},{"entity":"MGI:3046930","phenotype":{"types":[{"id":"MP:0008828","label":"abnormal lymph node cell ratio"}]}},{"entity":"ClinVarVariant:10947","phenotype":{"types":[{"id":"HP:0002007","label":"Frontal bossing"}]}},{"entity":"ClinVarVariant:208036","phenotype":{"types":[{"id":"HP:0000280","label":"Coarse facial features"}]}},{"entity":"ClinVarVariant:216123","phenotype":{"types":[{"id":"HP:0001350","label":"Slurred speech"}]}},{"entity":"ClinVarVariant:10634","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"ClinVarVariant:13684","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:53955","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:42536","phenotype":{"types":[{"id":"HP:0001297","label":"Stroke"}]}},{"entity":"dbSNP:rs109157116","phenotype":{"types":[{"id":"AQTLTrait:1067","label":"Length of productive life"}]}},{"entity":"ClinVarVariant:143822","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:208497","phenotype":{"types":[{"id":"HP:0002179","label":"Opisthotonus"}]}},{"entity":"ClinVarVariant:42838","phenotype":{"types":[{"id":"HP:0003712","label":"Skeletal muscle hypertrophy"}]}},{"entity":"ClinVarVariant:53165","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"MGI:2159365","phenotype":{"types":[{"id":"HP:0005528","label":"Bone marrow hypocellularity"}]}},{"entity":"ClinVarVariant:65088","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:40601","phenotype":{"types":[{"id":"HP:0008443","label":"Spinal deformities"}]}},{"entity":"ClinVarVariant:10128","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"MGI:2178049","phenotype":{"types":[{"id":"MP:0001405","label":"impaired coordination"}]}},{"entity":"FlyBase:FBal0294203","phenotype":{"types":[{"id":"FBbt:00001920PHENOTYPE","label":"embryonic/larval brain phenotype"}]}},{"entity":"ClinVarVariant:5007","phenotype":{"types":[{"id":"HP:0001182","label":"Tapered finger"}]}},{"entity":"ClinVarVariant:363","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:184551","phenotype":{"types":[{"id":"HP:0002216","label":"Premature graying of hair"}]}},{"entity":"MGI:3834217","phenotype":{"types":[{"id":"MP:0002841","label":"impaired skeletal muscle contractility"}]}},{"entity":"ClinVarVariant:45379","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:158297","phenotype":{"types":[{"id":"HP:0010761","label":"Broad columella"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004470-WBRNAi00085516","phenotype":{"types":[{"id":"WBPhenotype:0001954","label":"diplotene absent during oogenesis"}]}},{"entity":"ClinVarVariant:7309","phenotype":{"types":[{"id":"HP:0000954","label":"Single transverse palmar crease"}]}},{"entity":"ClinVarVariant:11580","phenotype":{"types":[{"id":"HP:0002007","label":"Frontal bossing"}]}},{"entity":"ClinVarVariant:7057","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:10283","phenotype":{"types":[{"id":"HP:0100710","label":"Impulsivity"}]}},{"entity":"ClinVarVariant:8492","phenotype":{"types":[{"id":"HP:0001332","label":"Dystonia"}]}},{"entity":"MGI:3841488","phenotype":{"types":[{"id":"HP:0004324","label":"Increased body weight"}]}},{"entity":"ClinVarVariant:189720","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"MGI:5140883","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"MGI:2182765","phenotype":{"types":[{"id":"MP:0001257","label":"increased body length"}]}},{"entity":"ClinVarVariant:39667","phenotype":{"types":[{"id":"HP:0001067","label":"Neurofibromas"}]}},{"entity":"ClinVarVariant:690","phenotype":{"types":[{"id":"HP:0010471","label":"Oligosacchariduria"}]}},{"entity":"ClinVarVariant:38952","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:215911","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:143120","phenotype":{"types":[{"id":"HP:0001653","label":"Mitral regurgitation"}]}},{"entity":"ClinVarVariant:159945","phenotype":{"types":[{"id":"HP:0002465","label":"Poor speech"}]}},{"entity":"ClinVarVariant:45183","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"ClinVarVariant:66101","phenotype":{"types":[{"id":"HP:0004469","label":"Chronic bronchitis"}]}},{"entity":"ClinVarVariant:127491","phenotype":{"types":[{"id":"HP:0000377","label":"Abnormality of the pinna"}]}},{"entity":"ClinVarVariant:208829","phenotype":{"types":[{"id":"HP:0009601","label":"Aplasia/Hypoplasia of the thumb"}]}},{"entity":"ClinVarVariant:24772","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:36051","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:158343","phenotype":{"types":[{"id":"HP:0000742","label":"Self-mutilation"}]}},{"entity":"dbSNP:rs10172646","phenotype":{"types":[{"id":"HP:0001931","label":"Hypochromic anemia"}]}},{"entity":"ClinVarVariant:56735","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:162049","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:12595","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"ClinVarVariant:13342","phenotype":{"types":[{"id":"HP:0002861","label":"Melanoma"}]}},{"entity":"ClinVarVariant:184560","phenotype":{"types":[{"id":"HP:0009734","label":"Optic glioma"}]}},{"entity":"ClinVarVariant:5985","phenotype":{"types":[{"id":"HP:0003119","label":"Abnormality of lipid metabolism"}]}},{"entity":"ClinVarVariant:92534","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:17178","phenotype":{"types":[{"id":"HP:0006149","label":"Increased laxity of fingers"}]}},{"entity":"FlyBase:FBal0137361","phenotype":{"types":[{"id":"FBbt:00005634PHENOTYPE","label":"Drosophila embryonic Malpighian tubule phenotype"}]}},{"entity":"ClinVarVariant:99942","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"MGI:1891594","phenotype":{"types":[{"id":"HP:0008222","label":"Female infertility"}]}},{"entity":"ClinVarVariant:53953","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:64885","phenotype":{"types":[{"id":"HP:0003881","label":"Humeral sclerosis"}]}},{"entity":"ClinVarVariant:180352","phenotype":{"types":[{"id":"HP:0002835","label":"Aspiration"}]}},{"entity":"ClinVarVariant:2023","phenotype":{"types":[{"id":"HP:0000830","label":"Anterior hypopituitarism"}]}},{"entity":"ClinVarVariant:94505","phenotype":{"types":[{"id":"HP:0002948","label":"Vertebral fusion"}]}},{"entity":"ClinVarVariant:12048","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"AQTL:20712","phenotype":{"types":[{"id":"AQTLTrait:1114","label":"Body length"}]}},{"entity":"MGI:1932294","phenotype":{"types":[{"id":"HP:0012819","label":"Myocarditis"}]}},{"entity":"ClinVarVariant:12493","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"ClinVarVariant:12589","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:24660","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:48937","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:13960","phenotype":{"types":[{"id":"HP:0002208","label":"Coarse hair"}]}},{"entity":"ClinVarVariant:21062","phenotype":{"types":[{"id":"HP:0000660","label":"Lipemia retinalis"}]}},{"entity":"ClinVarVariant:158712","phenotype":{"types":[{"id":"HP:0009237","label":"Short 5th finger"}]}},{"entity":"ClinVarVariant:11931","phenotype":{"types":[{"id":"HP:0001376","label":"Limitation of joint mobility"}]}},{"entity":"ClinVarVariant:204128","phenotype":{"types":[{"id":"HP:0100758","label":"Gangrene"}]}},{"entity":"ClinVarVariant:35880","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:155757","phenotype":{"types":[{"id":"HP:0001539","label":"Omphalocele"}]}},{"entity":"FlyBase:FBal0298766","phenotype":{"types":[{"id":"FBbt:00007250PHENOTYPE","label":"Drosophila inter-ommatidial cell phenotype"}]}},{"entity":"ClinVarVariant:189801","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"ClinVarVariant:167312","phenotype":{"types":[{"id":"HP:0002027","label":"Abdominal pain"}]}},{"entity":"ClinVarVariant:159955","phenotype":{"types":[{"id":"HP:0002465","label":"Poor speech"}]}},{"entity":"ClinVarVariant:127747","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:373","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"MGI:1861456","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"FlyBase:FBal0150123","phenotype":{"types":[{"id":"FBbt:00004970PHENOTYPE","label":"cuticle phenotype"}]}},{"entity":"FlyBase:FBal0183487","phenotype":{"types":[{"id":"FBcv:0000430","label":"cell polarity defective"}]}},{"entity":"ClinVarVariant:11218","phenotype":{"types":[{"id":"HP:0001685","label":"Myocardial fibrosis"}]}},{"entity":"MGI:5311370","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"ClinVarVariant:10497","phenotype":{"types":[{"id":"HP:0011855","label":"Pharyngeal edema"}]}},{"entity":"ClinVarVariant:53319","phenotype":{"types":[{"id":"HP:0100027","label":"Recurrent pancreatitis"}]}},{"entity":"ClinVarVariant:49838","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:68576","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:10572","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"MGI:4454555","phenotype":{"types":[{"id":"MP:0001745","label":"increased circulating corticosterone level"}]}},{"entity":"ClinVarVariant:97593","phenotype":{"types":[{"id":"HP:0005214","label":"Intestinal obstruction"}]}},{"entity":"ClinVarVariant:161981","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"ClinVarVariant:40512","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:188788","phenotype":{"types":[{"id":"HP:0000649","label":"Abnormality of visual evoked potentials"}]}},{"entity":"ClinVarVariant:10174","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:38289","phenotype":{"types":[{"id":"HP:0002196","label":"Myelopathy"}]}},{"entity":"ClinVarVariant:2334","phenotype":{"types":[{"id":"HP:0001315","label":"Reduced tendon reflexes"}]}},{"entity":"ClinVarVariant:64739","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:177995","phenotype":{"types":[{"id":"HP:0001279","label":"Syncope"}]}},{"entity":"ClinVarVariant:53999","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:181735","phenotype":{"types":[{"id":"HP:0008572","label":"External ear malformation"}]}},{"entity":"ClinVarVariant:11712","phenotype":{"types":[{"id":"HP:0001388","label":"Joint laxity"}]}},{"entity":"ClinVarVariant:38324","phenotype":{"types":[{"id":"HP:0000046","label":"Scrotal hypoplasia"}]}},{"entity":"ClinVarVariant:11077","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:7151","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:9141","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:188928","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:9064","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017241-WBRNAi00096241","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-001103-2-ZDB-MRPHLNO-041110-4-ZDB-MRPHLNO-050322-1","phenotype":{"types":[{"id":"ZP:0000064","label":"abnormal(ly) decreased size ceratohyal cartilage"}]}},{"entity":"ClinVarVariant:40680","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:210726","phenotype":{"types":[{"id":"HP:0001231","label":"Abnormality of the fingernails"}]}},{"entity":"MGI:3584018","phenotype":{"types":[{"id":"HP:0100827","label":"Lymphocytosis"}]}},{"entity":"NCBIGene:100526741","phenotype":{"types":[{"id":"HP:0002823","label":"Abnormality of the femur"}]}},{"entity":"ClinVarVariant:42317","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"ClinVarVariant:12786","phenotype":{"types":[{"id":"HP:0001028","label":"Hemangioma"}]}},{"entity":"MGI:4450934","phenotype":{"types":[{"id":"MP:0002188","label":"small heart"}]}},{"entity":"ClinVarVariant:43594","phenotype":{"types":[{"id":"HP:0002488","label":"Acute leukemia"}]}},{"entity":"ClinVarVariant:211626","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"FlyBase:FBal0206465","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:159239","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:156048","phenotype":{"types":[{"id":"HP:0002270","label":"Abnormality of the autonomic nervous system"}]}},{"entity":"ClinVarVariant:24478","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:40565","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"dbSNP:rs41625970","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:1461","phenotype":{"types":[{"id":"HP:0007359","label":"Focal seizures"}]}},{"entity":"ClinVarVariant:9581","phenotype":{"types":[{"id":"HP:0002401","label":"Stroke-like episodes"}]}},{"entity":"ClinVarVariant:21170","phenotype":{"types":[{"id":"HP:0001511","label":"Intrauterine growth retardation"}]}},{"entity":"ClinVarVariant:189700","phenotype":{"types":[{"id":"HP:0000478","label":"Abnormality of the eye"}]}},{"entity":"ClinVarVariant:14067","phenotype":{"types":[{"id":"HP:0001712","label":"Left ventricular hypertrophy"}]}},{"entity":"ClinVarVariant:49844","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:36848","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:16901","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:100938","phenotype":{"types":[{"id":"HP:0007018","label":"Attention deficit hyperactivity disorder"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000817-WBRNAi00073502","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:46499","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"dbSNP:rs41597892","phenotype":{"types":[{"id":"AQTLTrait:1101","label":"Foot angle"}]}},{"entity":"ClinVarVariant:167132","phenotype":{"types":[{"id":"HP:0000225","label":"Gingival bleeding"}]}},{"entity":"FlyBase:FBal0151927","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"AQTL:33210","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001210-WBRNAi00090496","phenotype":{"types":[{"id":"WBPhenotype:0001645","label":"protein degradation variant"}]}},{"entity":"ClinVarVariant:94504","phenotype":{"types":[{"id":"HP:0008443","label":"Spinal deformities"}]}},{"entity":"ClinVarVariant:4950","phenotype":{"types":[{"id":"HP:0005855","label":"Multiple prenatal fractures"}]}},{"entity":"ClinVarVariant:3331","phenotype":{"types":[{"id":"HP:0001575","label":"Mood changes"}]}},{"entity":"ClinVarVariant:210258","phenotype":{"types":[{"id":"HP:0007360","label":"Aplasia/Hypoplasia of the cerebellum"}]}},{"entity":"ClinVarVariant:101203","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"AQTL:1008","phenotype":{"types":[{"id":"AQTLTrait:3088","label":"Shoulder muscle weight"}]}},{"entity":"ClinVarVariant:24227","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:6011","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:43690","phenotype":{"types":[{"id":"HP:0000268","label":"Dolichocephaly"}]}},{"entity":"FlyBase:FBal0237989","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"MGI:2180062","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:25201","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:142320","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:36061","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:180362","phenotype":{"types":[{"id":"HP:0002835","label":"Aspiration"}]}},{"entity":"MGI:5301308","phenotype":{"types":[{"id":"MP:0004810","label":"decreased hematopoietic stem cell number"}]}},{"entity":"ClinVarVariant:156447","phenotype":{"types":[{"id":"HP:0000138","label":"Ovarian cyst"}]}},{"entity":"ClinVarVariant:10905","phenotype":{"types":[{"id":"HP:0002716","label":"Lymphadenopathy"}]}},{"entity":"ClinVarVariant:94260","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:3282","phenotype":{"types":[{"id":"HP:0009588","label":"Vestibular Schwannoma"}]}},{"entity":"ClinVarVariant:65095","phenotype":{"types":[{"id":"HP:0009727","label":"Achromatic retinal patches"}]}},{"entity":"ClinVarVariant:30186","phenotype":{"types":[{"id":"HP:0100021","label":"Cerebral palsy"}]}},{"entity":"ClinVarVariant:607","phenotype":{"types":[{"id":"HP:0100753","label":"Schizophrenia"}]}},{"entity":"ZFIN:ZDB-ALT-070117-12","phenotype":{"types":[{"id":"ZP:0008988","label":"abnormal(ly) disrupted regulation of hydrogen peroxide metabolic process"}]}},{"entity":"FlyBase:FBal0318121","phenotype":{"types":[{"id":"FBbt:00000015PHENOTYPE","label":"Drosophila thorax phenotype"}]}},{"entity":"ClinVarVariant:9153","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"ClinVarVariant:2240","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"WormBase:WBVar00087821","phenotype":{"types":[{"id":"WBPhenotype:0001384","label":"fertility reduced"}]}},{"entity":"ClinVarVariant:466","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:53630","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:136044","phenotype":{"types":[{"id":"HP:0001587","label":"Primary ovarian failure"}]}},{"entity":"ClinVarVariant:137633","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"MGI:2386179","phenotype":{"types":[{"id":"HP:0012533","label":"Allodynia"}]}},{"entity":"ClinVarVariant:217059","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:137950","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"ClinVarVariant:18045","phenotype":{"types":[{"id":"HP:0004850","label":"Recurrent deep vein thrombosis"}]}},{"entity":"ClinVarVariant:4407","phenotype":{"types":[{"id":"HP:0002200","label":"Pseudobulbar signs"}]}},{"entity":"FlyBase:FBal0045026","phenotype":{"types":[{"id":"FBbt:00004223PHENOTYPE","label":"Drosophila photoreceptor cell R6 phenotype"}]}},{"entity":"ClinVarVariant:36948","phenotype":{"types":[{"id":"HP:0002206","label":"Pulmonary fibrosis"}]}},{"entity":"ClinVarVariant:161343","phenotype":{"types":[{"id":"HP:0001038","label":"Warfarin-induced skin necrosis"}]}},{"entity":"dbSNP:rs6538140","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"MGI:5449877","phenotype":{"types":[{"id":"HP:0002069","label":"Generalized tonic-clonic seizures"}]}},{"entity":"MGI:3845814","phenotype":{"types":[{"id":"MP:0010957","label":"abnormal aerobic respiration"}]}},{"entity":"ClinVarVariant:11369","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:2821","phenotype":{"types":[{"id":"HP:0007074","label":"Thick corpus callosum"}]}},{"entity":"ClinVarVariant:101186","phenotype":{"types":[{"id":"HP:0000387","label":"Absent earlobe"}]}},{"entity":"ClinVarVariant:6059","phenotype":{"types":[{"id":"HP:0003693","label":"Distal amyotrophy"}]}},{"entity":"dbSNP:rs81270306","phenotype":{"types":[{"id":"AQTLTrait:1023","label":"Hindquarter muscle weight"}]}},{"entity":"ClinVarVariant:18277","phenotype":{"types":[{"id":"HP:0002381","label":"Aphasia"}]}},{"entity":"ClinVarVariant:159096","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:41068","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:4394","phenotype":{"types":[{"id":"HP:0000540","label":"Hypermetropia"}]}},{"entity":"ClinVarVariant:12761","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:39786","phenotype":{"types":[{"id":"HP:0000414","label":"Bulbous nose"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004891-WBRNAi00083804","phenotype":{"types":[{"id":"WBPhenotype:0000812","label":"germ cell development variant"}]}},{"entity":"ClinVarVariant:55942","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:35849","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:156130","phenotype":{"types":[{"id":"HP:0010808","label":"Protruding tongue"}]}},{"entity":"FlyBase:FBal0154542","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:35845","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:65098","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:4943","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:41155","phenotype":{"types":[{"id":"HP:0000286","label":"Epicanthus"}]}},{"entity":"ClinVarVariant:10269","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:211718","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"ClinVarVariant:25026","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"ClinVarVariant:37090","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"WormBase:WBVar00248883","phenotype":{"types":[{"id":"WBPhenotype:0001744","label":"cell adhesion variant"}]}},{"entity":"FlyBase:FBal0042573","phenotype":{"types":[{"id":"FBbt:00005744PHENOTYPE","label":"Drosophila embryonic dorsal epidermis phenotype"}]}},{"entity":"ClinVarVariant:64739","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:35723","phenotype":{"types":[{"id":"HP:0000934","label":"Chondrocalcinosis"}]}},{"entity":"ClinVarVariant:94179","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"ClinVarVariant:18333","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"MGI:2156985","phenotype":{"types":[{"id":"MP:0002177","label":"abnormal outer ear morphology"}]}},{"entity":"ClinVarVariant:6717","phenotype":{"types":[{"id":"HP:0001900","label":"Increased hemoglobin"}]}},{"entity":"ClinVarVariant:139529","phenotype":{"types":[{"id":"HP:0000179","label":"Thick lower lip vermilion"}]}},{"entity":"ClinVarVariant:190378","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-040426-2906-ZDB-MRPHLNO-100915-2-ZDB-MRPHLNO-100915-3","phenotype":{"types":[{"id":"ZP:0000962","label":"abnormal(ly) disrupted axonal fasciculation"}]}},{"entity":"ClinVarVariant:189083","phenotype":{"types":[{"id":"HP:0000510","label":"Rod-cone dystrophy"}]}},{"entity":"ClinVarVariant:21255","phenotype":{"types":[{"id":"HP:0002797","label":"Osteolysis"}]}},{"entity":"ClinVarVariant:7215","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:49540","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:209029","phenotype":{"types":[{"id":"HP:0000777","label":"Abnormality of the thymus"}]}},{"entity":"ClinVarVariant:10313","phenotype":{"types":[{"id":"HP:0100309","label":"Subdural hemorrhage"}]}},{"entity":"MGI:5462249","phenotype":{"types":[{"id":"MP:0004532","label":"abnormal inner hair cell stereociliary bundle morphology"}]}},{"entity":"ClinVarVariant:158349","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:12844","phenotype":{"types":[{"id":"HP:0008341","label":"Distal renal tubular acidosis"}]}},{"entity":"FlyBase:FBal0052396","phenotype":{"types":[{"id":"FBbt:00000155PHENOTYPE","label":"Drosophila embryonic head phenotype"}]}},{"entity":"MGI:2180685","phenotype":{"types":[{"id":"MP:0005093","label":"decreased B cell proliferation"}]}},{"entity":"ClinVarVariant:188728","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:10748","phenotype":{"types":[{"id":"HP:0000763","label":"Sensory neuropathy"}]}},{"entity":"ClinVarVariant:24841","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:7750","phenotype":{"types":[{"id":"HP:0012062","label":"Bone cyst"}]}},{"entity":"MGI:4431694","phenotype":{"types":[{"id":"HP:0009887","label":"Abnormality of hair pigmentation"}]}},{"entity":"MGI:3037859","phenotype":{"types":[{"id":"MP:0001394","label":"circling"}]}},{"entity":"ClinVarVariant:40553","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:6927","phenotype":{"types":[{"id":"HP:0004416","label":"Precocious atherosclerosis"}]}},{"entity":"ClinVarVariant:13361","phenotype":{"types":[{"id":"HP:0009830","label":"Peripheral neuropathy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011480-WBRNAi00071460","phenotype":{"types":[{"id":"WBPhenotype:0001425","label":"receptor mediated endocytosis defective"}]}},{"entity":"NCBIGene:100187724","phenotype":{"types":[{"id":"HP:0001161","label":"Hand polydactyly"}]}},{"entity":"ClinVarVariant:189254","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:210769","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:159222","phenotype":{"types":[{"id":"HP:0011951","label":"Aspiration pneumonia"}]}},{"entity":"ClinVarVariant:198999","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"ClinVarVariant:126817","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:189603","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:136156","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:6551","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"ClinVarVariant:128454","phenotype":{"types":[{"id":"HP:0100579","label":"Mucosal telangiectasiae"}]}},{"entity":"ClinVarVariant:93346","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"WormBase:WBVar00090199","phenotype":{"types":[{"id":"WBPhenotype:0001221","label":"nose touch defective"}]}},{"entity":"ClinVarVariant:2141","phenotype":{"types":[{"id":"HP:0009829","label":"Phocomelia"}]}},{"entity":"ClinVarVariant:940","phenotype":{"types":[{"id":"HP:0003053","label":"Epiphyseal deformities of tubular bones"}]}},{"entity":"ClinVarVariant:53705","phenotype":{"types":[{"id":"HP:0004936","label":"Venous thrombosis"}]}},{"entity":"ClinVarVariant:204184","phenotype":{"types":[{"id":"HP:0012622","label":"Chronic kidney disease"}]}},{"entity":"ClinVarVariant:5396","phenotype":{"types":[{"id":"HP:0001655","label":"Patent foramen ovale"}]}},{"entity":"MGI:1934013","phenotype":{"types":[{"id":"MP:0008810","label":"increased circulating iron level"}]}},{"entity":"ClinVarVariant:50009","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:211665","phenotype":{"types":[{"id":"HP:0000413","label":"Atresia of the external auditory canal"}]}},{"entity":"ClinVarVariant:24243","phenotype":{"types":[{"id":"HP:0012622","label":"Chronic kidney disease"}]}},{"entity":"MGI:4836722","phenotype":{"types":[{"id":"HP:0040216","label":"Hypoinsulinemia"}]}},{"entity":"ClinVarVariant:159226","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:143858","phenotype":{"types":[{"id":"HP:0002376","label":"Developmental regression"}]}},{"entity":"FlyBase:FBal0285352","phenotype":{"types":[{"id":"FBbt:00004580PHENOTYPE","label":"Drosophila mesothoracic tergum phenotype"}]}},{"entity":"ClinVarVariant:101219","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:25321","phenotype":{"types":[{"id":"HP:0100626","label":"Chronic hepatic failure"}]}},{"entity":"MGI:3775093","phenotype":{"types":[{"id":"MP:0002052","label":"decreased tumor incidence"}]}},{"entity":"ClinVarVariant:143832","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000201-WBRNAi00088651","phenotype":{"types":[{"id":"WBPhenotype:0002057","label":"Bacillus thuringiensis toxin hypersensitive"}]}},{"entity":"MGI:5295482","phenotype":{"types":[{"id":"HP:0012447","label":"Abnormal myelination"}]}},{"entity":"ClinVarVariant:40243","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:188151","phenotype":{"types":[{"id":"HP:0002894","label":"Neoplasm of the pancreas"}]}},{"entity":"ClinVarVariant:16332","phenotype":{"types":[{"id":"HP:0003811","label":"Neonatal death"}]}},{"entity":"ClinVarVariant:24723","phenotype":{"types":[{"id":"HP:0030034","label":"Diffuse glomerular basement membrane lamellation"}]}},{"entity":"ClinVarVariant:82781","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"MGI:2384028","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:48104","phenotype":{"types":[{"id":"HP:0100272","label":"Branchial sinus"}]}},{"entity":"ClinVarVariant:2666","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:5849","phenotype":{"types":[{"id":"HP:0000684","label":"Delayed eruption of teeth"}]}},{"entity":"MGI:3047571","phenotype":{"types":[{"id":"MP:0008178","label":"decreased germinal center B cell number"}]}},{"entity":"ClinVarVariant:141579","phenotype":{"types":[{"id":"HP:0002216","label":"Premature graying of hair"}]}},{"entity":"ClinVarVariant:6395","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"AQTL:2263","phenotype":{"types":[{"id":"AQTLTrait:2048","label":"Drumstick weight"}]}},{"entity":"ClinVarVariant:158183","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"MGI:3575756","phenotype":{"types":[{"id":"MP:0001874","label":"acanthosis"}]}},{"entity":"ClinVarVariant:53638","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"FlyBase:FBal0297233","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:17494","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:5033","phenotype":{"types":[{"id":"HP:0003477","label":"Peripheral axonal neuropathy"}]}},{"entity":"ClinVarVariant:17370","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:190796","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"MGI:4839367","phenotype":{"types":[{"id":"MP:0009716","label":"abnormal subcommissural organ morphology"}]}},{"entity":"ClinVarVariant:135746","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:188246","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:53626","phenotype":{"types":[{"id":"HP:0006510","label":"Chronic obstructive pulmonary disease"}]}},{"entity":"ClinVarVariant:215765","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:88863","phenotype":{"types":[{"id":"HP:0011108","label":"Recurrent sinusitis"}]}},{"entity":"ClinVarVariant:67956","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:159118","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:21249","phenotype":{"types":[{"id":"HP:0006487","label":"Bowing of the long bones"}]}},{"entity":"ClinVarVariant:207996","phenotype":{"types":[{"id":"HP:0002749","label":"Osteomalacia"}]}},{"entity":"ClinVarVariant:215985","phenotype":{"types":[{"id":"HP:0000612","label":"Iris coloboma"}]}},{"entity":"ClinVarVariant:36081","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:97710","phenotype":{"types":[{"id":"HP:0001596","label":"Alopecia"}]}},{"entity":"FlyBase:FBal0242010","phenotype":{"types":[{"id":"FBbt:00006029PHENOTYPE","label":"Drosophila wing pouch phenotype"}]}},{"entity":"ClinVarVariant:41196","phenotype":{"types":[{"id":"HP:0010535","label":"Sleep apnea"}]}},{"entity":"ClinVarVariant:10136","phenotype":{"types":[{"id":"HP:0005261","label":"Joint hemorrhage"}]}},{"entity":"ClinVarVariant:189623","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"FlyBase:FBal0159231","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:4280","phenotype":{"types":[{"id":"HP:0001053","label":"Hypopigmented skin patches"}]}},{"entity":"ClinVarVariant:65546","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"MGI:1857691","phenotype":{"types":[{"id":"MP:0013216","label":"absent ectoderm"}]}},{"entity":"ClinVarVariant:53178","phenotype":{"types":[{"id":"HP:0100582","label":"Nasal polyposis"}]}},{"entity":"ClinVarVariant:24385","phenotype":{"types":[{"id":"HP:0000093","label":"Proteinuria"}]}},{"entity":"ClinVarVariant:92893","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:21402","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:188745","phenotype":{"types":[{"id":"HP:0001982","label":"Sea-blue histiocytosis"}]}},{"entity":"MGI:1857129","phenotype":{"types":[{"id":"MP:0005386","label":"behavior/neurological phenotype"}]}},{"entity":"ClinVarVariant:159897","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"dbSNP:rs41581462","phenotype":{"types":[{"id":"AQTLTrait:1173","label":"Rear leg set"}]}},{"entity":"ClinVarVariant:41182","phenotype":{"types":[{"id":"HP:0003162","label":"Fasting hypoglycemia"}]}},{"entity":"ClinVarVariant:36062","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:21585","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:210013","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:7112","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:101239","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:41354","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:42353","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"ZFIN:ZDB-ALT-040721-22","phenotype":{"types":[{"id":"ZP:0000100","label":"abnormal(ly) morphology brain"}]}},{"entity":"ClinVarVariant:24444","phenotype":{"types":[{"id":"HP:0007763","label":"Retinal telangiectasia"}]}},{"entity":"MGI:2179136","phenotype":{"types":[{"id":"MP:0006011","label":"abnormal endolymphatic duct morphology"}]}},{"entity":"ClinVarVariant:167477","phenotype":{"types":[{"id":"HP:0005576","label":"Tubulointerstitial fibrosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003834-WBRNAi00040618","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:127355","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"MGI:3609477","phenotype":{"types":[{"id":"MP:0002169","label":"no abnormal phenotype detected"}]}},{"entity":"ClinVarVariant:215464","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"ClinVarVariant:36082","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"MGI:2158467","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:8880","phenotype":{"types":[{"id":"HP:0000863","label":"Central diabetes insipidus"}]}},{"entity":"ClinVarVariant:202211","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ClinVarVariant:48035","phenotype":{"types":[{"id":"HP:0003198","label":"Myopathy"}]}},{"entity":"MGI:1857117","phenotype":{"types":[{"id":"HP:0000961","label":"Cyanosis"}]}},{"entity":"ClinVarVariant:7175","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"MGI:1861705","phenotype":{"types":[{"id":"MP:0000133","label":"abnormal long bone metaphysis morphology"}]}},{"entity":"ZFIN:ZDB-ALT-150203-1","phenotype":{"types":[{"id":"ZP:0012596","label":"abnormal(ly) has extra parts of type compact layer of ventricle basal cortex towards compact layer of ventricle cardiac myofibril"}]}},{"entity":"ClinVarVariant:38975","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:38321","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"FlyBase:FBal0124001","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:143788","phenotype":{"types":[{"id":"HP:0000478","label":"Abnormality of the eye"}]}},{"entity":"ClinVarVariant:36072","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:100921","phenotype":{"types":[{"id":"HP:0007359","label":"Focal seizures"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00016117-WBRNAi00027443","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:211667","phenotype":{"types":[{"id":"HP:0000776","label":"Congenital diaphragmatic hernia"}]}},{"entity":"MGI:2388372","phenotype":{"types":[{"id":"HP:0001941","label":"Acidosis"}]}},{"entity":"ClinVarVariant:190366","phenotype":{"types":[{"id":"HP:0002493","label":"Upper motor neuron dysfunction"}]}},{"entity":"ClinVarVariant:5710","phenotype":{"types":[{"id":"HP:0002179","label":"Opisthotonus"}]}},{"entity":"ClinVarVariant:8470","phenotype":{"types":[{"id":"HP:0003551","label":"Difficulty climbing stairs"}]}},{"entity":"MGI:3775302","phenotype":{"types":[{"id":"HP:0010783","label":"Erythema"}]}},{"entity":"OMIM:242840","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"MGI:4949192","phenotype":{"types":[{"id":"HP:0002242","label":"Abnormality of the intestine"}]}},{"entity":"AQTL:32413","phenotype":{"types":[{"id":"AQTLTrait:1004","label":"Somatic cell count"}]}},{"entity":"ClinVarVariant:66013","phenotype":{"types":[{"id":"HP:0001075","label":"Atrophic scars"}]}},{"entity":"ClinVarVariant:24976","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:31196","phenotype":{"types":[{"id":"HP:0003805","label":"Rimmed vacuoles"}]}},{"entity":"ClinVarVariant:52358","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:162065","phenotype":{"types":[{"id":"HP:0009773","label":"Symphalangism affecting the phalanges of the hand"}]}},{"entity":"ClinVarVariant:197868","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"MGI:2663662","phenotype":{"types":[{"id":"HP:0001875","label":"Neutropenia"}]}},{"entity":"ClinVarVariant:3296","phenotype":{"types":[{"id":"HP:0008069","label":"Neoplasm of the skin"}]}},{"entity":"MGI:4999600","phenotype":{"types":[{"id":"MP:0004971","label":"dermal hyperplasia"}]}},{"entity":"FlyBase:FBal0207033","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:11510","phenotype":{"types":[{"id":"HP:0002938","label":"Lumbar hyperlordosis"}]}},{"entity":"ClinVarVariant:29737","phenotype":{"types":[{"id":"HP:0000602","label":"Ophthalmoplegia"}]}},{"entity":"ClinVarVariant:53902","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00015538-WBRNAi00027160","phenotype":{"types":[{"id":"WBPhenotype:0000697","label":"protruding vulva"}]}},{"entity":"ClinVarVariant:53905","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:36042","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:14889","phenotype":{"types":[{"id":"HP:0008740","label":"Longitudinal vaginal septum"}]}},{"entity":"ClinVarVariant:65064","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"FlyBase:FBal0210388","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:41141","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:10589","phenotype":{"types":[{"id":"HP:0100845","label":"Anaphylactic shock"}]}},{"entity":"ClinVarVariant:12464","phenotype":{"types":[{"id":"HP:0002058","label":"Myopathic facies"}]}},{"entity":"ClinVarVariant:8240","phenotype":{"types":[{"id":"HP:0008947","label":"Infantile muscular hypotonia"}]}},{"entity":"ClinVarVariant:135755","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:210036","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"FlyBase:FBal0240836","phenotype":{"types":[{"id":"FBbt:00004930PHENOTYPE","label":"hub cell phenotype"}]}},{"entity":"dbSNP:rs826221","phenotype":{"types":[{"id":"HP:0002063","label":"Rigidity"}]}},{"entity":"ClinVarVariant:181725","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:161997","phenotype":{"types":[{"id":"HP:0006280","label":"Chronic pancreatitis"}]}},{"entity":"ClinVarVariant:25370","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"dbSNP:rs4869931","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"ClinVarVariant:35870","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"MGI:3530536","phenotype":{"types":[{"id":"MP:0001475","label":"reduced long term depression"}]}},{"entity":"ClinVarVariant:5343","phenotype":{"types":[{"id":"HP:0000968","label":"Ectodermal dysplasia"}]}},{"entity":"MGI:4459078","phenotype":{"types":[{"id":"MP:0010053","label":"decreased grip strength"}]}},{"entity":"ClinVarVariant:132900","phenotype":{"types":[{"id":"HP:0000726","label":"Dementia"}]}},{"entity":"ClinVarVariant:35666","phenotype":{"types":[{"id":"HP:0100530","label":"Abnormality of calcium-phosphate metabolism"}]}},{"entity":"ClinVarVariant:159961","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ClinVarVariant:159118","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"MGI:2154514","phenotype":{"types":[{"id":"HP:0008516","label":"Abnormality of the vertebral spinous processes"}]}},{"entity":"ClinVarVariant:67814","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:840","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:127737","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:24696","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"ClinVarVariant:102431","phenotype":{"types":[{"id":"HP:0001800","label":"Hypoplastic toenails"}]}},{"entity":"MGI:1857257","phenotype":{"types":[{"id":"MP:0008214","label":"increased immature B cell number"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000066-WBRNAi00095708","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:36052","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:11520","phenotype":{"types":[{"id":"HP:0002938","label":"Lumbar hyperlordosis"}]}},{"entity":"ClinVarVariant:163758","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:127415","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:159007","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:9694","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"FlyBase:FBal0305269","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:5616","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:35865","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:43212","phenotype":{"types":[{"id":"HP:0000360","label":"Tinnitus"}]}},{"entity":"ClinVarVariant:24528","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:96387","phenotype":{"types":[{"id":"HP:0100720","label":"Hypoplasia of the ear cartilage"}]}},{"entity":"AQTL:27380","phenotype":{"types":[{"id":"AQTLTrait:1485","label":"Mean corpuscular volume"}]}},{"entity":"ClinVarVariant:156068","phenotype":{"types":[{"id":"HP:0002270","label":"Abnormality of the autonomic nervous system"}]}},{"entity":"ClinVarVariant:210773","phenotype":{"types":[{"id":"HP:0010562","label":"Keloids"}]}},{"entity":"ClinVarVariant:188044","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"FlyBase:FBal0249096","phenotype":{"types":[{"id":"FBbt:00100216PHENOTYPE","label":"dopaminergic PPM1 neuron phenotype"}]}},{"entity":"ClinVarVariant:197559","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:36963","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"dbSNP:rs80879875","phenotype":{"types":[{"id":"AQTLTrait:456","label":"Hemoglobin"}]}},{"entity":"ClinVarVariant:7442","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"MGI:3053810","phenotype":{"types":[{"id":"MP:0002404","label":"increased intestinal adenoma incidence"}]}},{"entity":"ClinVarVariant:190185","phenotype":{"types":[{"id":"HP:0002282","label":"Heterotopia"}]}},{"entity":"ClinVarVariant:138714","phenotype":{"types":[{"id":"HP:0200134","label":"Epileptic encephalopathy"}]}},{"entity":"ClinVarVariant:184231","phenotype":{"types":[{"id":"HP:0001376","label":"Limitation of joint mobility"}]}},{"entity":"ClinVarVariant:2915","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:29732","phenotype":{"types":[{"id":"HP:0002126","label":"Polymicrogyria"}]}},{"entity":"ClinVarVariant:54023","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:143714","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ZFIN:ZDB-ALT-060519-4","phenotype":{"types":[{"id":"ZP:0000041","label":"abnormal(ly) quality pharyngeal arch 3-7 skeleton"}]}},{"entity":"ClinVarVariant:24765","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:2666","phenotype":{"types":[{"id":"HP:0012368","label":"Flat face"}]}},{"entity":"ClinVarVariant:184969","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"ClinVarVariant:7935","phenotype":{"types":[{"id":"HP:0000077","label":"Abnormality of the kidney"}]}},{"entity":"ZFIN:ZDB-ALT-090424-3","phenotype":{"types":[{"id":"ZP:0008370","label":"abnormal(ly) absent gall bladder"}]}},{"entity":"ClinVarVariant:180710","phenotype":{"types":[{"id":"HP:0002151","label":"Increased serum lactate"}]}},{"entity":"ClinVarVariant:8427","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:156391","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:159254","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:31650","phenotype":{"types":[{"id":"HP:0001822","label":"Hallux valgus"}]}},{"entity":"AQTL:20631","phenotype":{"types":[{"id":"AQTLTrait:1112","label":"Withers height"}]}},{"entity":"ClinVarVariant:94585","phenotype":{"types":[{"id":"HP:0002948","label":"Vertebral fusion"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00018782-WBRNAi00099196","phenotype":{"types":[{"id":"WBPhenotype:0000961","label":"pattern of transgene expression variant"}]}},{"entity":"ClinVarVariant:159248","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"ClinVarVariant:160328","phenotype":{"types":[{"id":"HP:0001642","label":"Pulmonic stenosis"}]}},{"entity":"MGI:3832569","phenotype":{"types":[{"id":"MP:0006057","label":"decreased vascular endothelial cell number"}]}},{"entity":"ClinVarVariant:39111","phenotype":{"types":[{"id":"HP:0002721","label":"Immunodeficiency"}]}},{"entity":"ClinVarVariant:9106","phenotype":{"types":[{"id":"HP:0100615","label":"Ovarian neoplasm"}]}},{"entity":"ClinVarVariant:24697","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"MGI:1889550","phenotype":{"types":[{"id":"HP:0003826","label":"Stillbirth"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006768-WBRNAi00071339","phenotype":{"types":[{"id":"WBPhenotype:0000961","label":"pattern of transgene expression variant"}]}},{"entity":"ClinVarVariant:67947","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:53687","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:210474","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:49284","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:10935","phenotype":{"types":[{"id":"HP:0002716","label":"Lymphadenopathy"}]}},{"entity":"ClinVarVariant:13080","phenotype":{"types":[{"id":"HP:0002893","label":"Pituitary adenoma"}]}},{"entity":"_:genid1976017","phenotype":{"types":[{"id":"ZP:0003327","label":"abnormal(ly) disrupted cerebellum development"}]}},{"entity":"ClinVarVariant:189613","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"FlyBase:FBal0199281","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:156327","phenotype":{"types":[{"id":"HP:0006530","label":"Interstitial pulmonary disease"}]}},{"entity":"ClinVarVariant:11352","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"ClinVarVariant:102703","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:40512","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"ClinVarVariant:6433","phenotype":{"types":[{"id":"HP:0001939","label":"Abnormality of metabolism/homeostasis"}]}},{"entity":"ClinVarVariant:49241","phenotype":{"types":[{"id":"HP:0002103","label":"Abnormality of the pleura"}]}},{"entity":"ClinVarVariant:135779","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:56679","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:42900","phenotype":{"types":[{"id":"HP:0003128","label":"Lactic acidosis"}]}},{"entity":"ClinVarVariant:1175","phenotype":{"types":[{"id":"HP:0000013","label":"Hypoplasia of the uterus"}]}},{"entity":"ClinVarVariant:374","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"MGI:3709886","phenotype":{"types":[{"id":"HP:0011014","label":"Abnormal glucose homeostasis"}]}},{"entity":"ClinVarVariant:159181","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"dbSNP:rs29026584","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:65536","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:210471","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:53861","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:29690","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:3231","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"dbSNP:rs1768208","phenotype":{"types":[{"id":"HP:0000658","label":"Eyelid apraxia"}]}},{"entity":"ClinVarVariant:190356","phenotype":{"types":[{"id":"HP:0002493","label":"Upper motor neuron dysfunction"}]}},{"entity":"ClinVarVariant:5353","phenotype":{"types":[{"id":"HP:0001871","label":"Abnormality of blood and blood-forming tissues"}]}},{"entity":"ClinVarVariant:188802","phenotype":{"types":[{"id":"HP:0002487","label":"Hyperkinesis"}]}},{"entity":"ClinVarVariant:49761","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:30471","phenotype":{"types":[{"id":"HP:0004348","label":"Abnormality of bone mineral density"}]}},{"entity":"ClinVarVariant:36032","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-980526-332-ZDB-MRPHLNO-041217-12-ZDB-MRPHLNO-041217-13","phenotype":{"types":[{"id":"ZP:0000027","label":"abnormal(ly) decreased length post-vent region"}]}},{"entity":"ClinVarVariant:7235","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:54083","phenotype":{"types":[{"id":"HP:0000966","label":"Hypohidrosis"}]}},{"entity":"ClinVarVariant:97711","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"ClinVarVariant:159931","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:13090","phenotype":{"types":[{"id":"HP:0002893","label":"Pituitary adenoma"}]}},{"entity":"ClinVarVariant:8120","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:24856","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ClinVarVariant:5825","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:50191","phenotype":{"types":[{"id":"HP:0006772","label":"Renal angiomyolipoma"}]}},{"entity":"ClinVarVariant:2131","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:11161","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"MGI:3579497","phenotype":{"types":[{"id":"GO:0030154PHENOTYPE","label":"cell differentiation phenotype"}]}},{"entity":"AQTL:46070","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:136410","phenotype":{"types":[{"id":"HP:0200040","label":"Epidermoid cyst"}]}},{"entity":"AQTL:5491","phenotype":{"types":[{"id":"AQTLTrait:479","label":"Basophil number"}]}},{"entity":"dbSNP:rs110865743","phenotype":{"types":[{"id":"AQTLTrait:1004","label":"Somatic cell count"}]}},{"entity":"ClinVarVariant:198054","phenotype":{"types":[{"id":"HP:0011712","label":"Right bundle branch block"}]}},{"entity":"ClinVarVariant:13445","phenotype":{"types":[{"id":"HP:0001269","label":"Hemiparesis"}]}},{"entity":"ClinVarVariant:102806","phenotype":{"types":[{"id":"HP:0003231","label":"Hypertyrosinemia"}]}},{"entity":"ClinVarVariant:2657","phenotype":{"types":[{"id":"HP:0006101","label":"Finger syndactyly"}]}},{"entity":"ClinVarVariant:42307","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"ClinVarVariant:158297","phenotype":{"types":[{"id":"HP:0009911","label":"Abnormality of the temporal bone"}]}},{"entity":"ClinVarVariant:128211","phenotype":{"types":[{"id":"HP:0002488","label":"Acute leukemia"}]}},{"entity":"ClinVarVariant:9290","phenotype":{"types":[{"id":"HP:0002063","label":"Rigidity"}]}},{"entity":"ClinVarVariant:188893","phenotype":{"types":[{"id":"HP:0001947","label":"Renal tubular acidosis"}]}},{"entity":"ClinVarVariant:16788","phenotype":{"types":[{"id":"HP:0001274","label":"Agenesis of corpus callosum"}]}},{"entity":"MGI:2384513","phenotype":{"types":[{"id":"MP:0013184","label":"hemorrhagic ascites"}]}},{"entity":"AQTL:50226","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004460-WBRNAi00085472","phenotype":{"types":[{"id":"WBPhenotype:0001948","label":"diakinesis progression during oogenesis variant"}]}},{"entity":"ClinVarVariant:159180","phenotype":{"types":[{"id":"HP:0011951","label":"Aspiration pneumonia"}]}},{"entity":"FlyBase:FBal0040484","phenotype":{"types":[{"id":"FBbt:00004510PHENOTYPE","label":"Drosophila ommatidium phenotype"}]}},{"entity":"ClinVarVariant:8942","phenotype":{"types":[{"id":"HP:0100843","label":"Glioblastoma"}]}},{"entity":"ClinVarVariant:10100","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"MGI:3722325","phenotype":{"types":[{"id":"HP:0010772","label":"Anomalous pulmonary venous return"}]}},{"entity":"ClinVarVariant:49728","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:192299","phenotype":{"types":[{"id":"HP:0030034","label":"Diffuse glomerular basement membrane lamellation"}]}},{"entity":"ClinVarVariant:21101","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"ClinVarVariant:101229","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:10624","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"ClinVarVariant:12870","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:53975","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:6121","phenotype":{"types":[{"id":"HP:0003537","label":"Hypouricemia"}]}},{"entity":"MGI:1856173","phenotype":{"types":[{"id":"MP:0006030","label":"abnormal otic vesicle development"}]}},{"entity":"MGI:1857278","phenotype":{"types":[{"id":"HP:0000110","label":"Renal dysplasia"}]}},{"entity":"ClinVarVariant:212733","phenotype":{"types":[{"id":"HP:0100783","label":"Breast aplasia"}]}},{"entity":"ClinVarVariant:1902","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"ClinVarVariant:186916","phenotype":{"types":[{"id":"HP:0002858","label":"Meningioma"}]}},{"entity":"ClinVarVariant:94841","phenotype":{"types":[{"id":"HP:0003713","label":"Muscle fiber necrosis"}]}},{"entity":"ZFIN:ZDB-ALT-980520-19","phenotype":{"types":[{"id":"ZP:0000406","label":"abnormal(ly) quality sensory system"}]}},{"entity":"ClinVarVariant:9591","phenotype":{"types":[{"id":"HP:0002401","label":"Stroke-like episodes"}]}},{"entity":"ClinVarVariant:65859","phenotype":{"types":[{"id":"HP:0001182","label":"Tapered finger"}]}},{"entity":"ClinVarVariant:83189","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"ClinVarVariant:41057","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:64708","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"ClinVarVariant:209","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:182730","phenotype":{"types":[{"id":"HP:0003189","label":"Long nose"}]}},{"entity":"ClinVarVariant:41023","phenotype":{"types":[{"id":"HP:0009027","label":"Foot dorsiflexor weakness"}]}},{"entity":"ClinVarVariant:127338","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"ClinVarVariant:49450","phenotype":{"types":[{"id":"HP:0009719","label":"Hypomelanotic macule"}]}},{"entity":"ClinVarVariant:190346","phenotype":{"types":[{"id":"HP:0002493","label":"Upper motor neuron dysfunction"}]}},{"entity":"ClinVarVariant:3852","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"MGI:3779080","phenotype":{"types":[{"id":"MP:0010955","label":"abnormal respiratory electron transport chain"}]}},{"entity":"ClinVarVariant:216221","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:40563","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:35855","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"MGI:5635433","phenotype":{"types":[{"id":"MP:0004799","label":"increased susceptibility to experimental autoimmune encephalomyelitis"}]}},{"entity":"ClinVarVariant:24381","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"ClinVarVariant:35868","phenotype":{"types":[{"id":"HP:0100027","label":"Recurrent pancreatitis"}]}},{"entity":"ClinVarVariant:127830","phenotype":{"types":[{"id":"HP:0100585","label":"Telangiectasia of the skin"}]}},{"entity":"ClinVarVariant:143704","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ClinVarVariant:194332","phenotype":{"types":[{"id":"HP:0001350","label":"Slurred speech"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006944-WBRNAi00063314","phenotype":{"types":[{"id":"WBPhenotype:0000697","label":"protruding vulva"}]}},{"entity":"ClinVarVariant:3968","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"MGI:2677631","phenotype":{"types":[{"id":"HP:0010831","label":"Impaired proprioception"}]}},{"entity":"ClinVarVariant:4417","phenotype":{"types":[{"id":"HP:0002200","label":"Pseudobulbar signs"}]}},{"entity":"ClinVarVariant:53996","phenotype":{"types":[{"id":"HP:0010444","label":"Pulmonary insufficiency"}]}},{"entity":"ClinVarVariant:53726","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:25179","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:128201","phenotype":{"types":[{"id":"HP:0002488","label":"Acute leukemia"}]}},{"entity":"ClinVarVariant:207995","phenotype":{"types":[{"id":"HP:0002148","label":"Hypophosphatemia"}]}},{"entity":"MGI:5447471","phenotype":{"types":[{"id":"HP:0003097","label":"Short femur"}]}},{"entity":"ClinVarVariant:194115","phenotype":{"types":[{"id":"HP:0000232","label":"Everted lower lip vermilion"}]}},{"entity":"FlyBase:FBal0245644","phenotype":{"types":[{"id":"FBbt:00005378PHENOTYPE","label":"wing margin phenotype"}]}},{"entity":"FlyBase:FBal0125399","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:159093","phenotype":{"types":[{"id":"HP:0009937","label":"Facial hirsutism"}]}},{"entity":"ClinVarVariant:36093","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:209200","phenotype":{"types":[{"id":"HP:0002126","label":"Polymicrogyria"}]}},{"entity":"ClinVarVariant:12662","phenotype":{"types":[{"id":"HP:0000963","label":"Thin skin"}]}},{"entity":"ClinVarVariant:17247","phenotype":{"types":[{"id":"HP:0000772","label":"Abnormality of the ribs"}]}},{"entity":"ClinVarVariant:1589","phenotype":{"types":[{"id":"HP:0000140","label":"Abnormality of the menstrual cycle"}]}},{"entity":"ClinVarVariant:143113","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:6982","phenotype":{"types":[{"id":"HP:0002553","label":"Highly arched eyebrow"}]}},{"entity":"MGI:3711006","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:60534","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:143554","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"ClinVarVariant:56304","phenotype":{"types":[{"id":"HP:0001562","label":"Oligohydramnios"}]}},{"entity":"ClinVarVariant:10771","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:135886","phenotype":{"types":[{"id":"HP:0200042","label":"Skin ulcer"}]}},{"entity":"ClinVarVariant:101395","phenotype":{"types":[{"id":"HP:0005293","label":"Venous insufficiency"}]}},{"entity":"ClinVarVariant:38580","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"ClinVarVariant:10663","phenotype":{"types":[{"id":"HP:0005542","label":"Prolonged whole-blood clotting time"}]}},{"entity":"FlyBase:FBal0210316","phenotype":{"types":[{"id":"FBbt:00005149PHENOTYPE","label":"ganglion mother cell phenotype"}]}},{"entity":"ClinVarVariant:24412","phenotype":{"types":[{"id":"HP:0011508","label":"Macular hole"}]}},{"entity":"ClinVarVariant:4452","phenotype":{"types":[{"id":"HP:0001947","label":"Renal tubular acidosis"}]}},{"entity":"ClinVarVariant:156058","phenotype":{"types":[{"id":"HP:0002270","label":"Abnormality of the autonomic nervous system"}]}},{"entity":"ClinVarVariant:209163","phenotype":{"types":[{"id":"HP:0011220","label":"Prominent forehead"}]}},{"entity":"ClinVarVariant:7995","phenotype":{"types":[{"id":"HP:0002984","label":"Hypoplasia of the radius"}]}},{"entity":"ClinVarVariant:102626","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:10639","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"MGI:1856088","phenotype":{"types":[{"id":"MP:0006069","label":"abnormal retinal neuronal layer morphology"}]}},{"entity":"ClinVarVariant:7225","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:140867","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:36071","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:40370","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:11034","phenotype":{"types":[{"id":"HP:0001106","label":"Periorbital hyperpigmentation"}]}},{"entity":"ClinVarVariant:17219","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"MGI:3808477","phenotype":{"types":[{"id":"MP:0004920","label":"increased placenta weight"}]}},{"entity":"MGI:2183509","phenotype":{"types":[{"id":"MP:0004411","label":"decreased endocochlear potential"}]}},{"entity":"FlyBase:FBal0294937","phenotype":{"types":[{"id":"FBcv:0000440","label":"chemical sensitive"}]}},{"entity":"MGI:1857225","phenotype":{"types":[{"id":"MP:0004417","label":"decreased cochlear nerve compound action potential"}]}},{"entity":"ClinVarVariant:29700","phenotype":{"types":[{"id":"HP:0005900","label":"Fifth metacarpal with ulnar notch"}]}},{"entity":"ClinVarVariant:13070","phenotype":{"types":[{"id":"HP:0002893","label":"Pituitary adenoma"}]}},{"entity":"ClinVarVariant:21441","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:7179","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050103-13-ZDB-MRPHLNO-120727-1","phenotype":{"types":[{"id":"ZP:0002751","label":"abnormal(ly) hemorrhagic cranial vasculature"}]}},{"entity":"ClinVarVariant:211839","phenotype":{"types":[{"id":"HP:0007359","label":"Focal seizures"}]}},{"entity":"ClinVarVariant:65511","phenotype":{"types":[{"id":"HP:0002066","label":"Gait ataxia"}]}},{"entity":"ClinVarVariant:4465","phenotype":{"types":[{"id":"HP:0000988","label":"Skin rash"}]}},{"entity":"MGI:3852440","phenotype":{"types":[{"id":"MP:0010589","label":"common truncal valve"}]}},{"entity":"ClinVarVariant:195052","phenotype":{"types":[{"id":"HP:0004280","label":"Irregular ossification of hand bones"}]}},{"entity":"ClinVarVariant:56495","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:97701","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"ClinVarVariant:143714","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:2677647","phenotype":{"types":[{"id":"MP:0011088","label":"neonatal lethality, incomplete penetrance"}]}},{"entity":"ClinVarVariant:13396","phenotype":{"types":[{"id":"HP:0001260","label":"Dysarthria"}]}},{"entity":"ClinVarVariant:159973","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"ClinVarVariant:30664","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:31028","phenotype":{"types":[{"id":"HP:0010307","label":"Stridor"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006416-WBRNAi00095532","phenotype":{"types":[{"id":"WBPhenotype:0000402","label":"avoids bacterial lawn"}]}},{"entity":"ClinVarVariant:186867","phenotype":{"types":[{"id":"HP:0002073","label":"Progressive cerebellar ataxia"}]}},{"entity":"ClinVarVariant:11708","phenotype":{"types":[{"id":"HP:0008388","label":"Abnormality of the toenails"}]}},{"entity":"ClinVarVariant:36642","phenotype":{"types":[{"id":"HP:0004308","label":"Ventricular arrhythmia"}]}},{"entity":"ClinVarVariant:8965","phenotype":{"types":[{"id":"HP:0006561","label":"Lipid accumulation in hepatocytes"}]}},{"entity":"ClinVarVariant:25194","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:529","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"ClinVarVariant:156088","phenotype":{"types":[{"id":"HP:0002270","label":"Abnormality of the autonomic nervous system"}]}},{"entity":"ClinVarVariant:6111","phenotype":{"types":[{"id":"HP:0003537","label":"Hypouricemia"}]}},{"entity":"ClinVarVariant:189781","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ClinVarVariant:53484","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:53922","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"_:genid1976433","phenotype":{"types":[{"id":"ZP:0007732","label":"abnormal(ly) decreased amount skeletal muscle cell Z disc"}]}},{"entity":"ClinVarVariant:6718","phenotype":{"types":[{"id":"HP:0100587","label":"Abnormality of the preputium"}]}},{"entity":"ClinVarVariant:35755","phenotype":{"types":[{"id":"HP:0000137","label":"Abnormality of the ovary"}]}},{"entity":"ClinVarVariant:50081","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:1216","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"ClinVarVariant:137994","phenotype":{"types":[{"id":"HP:0000707","label":"Abnormality of the nervous system"}]}},{"entity":"ClinVarVariant:7142","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:10462","phenotype":{"types":[{"id":"HP:0003651","label":"Foam cells"}]}},{"entity":"ClinVarVariant:12063","phenotype":{"types":[{"id":"HP:0008321","label":"Reduced factor X activity"}]}},{"entity":"ClinVarVariant:2468","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:95939","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:39712","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004197-WBRNAi00007235","phenotype":{"types":[{"id":"WBPhenotype:0001263","label":"peroxisome morphology variant"}]}},{"entity":"ClinVarVariant:65124","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:215578","phenotype":{"types":[{"id":"HP:0008348","label":"Immunoglobulin IgG2 deficiency"}]}},{"entity":"ClinVarVariant:156238","phenotype":{"types":[{"id":"HP:0000496","label":"Abnormality of eye movement"}]}},{"entity":"ClinVarVariant:10279","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"AQTL:49858","phenotype":{"types":[{"id":"AQTLTrait:1004","label":"Somatic cell count"}]}},{"entity":"ClinVarVariant:48885","phenotype":{"types":[{"id":"HP:0100764","label":"Lymphangioma"}]}},{"entity":"FlyBase:FBal0236318","phenotype":{"types":[{"id":"FBbt:00000034PHENOTYPE","label":"Drosophila egg phenotype"}]}},{"entity":"ClinVarVariant:634","phenotype":{"types":[{"id":"HP:0004395","label":"Malnutrition"}]}},{"entity":"ClinVarVariant:6094","phenotype":{"types":[{"id":"HP:0006989","label":"Dysplastic corpus callosum"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001093-WBRNAi00026282","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:1932","phenotype":{"types":[{"id":"HP:0006573","label":"Acute hepatic steatosis"}]}},{"entity":"ClinVarVariant:2239","phenotype":{"types":[{"id":"HP:0001287","label":"Meningitis"}]}},{"entity":"ClinVarVariant:2020","phenotype":{"types":[{"id":"HP:0000992","label":"Cutaneous photosensitivity"}]}},{"entity":"ClinVarVariant:42391","phenotype":{"types":[{"id":"HP:0100775","label":"Dural ectasia"}]}},{"entity":"ClinVarVariant:48971","phenotype":{"types":[{"id":"HP:0009594","label":"Retinal hamartoma"}]}},{"entity":"MGI:1857149","phenotype":{"types":[{"id":"MP:0001191","label":"abnormal skin condition"}]}},{"entity":"ClinVarVariant:199656","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"ClinVarVariant:2824","phenotype":{"types":[{"id":"HP:0000297","label":"Facial hypotonia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022042-WBRNAi00081339","phenotype":{"types":[{"id":"WBPhenotype:0001027","label":"nuclear position defective early emb"}]}},{"entity":"ClinVarVariant:53705","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"MGI:4437094","phenotype":{"types":[{"id":"MP:0003059","label":"decreased insulin secretion"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004738-WBRNAi00065884","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:94537","phenotype":{"types":[{"id":"HP:0100595","label":"Camptocormia"}]}},{"entity":"ClinVarVariant:53663","phenotype":{"types":[{"id":"HP:0100651","label":"Type I diabetes mellitus"}]}},{"entity":"ClinVarVariant:136120","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:162048","phenotype":{"types":[{"id":"HP:0009830","label":"Peripheral neuropathy"}]}},{"entity":"ClinVarVariant:49800","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:39534","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:183820","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"MGI:1857227","phenotype":{"types":[{"id":"MP:0001921","label":"reduced fertility"}]}},{"entity":"ClinVarVariant:54030","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"ClinVarVariant:204016","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:2276","phenotype":{"types":[{"id":"HP:0002936","label":"Distal sensory impairment"}]}},{"entity":"ClinVarVariant:25211","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"MGI:2675121","phenotype":{"types":[{"id":"MP:0010979","label":"small ureteric bud"}]}},{"entity":"ClinVarVariant:11544","phenotype":{"types":[{"id":"HP:0006145","label":"Central Y-shaped metacarpal"}]}},{"entity":"ClinVarVariant:38302","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:161353","phenotype":{"types":[{"id":"HP:0001038","label":"Warfarin-induced skin necrosis"}]}},{"entity":"ClinVarVariant:5539","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"MGI:3583735","phenotype":{"types":[{"id":"MP:0000968","label":"abnormal sensory neuron innervation pattern"}]}},{"entity":"ClinVarVariant:11634","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"ZFIN:ZDB-ALT-050916-14","phenotype":{"types":[{"id":"ZP:0000530","label":"abnormal(ly) collapsed dorsal aorta"}]}},{"entity":"MGI:2156622","phenotype":{"types":[{"id":"MP:0001853","label":"heart inflammation"}]}},{"entity":"MGI:3578655","phenotype":{"types":[{"id":"GO:0021636PHENOTYPE","label":"trigeminal nerve morphogenesis phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004915-WBRNAi00075315","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:41172","phenotype":{"types":[{"id":"HP:0003162","label":"Fasting hypoglycemia"}]}},{"entity":"FlyBase:FBal0190540","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:5425","phenotype":{"types":[{"id":"HP:0004927","label":"Pulmonary artery dilatation"}]}},{"entity":"ClinVarVariant:36305","phenotype":{"types":[{"id":"HP:0001025","label":"Urticaria"}]}},{"entity":"ClinVarVariant:158359","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:53265","phenotype":{"types":[{"id":"HP:0011850","label":"Parotitis"}]}},{"entity":"ClinVarVariant:92564","phenotype":{"types":[{"id":"HP:0012702","label":"Tenesmus"}]}},{"entity":"ClinVarVariant:180310","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:212733","phenotype":{"types":[{"id":"HP:0003220","label":"Abnormality of chromosome stability"}]}},{"entity":"ClinVarVariant:17282","phenotype":{"types":[{"id":"HP:0004277","label":"Fractured hand bones"}]}},{"entity":"ClinVarVariant:41078","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:6935","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ZFIN:ZDB-ALT-060602-2","phenotype":{"types":[{"id":"ZP:0006118","label":"abnormal(ly) dilated enterocyte Golgi apparatus"}]}},{"entity":"ClinVarVariant:67937","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:204591","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"MGI:1856893","phenotype":{"types":[{"id":"HP:0012447","label":"Abnormal myelination"}]}},{"entity":"ClinVarVariant:101249","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:49468","phenotype":{"types":[{"id":"HP:0004755","label":"Supraventricular tachycardia"}]}},{"entity":"ClinVarVariant:157677","phenotype":{"types":[{"id":"HP:0008527","label":"Congenital sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:7132","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"MGI:3770133","phenotype":{"types":[{"id":"HP:0000618","label":"Blindness"}]}},{"entity":"ClinVarVariant:210023","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"MGI:2181380","phenotype":{"types":[{"id":"HP:0000029","label":"Testicular atrophy"}]}},{"entity":"ClinVarVariant:215572","phenotype":{"types":[{"id":"HP:0100242","label":"Sarcoma"}]}},{"entity":"ClinVarVariant:101405","phenotype":{"types":[{"id":"HP:0000963","label":"Thin skin"}]}},{"entity":"ClinVarVariant:2145","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"ClinVarVariant:53774","phenotype":{"types":[{"id":"HP:0011109","label":"Chronic sinusitis"}]}},{"entity":"ClinVarVariant:206816","phenotype":{"types":[{"id":"HP:0005484","label":"Postnatal microcephaly"}]}},{"entity":"ClinVarVariant:39442","phenotype":{"types":[{"id":"HP:0007333","label":"Hypoplasia of the frontal lobes"}]}},{"entity":"ClinVarVariant:6050","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:56814","phenotype":{"types":[{"id":"HP:0002676","label":"Cloverleaf skull"}]}},{"entity":"ClinVarVariant:3652","phenotype":{"types":[{"id":"HP:0002028","label":"Chronic diarrhea"}]}},{"entity":"MGI:3512077","phenotype":{"types":[{"id":"MP:0009419","label":"skeletal muscle fibrosis"}]}},{"entity":"ClinVarVariant:4954","phenotype":{"types":[{"id":"HP:0002315","label":"Headache"}]}},{"entity":"ClinVarVariant:101394","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:9219","phenotype":{"types":[{"id":"HP:0011157","label":"Auras"}]}},{"entity":"ClinVarVariant:3861","phenotype":{"types":[{"id":"HP:0000787","label":"Nephrolithiasis"}]}},{"entity":"ZFIN:ZDB-ALT-070309-1","phenotype":{"types":[{"id":"ZP:0010305","label":"abnormal(ly) decreased size atrioventricular canal"}]}},{"entity":"ClinVarVariant:197075","phenotype":{"types":[{"id":"HP:0000431","label":"Wide nasal bridge"}]}},{"entity":"ClinVarVariant:3612","phenotype":{"types":[{"id":"HP:0007819","label":"Presenile cataracts"}]}},{"entity":"ClinVarVariant:11340","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000912-WBRNAi00087983","phenotype":{"types":[{"id":"WBPhenotype:0001171","label":"shortened life span"}]}},{"entity":"ClinVarVariant:101155","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:53995","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:8663","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:10209","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:216067","phenotype":{"types":[{"id":"HP:0009736","label":"Tibial pseudoarthrosis"}]}},{"entity":"ClinVarVariant:211630","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00020051-WBRNAi00095700","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:18336","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:180210","phenotype":{"types":[{"id":"HP:0000974","label":"Hyperextensible skin"}]}},{"entity":"ClinVarVariant:10614","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"WormBase:WBVar00087953","phenotype":{"types":[{"id":"WBPhenotype:0001350","label":"protein phosphorylation increased"}]}},{"entity":"ClinVarVariant:189643","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:2119","phenotype":{"types":[{"id":"HP:0000174","label":"Abnormality of the palate"}]}},{"entity":"MGI:2148547","phenotype":{"types":[{"id":"MP:0006042","label":"increased apoptosis"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-110805-2-ZDB-MRPHLNO-111102-4","phenotype":{"types":[{"id":"ZP:0004922","label":"abnormal(ly) malformed neurohypophysis vasculature"}]}},{"entity":"ClinVarVariant:53748","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:208543","phenotype":{"types":[{"id":"HP:0001344","label":"Absent speech"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019481-WBRNAi00063437","phenotype":{"types":[{"id":"WBPhenotype:0000436","label":"protein subcellular localization variant"}]}},{"entity":"ClinVarVariant:53402","phenotype":{"types":[{"id":"HP:0001948","label":"Alkalosis"}]}},{"entity":"ClinVarVariant:35860","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:50235","phenotype":{"types":[{"id":"HP:0000322","label":"Short philtrum"}]}},{"entity":"ClinVarVariant:1068","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:127727","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:53640","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"MGI:1856656","phenotype":{"types":[{"id":"HP:0001254","label":"Lethargy"}]}},{"entity":"ClinVarVariant:46464","phenotype":{"types":[{"id":"HP:0000738","label":"Hallucinations"}]}},{"entity":"ClinVarVariant:54091","phenotype":{"types":[{"id":"HP:0011034","label":"Amyloidosis"}]}},{"entity":"ClinVarVariant:3221","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:159157","phenotype":{"types":[{"id":"HP:0100627","label":"Displacement of the external urethral meatus"}]}},{"entity":"ZFIN:ZDB-ALT-011017-8","phenotype":{"types":[{"id":"ZP:0013971","label":"abnormal(ly) disrupted caudal fin morphogenesis"}]}},{"entity":"ClinVarVariant:53714","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:16932","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:3157","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:216196","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:194808","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:101213","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"ClinVarVariant:46601","phenotype":{"types":[{"id":"HP:0003327","label":"Axial muscle weakness"}]}},{"entity":"ClinVarVariant:2139","phenotype":{"types":[{"id":"HP:0000089","label":"Renal hypoplasia"}]}},{"entity":"FlyBase:FBal0135890","phenotype":{"types":[{"id":"FBcv:0000411","label":"visual behavior defective"}]}},{"entity":"ClinVarVariant:126827","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:120272","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:200129","phenotype":{"types":[{"id":"HP:0001166","label":"Arachnodactyly"}]}},{"entity":"ClinVarVariant:198695","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:3773644","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"ClinVarVariant:53866","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:161355","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:13372","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004953-WBRNAi00038543","phenotype":{"types":[{"id":"WBPhenotype:0000034","label":"embryonic polarity variant"}]}},{"entity":"ClinVarVariant:56485","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:53446","phenotype":{"types":[{"id":"HP:0006538","label":"Recurrent bronchopulmonary infections"}]}},{"entity":"WormBase:WBVar00251819","phenotype":{"types":[{"id":"WBPhenotype:0000142","label":"cell stress response variant"}]}},{"entity":"ClinVarVariant:24866","phenotype":{"types":[{"id":"HP:0001636","label":"Tetralogy of Fallot"}]}},{"entity":"ClinVarVariant:4274","phenotype":{"types":[{"id":"HP:0000235","label":"Abnormality of the fontanelles or cranial sutures"}]}},{"entity":"ClinVarVariant:31695","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"FlyBase:FBal0151492","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:35875","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:36091","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"MGI:5438282","phenotype":{"types":[{"id":"MP:0005169","label":"abnormal male meiosis"}]}},{"entity":"dbSNP:rs109463474","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:21170","phenotype":{"types":[{"id":"HP:0001518","label":"Small for gestational age"}]}},{"entity":"MGI:3790794","phenotype":{"types":[{"id":"MP:0001302","label":"eyelids open at birth"}]}},{"entity":"ClinVarVariant:189730","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:182720","phenotype":{"types":[{"id":"HP:0003189","label":"Long nose"}]}},{"entity":"ClinVarVariant:53226","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:12995","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:53963","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:194320","phenotype":{"types":[{"id":"HP:0100689","label":"Decreased corneal thickness"}]}},{"entity":"ClinVarVariant:93888","phenotype":{"types":[{"id":"HP:0000311","label":"Round face"}]}},{"entity":"FlyBase:FBal0210205","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"MGI:1857326","phenotype":{"types":[{"id":"HP:0002251","label":"Aganglionic megacolon"}]}},{"entity":"ClinVarVariant:10350","phenotype":{"types":[{"id":"HP:0006380","label":"Knee flexion contracture"}]}},{"entity":"ClinVarVariant:53209","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"FlyBase:FBal0039464","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:11075","phenotype":{"types":[{"id":"HP:0100709","label":"Reduction of oligodendroglia"}]}},{"entity":"ClinVarVariant:10138","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"ClinVarVariant:39425","phenotype":{"types":[{"id":"HP:0003127","label":"Hypocalciuria"}]}},{"entity":"ClinVarVariant:35848","phenotype":{"types":[{"id":"HP:0006516","label":"Hypersensitivity pneumonitis"}]}},{"entity":"NCBIGene:791085","phenotype":{"types":[{"id":"HP:0000337","label":"Broad forehead"}]}},{"entity":"ClinVarVariant:49939","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"ClinVarVariant:30528","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"dbSNP:rs1819084","phenotype":{"types":[{"id":"HP:0002028","label":"Chronic diarrhea"}]}},{"entity":"FlyBase:FBal0219831","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:10868","phenotype":{"types":[{"id":"HP:0008572","label":"External ear malformation"}]}},{"entity":"ClinVarVariant:8267","phenotype":{"types":[{"id":"HP:0001082","label":"Cholecystitis"}]}},{"entity":"FlyBase:FBal0177466","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:11228","phenotype":{"types":[{"id":"HP:0001685","label":"Myocardial fibrosis"}]}},{"entity":"ClinVarVariant:159936","phenotype":{"types":[{"id":"HP:0040082","label":"Happy demeanor"}]}},{"entity":"ClinVarVariant:100921","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:45126","phenotype":{"types":[{"id":"HP:0002047","label":"Malignant hyperthermia"}]}},{"entity":"ClinVarVariant:12816","phenotype":{"types":[{"id":"HP:0008417","label":"Vertebral hypoplasia"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-070410-133-ZDB-MRPHLNO-130620-1","phenotype":{"types":[{"id":"ZP:0008698","label":"abnormal(ly) increased accumulation nucleate erythrocyte towards dorsal aorta"}]}},{"entity":"ClinVarVariant:127459","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"FlyBase:FBal0205974","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:163152","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:30999","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:101142","phenotype":{"types":[{"id":"HP:0000490","label":"Deeply set eye"}]}},{"entity":"FlyBase:FBal0198779","phenotype":{"types":[{"id":"FBbt:00005169PHENOTYPE","label":"Drosophila trichogen cell phenotype"}]}},{"entity":"ClinVarVariant:15644","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:210300","phenotype":{"types":[{"id":"HP:0000457","label":"Depressed nasal ridge"}]}},{"entity":"MGI:1857444","phenotype":{"types":[{"id":"GO:0045765PHENOTYPE","label":"regulation of angiogenesis phenotype"}]}},{"entity":"ClinVarVariant:49232","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:21410","phenotype":{"types":[{"id":"HP:0002069","label":"Generalized tonic-clonic seizures"}]}},{"entity":"ClinVarVariant:39727","phenotype":{"types":[{"id":"HP:0002910","label":"Elevated hepatic transaminases"}]}},{"entity":"ClinVarVariant:49105","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:53985","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:140517","phenotype":{"types":[{"id":"HP:0004540","label":"Congenital, generalized hypertrichosis"}]}},{"entity":"MGI:1933758","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:40522","phenotype":{"types":[{"id":"HP:0000276","label":"Long face"}]}},{"entity":"ClinVarVariant:4234","phenotype":{"types":[{"id":"HP:0010935","label":"Abnormality of the upper urinary tract"}]}},{"entity":"ClinVarVariant:36294","phenotype":{"types":[{"id":"HP:0000832","label":"Primary hypothyroidism"}]}},{"entity":"ClinVarVariant:65623","phenotype":{"types":[{"id":"HP:0001159","label":"Syndactyly"}]}},{"entity":"ClinVarVariant:8379","phenotype":{"types":[{"id":"HP:0003097","label":"Short femur"}]}},{"entity":"ClinVarVariant:3323","phenotype":{"types":[{"id":"HP:0008998","label":"Pectoralis hypoplasia"}]}},{"entity":"ClinVarVariant:41190","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:188880","phenotype":{"types":[{"id":"HP:0002835","label":"Aspiration"}]}},{"entity":"ClinVarVariant:36092","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:126948","phenotype":{"types":[{"id":"HP:0002435","label":"Meningocele"}]}},{"entity":"_:genid1972400","phenotype":{"types":[{"id":"ZP:0003234","label":"abnormal(ly) disrupted glomerular filtration"}]}},{"entity":"MGI:4361278","phenotype":{"types":[{"id":"HP:0003081","label":"Increased urinary potassium"}]}},{"entity":"ClinVarVariant:67539","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:53704","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"FlyBase:FBal0202908","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"MGI:1856241","phenotype":{"types":[{"id":"HP:0000134","label":"Female hypogonadism"}]}},{"entity":"WormBase:WBVar00144142","phenotype":{"types":[{"id":"WBPhenotype:0000229","label":"small"}]}},{"entity":"ClinVarVariant:210437","phenotype":{"types":[{"id":"HP:0005599","label":"Hypopigmentation of hair"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011043-WBRNAi00071240","phenotype":{"types":[{"id":"WBPhenotype:0001425","label":"receptor mediated endocytosis defective"}]}},{"entity":"MGI:3528447","phenotype":{"types":[{"id":"HP:0003138","label":"Increased blood urea nitrogen (BUN)"}]}},{"entity":"AQTL:37488","phenotype":{"types":[{"id":"AQTLTrait:1310","label":"Rabies antibody titer"}]}},{"entity":"ClinVarVariant:49163","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00020347-WBRNAi00072072","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:7178","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:45358","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"MGI:3581891","phenotype":{"types":[{"id":"MP:0004560","label":"abnormal chorionic plate morphology"}]}},{"entity":"ClinVarVariant:91610","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:30207","phenotype":{"types":[{"id":"HP:0011682","label":"Perimembranous ventricular septal defect"}]}},{"entity":"ClinVarVariant:210299","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007400-WBRNAi00080157","phenotype":{"types":[{"id":"ZP:0000676","label":"abnormal(ly) increased rate cell proliferation"}]}},{"entity":"FlyBase:FBal0258532","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:21168","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:158731","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:4889","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:3772","phenotype":{"types":[{"id":"HP:0001022","label":"Albinism"}]}},{"entity":"ClinVarVariant:49905","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:68266","phenotype":{"types":[{"id":"HP:0030273","label":"Reduced red cell adenosine deaminase activity"}]}},{"entity":"ClinVarVariant:5626","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:2446","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:9666","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:135716","phenotype":{"types":[{"id":"HP:0007649","label":"Congenital hypertrophy of retinal pigment epithelium"}]}},{"entity":"ClinVarVariant:190195","phenotype":{"types":[{"id":"HP:0002282","label":"Heterotopia"}]}},{"entity":"ClinVarVariant:42750","phenotype":{"types":[{"id":"HP:0002067","label":"Bradykinesia"}]}},{"entity":"ClinVarVariant:4335","phenotype":{"types":[{"id":"HP:0000751","label":"Personality changes"}]}},{"entity":"ClinVarVariant:204258","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:135754","phenotype":{"types":[{"id":"HP:0012539","label":"Non-Hodgkin lymphoma"}]}},{"entity":"MGI:1934195","phenotype":{"types":[{"id":"MP:0011089","label":"perinatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:35822","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"ClinVarVariant:101128","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"MGI:1856223","phenotype":{"types":[{"id":"HP:0000925","label":"Abnormality of the vertebral column"}]}},{"entity":"MGI:3848796","phenotype":{"types":[{"id":"MP:0001606","label":"impaired hematopoiesis"}]}},{"entity":"ClinVarVariant:13540","phenotype":{"types":[{"id":"HP:0001873","label":"Thrombocytopenia"}]}},{"entity":"dbSNP:rs110180463","phenotype":{"types":[{"id":"AQTLTrait:1289","label":"Milk beta-lactoglobulin protein content"}]}},{"entity":"ZFIN:ZDB-ALT-011017-8","phenotype":{"types":[{"id":"ZP:0003184","label":"abnormal(ly) aplastic dorsal longitudinal anastomotic vessel"}]}},{"entity":"MGI:2182093","phenotype":{"types":[{"id":"HP:0003323","label":"Progressive muscle weakness"}]}},{"entity":"ClinVarVariant:177941","phenotype":{"types":[{"id":"HP:0006579","label":"Prolonged neonatal jaundice"}]}},{"entity":"AQTL:5527","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:132740","phenotype":{"types":[{"id":"HP:0001578","label":"Hypercortisolism"}]}},{"entity":"ClinVarVariant:101400","phenotype":{"types":[{"id":"HP:0000790","label":"Hematuria"}]}},{"entity":"ClinVarVariant:65771","phenotype":{"types":[{"id":"HP:0002013","label":"Vomiting"}]}},{"entity":"ClinVarVariant:101174","phenotype":{"types":[{"id":"HP:0100718","label":"Uterine rupture"}]}},{"entity":"FlyBase:FBal0058990","phenotype":{"types":[{"id":"FBbt:00004508PHENOTYPE","label":"eye phenotype"}]}},{"entity":"ClinVarVariant:21502","phenotype":{"types":[{"id":"HP:0001374","label":"Congenital hip dislocation"}]}},{"entity":"ClinVarVariant:100735","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:186986","phenotype":{"types":[{"id":"HP:0002858","label":"Meningioma"}]}},{"entity":"ClinVarVariant:190262","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:56575","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"ClinVarVariant:181737","phenotype":{"types":[{"id":"HP:0009909","label":"Uplifted earlobe"}]}},{"entity":"ClinVarVariant:39095","phenotype":{"types":[{"id":"HP:0030148","label":"Heart murmur"}]}},{"entity":"ClinVarVariant:211726","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:53912","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:10184","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:56603","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:24285","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"ClinVarVariant:189633","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:25330","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:38497","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"MGI:2387580","phenotype":{"types":[{"id":"MP:0002896","label":"abnormal bone mineralization"}]}},{"entity":"ClinVarVariant:36082","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:193484","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"FlyBase:FBal0213151","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:42357","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"ClinVarVariant:6929","phenotype":{"types":[{"id":"HP:0000660","label":"Lipemia retinalis"}]}},{"entity":"ClinVarVariant:132708","phenotype":{"types":[{"id":"HP:0100242","label":"Sarcoma"}]}},{"entity":"AQTL:34784","phenotype":{"types":[{"id":"AQTLTrait:1326","label":"Milk pentadecylic acid percentage"}]}},{"entity":"ClinVarVariant:211636","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"ClinVarVariant:49721","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:10858","phenotype":{"types":[{"id":"HP:0001290","label":"Generalized hypotonia"}]}},{"entity":"ClinVarVariant:21458","phenotype":{"types":[{"id":"HP:0002511","label":"Alzheimer disease"}]}},{"entity":"MGI:4459519","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:12985","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:49995","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"ClinVarVariant:99928","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:67700","phenotype":{"types":[{"id":"HP:0006682","label":"Ventricular extrasystoles"}]}},{"entity":"ClinVarVariant:17093","phenotype":{"types":[{"id":"HP:0100615","label":"Ovarian neoplasm"}]}},{"entity":"MGI:3611770","phenotype":{"types":[{"id":"MP:0004043","label":"abnormal pH regulation"}]}},{"entity":"ClinVarVariant:10604","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"ClinVarVariant:159928","phenotype":{"types":[{"id":"HP:0001939","label":"Abnormality of metabolism/homeostasis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00009365-WBRNAi00002028","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:135765","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:67966","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:38752","phenotype":{"types":[{"id":"HP:0010741","label":"Edema of the lower limbs"}]}},{"entity":"ClinVarVariant:190261","phenotype":{"types":[{"id":"HP:0100699","label":"Scarring"}]}},{"entity":"ClinVarVariant:215580","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:15443","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"ClinVarVariant:143754","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ClinVarVariant:53204","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:39769","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:204046","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:53564","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"MGI:2152962","phenotype":{"types":[{"id":"MP:0003984","label":"embryonic growth retardation"}]}},{"entity":"ClinVarVariant:4800","phenotype":{"types":[{"id":"HP:0002754","label":"Osteomyelitis"}]}},{"entity":"ClinVarVariant:68716","phenotype":{"types":[{"id":"HP:0007109","label":"Periventricular cysts"}]}},{"entity":"ClinVarVariant:126966","phenotype":{"types":[{"id":"HP:0009713","label":"Spinal hemangioblastoma"}]}},{"entity":"ClinVarVariant:158339","phenotype":{"types":[{"id":"HP:0000343","label":"Long philtrum"}]}},{"entity":"ClinVarVariant:18035","phenotype":{"types":[{"id":"HP:0004850","label":"Recurrent deep vein thrombosis"}]}},{"entity":"ClinVarVariant:94804","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:188862","phenotype":{"types":[{"id":"HP:0002487","label":"Hyperkinesis"}]}},{"entity":"ClinVarVariant:12799","phenotype":{"types":[{"id":"HP:0000133","label":"Gonadal dysgenesis"}]}},{"entity":"ClinVarVariant:10163","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"ClinVarVariant:30294","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:159097","phenotype":{"types":[{"id":"HP:0005815","label":"Supernumerary ribs"}]}},{"entity":"ClinVarVariant:41245","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"ClinVarVariant:3196","phenotype":{"types":[{"id":"HP:0003411","label":"Proximal femoral metaphyseal irregularity"}]}},{"entity":"ClinVarVariant:13567","phenotype":{"types":[{"id":"HP:0000132","label":"Menorrhagia"}]}},{"entity":"ClinVarVariant:41132","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00077526-WBRNAi00070047","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:3813","phenotype":{"types":[{"id":"HP:0004332","label":"Abnormality of lymphocytes"}]}},{"entity":"ClinVarVariant:53734","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"_:genid1976152","phenotype":{"types":[{"id":"ZP:0001609","label":"abnormal(ly) morphology head"}]}},{"entity":"ClinVarVariant:68264","phenotype":{"types":[{"id":"HP:0002644","label":"Abnormality of pelvic girdle bone morphology"}]}},{"entity":"ClinVarVariant:8542","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:53935","phenotype":{"types":[{"id":"HP:0100512","label":"Vitamin D deficiency"}]}},{"entity":"ClinVarVariant:534","phenotype":{"types":[{"id":"HP:0000597","label":"Ophthalmoparesis"}]}},{"entity":"ClinVarVariant:9177","phenotype":{"types":[{"id":"HP:0000384","label":"Preauricular skin tag"}]}},{"entity":"ClinVarVariant:3684","phenotype":{"types":[{"id":"HP:0001114","label":"Xanthelasma"}]}},{"entity":"ClinVarVariant:94605","phenotype":{"types":[{"id":"HP:0002948","label":"Vertebral fusion"}]}},{"entity":"FlyBase:FBal0203313","phenotype":{"types":[{"id":"FBcv:0000352","label":"partially lethal - majority die"}]}},{"entity":"ClinVarVariant:211625","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"MGI:1861958","phenotype":{"types":[{"id":"MP:0009684","label":"abnormal spinal cord lateral motor column morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001746-WBRNAi00084506","phenotype":{"types":[{"id":"WBPhenotype:0001235","label":"cell division polarity variant"}]}},{"entity":"ClinVarVariant:2074","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:189159","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:1033","phenotype":{"types":[{"id":"HP:0003103","label":"Abnormal cortical bone morphology"}]}},{"entity":"ClinVarVariant:6834","phenotype":{"types":[{"id":"HP:0003422","label":"Vertebral segmentation defect"}]}},{"entity":"ClinVarVariant:2076","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"FlyBase:FBal0260715","phenotype":{"types":[{"id":"FBbt:00100529PHENOTYPE","label":"Drosophila embryonic/larval carpet glial cell phenotype"}]}},{"entity":"ClinVarVariant:7994","phenotype":{"types":[{"id":"HP:0009777","label":"Absent thumb"}]}},{"entity":"dbSNP:rs41649184","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:158353","phenotype":{"types":[{"id":"HP:0000742","label":"Self-mutilation"}]}},{"entity":"ClinVarVariant:21535","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:49711","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:35850","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"MGI:3847254","phenotype":{"types":[{"id":"MP:0008237","label":"abnormal ventral coat pigmentation"}]}},{"entity":"ClinVarVariant:36970","phenotype":{"types":[{"id":"HP:0007925","label":"Lacrimal duct aplasia"}]}},{"entity":"ClinVarVariant:13455","phenotype":{"types":[{"id":"HP:0001269","label":"Hemiparesis"}]}},{"entity":"ClinVarVariant:24427","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"ClinVarVariant:24538","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:6051","phenotype":{"types":[{"id":"HP:0100864","label":"Short femoral neck"}]}},{"entity":"ClinVarVariant:7172","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:197156","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:10756","phenotype":{"types":[{"id":"HP:0009830","label":"Peripheral neuropathy"}]}},{"entity":"ClinVarVariant:24299","phenotype":{"types":[{"id":"HP:0000613","label":"Photophobia"}]}},{"entity":"ClinVarVariant:24458","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:93896","phenotype":{"types":[{"id":"HP:0003236","label":"Elevated serum creatine phosphokinase"}]}},{"entity":"ClinVarVariant:159941","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:12403","phenotype":{"types":[{"id":"HP:0009727","label":"Achromatic retinal patches"}]}},{"entity":"ClinVarVariant:10713","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"dbSNP:rs12294076","phenotype":{"types":[{"id":"HP:0002102","label":"Pleuritis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011944-WBRNAi00072116","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"MGI:5615712","phenotype":{"types":[{"id":"MP:0020001","label":"decreased response to antigen"}]}},{"entity":"ClinVarVariant:67927","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:24498","phenotype":{"types":[{"id":"HP:0000517","label":"Abnormality of the lens"}]}},{"entity":"ClinVarVariant:31879","phenotype":{"types":[{"id":"HP:0001712","label":"Left ventricular hypertrophy"}]}},{"entity":"ClinVarVariant:12880","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:49701","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:54093","phenotype":{"types":[{"id":"HP:0004401","label":"Meconium ileus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00013532-WBRNAi00058395","phenotype":{"types":[{"id":"WBPhenotype:0000056","label":"late larval arrest"}]}},{"entity":"ZFIN:ZDB-ALT-150528-4","phenotype":{"types":[{"id":"ZP:0012747","label":"abnormal(ly) process quality cranial neural crest neural crest cell migration"}]}},{"entity":"ClinVarVariant:197759","phenotype":{"types":[{"id":"HP:0005107","label":"Abnormality of the sacrum"}]}},{"entity":"ClinVarVariant:8711","phenotype":{"types":[{"id":"HP:0001895","label":"Normochromic anemia"}]}},{"entity":"ClinVarVariant:196933","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:31592","phenotype":{"types":[{"id":"HP:0003034","label":"Diaphyseal sclerosis"}]}},{"entity":"ClinVarVariant:6221","phenotype":{"types":[{"id":"HP:0100335","label":"Non-midline cleft lip"}]}},{"entity":"ClinVarVariant:210043","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"MGI:3809665","phenotype":{"types":[{"id":"MP:0004946","label":"abnormal regulatory T cell physiology"}]}},{"entity":"ClinVarVariant:1569","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"_:genid1976482","phenotype":{"types":[{"id":"ZP:0010599","label":"abnormal(ly) position ceratohyal cartilage"}]}},{"entity":"ClinVarVariant:210790","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"MGI:3583779","phenotype":{"types":[{"id":"MP:0012113","label":"decreased inner cell mass proliferation"}]}},{"entity":"ClinVarVariant:56697","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"NCBIGene:1165","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:54033","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:210476","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"ClinVarVariant:204036","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:2236","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"MGI:1857189","phenotype":{"types":[{"id":"MP:0008211","label":"decreased mature B cell number"}]}},{"entity":"ClinVarVariant:35895","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:10110","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"ClinVarVariant:189153","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:36511","phenotype":{"types":[{"id":"HP:0002633","label":"Vasculitis"}]}},{"entity":"ClinVarVariant:135748","phenotype":{"types":[{"id":"HP:0008348","label":"Immunoglobulin IgG2 deficiency"}]}},{"entity":"MGI:3815539","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:5419","phenotype":{"types":[{"id":"HP:0002150","label":"Hypercalciuria"}]}},{"entity":"MGI:2668901","phenotype":{"types":[{"id":"MP:0002655","label":"abnormal keratinocyte morphology"}]}},{"entity":"ClinVarVariant:156349","phenotype":{"types":[{"id":"HP:0000227","label":"Tongue telangiectasia"}]}},{"entity":"ClinVarVariant:159039","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:29639","phenotype":{"types":[{"id":"HP:0000689","label":"Dental malocclusion"}]}},{"entity":"ClinVarVariant:297","phenotype":{"types":[{"id":"HP:0001873","label":"Thrombocytopenia"}]}},{"entity":"dbSNP:rs132692798","phenotype":{"types":[{"id":"AQTLTrait:1327","label":"Milk odd-chain fatty acid percentage"}]}},{"entity":"ClinVarVariant:216944","phenotype":{"types":[{"id":"HP:0002170","label":"Intracranial hemorrhage"}]}},{"entity":"ClinVarVariant:181713","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:53915","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"dbSNP:rs42436295","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:12661","phenotype":{"types":[{"id":"HP:0008981","label":"Calf muscle hypertrophy"}]}},{"entity":"ClinVarVariant:11040","phenotype":{"types":[{"id":"HP:0007411","label":"Hypoplastic-absent sebaceous glands"}]}},{"entity":"ClinVarVariant:143171","phenotype":{"types":[{"id":"HP:0001123","label":"Visual field defect"}]}},{"entity":"ClinVarVariant:53990","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"ClinVarVariant:24866","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"FlyBase:FBal0296742","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007029-WBRNAi00088606","phenotype":{"types":[{"id":"WBPhenotype:0002057","label":"Bacillus thuringiensis toxin hypersensitive"}]}},{"entity":"ClinVarVariant:161357","phenotype":{"types":[{"id":"HP:0000303","label":"Mandibular prognathia"}]}},{"entity":"FlyBase:FBal0204265","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:65606","phenotype":{"types":[{"id":"HP:0001507","label":"Growth abnormality"}]}},{"entity":"ClinVarVariant:53961","phenotype":{"types":[{"id":"HP:0011947","label":"Respiratory tract infection"}]}},{"entity":"ClinVarVariant:135882","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:38742","phenotype":{"types":[{"id":"HP:0000519","label":"Congenital cataract"}]}},{"entity":"ClinVarVariant:41146","phenotype":{"types":[{"id":"HP:0100267","label":"Lip pit"}]}},{"entity":"ClinVarVariant:53803","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:189663","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:24409","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"MGI:2449695","phenotype":{"types":[{"id":"MP:0002563","label":"shortened circadian period"}]}},{"entity":"ClinVarVariant:24611","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:53964","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:189931","phenotype":{"types":[{"id":"HP:0005484","label":"Postnatal microcephaly"}]}},{"entity":"ClinVarVariant:30665","phenotype":{"types":[{"id":"HP:0000230","label":"Gingivitis"}]}},{"entity":"ClinVarVariant:40257","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"MGI:1856209","phenotype":{"types":[{"id":"GO:0021953PHENOTYPE","label":"central nervous system neuron differentiation phenotype"}]}},{"entity":"ClinVarVariant:24512","phenotype":{"types":[{"id":"HP:0000099","label":"Glomerulonephritis"}]}},{"entity":"ClinVarVariant:44811","phenotype":{"types":[{"id":"HP:0009891","label":"Underdeveloped supraorbital ridges"}]}},{"entity":"ClinVarVariant:8870","phenotype":{"types":[{"id":"HP:0002823","label":"Abnormality of the femur"}]}},{"entity":"ClinVarVariant:10156","phenotype":{"types":[{"id":"HP:0005268","label":"Spontaneous abortion"}]}},{"entity":"ClinVarVariant:210476","phenotype":{"types":[{"id":"HP:0003819","label":"Death in childhood"}]}},{"entity":"MGI:4818801","phenotype":{"types":[{"id":"HP:0001899","label":"Increased hematocrit"}]}},{"entity":"ClinVarVariant:10733","phenotype":{"types":[{"id":"HP:0009763","label":"Limb pain"}]}},{"entity":"FlyBase:FBal0102482","phenotype":{"types":[{"id":"FBcv:0000377","label":"female fertile"}]}},{"entity":"AQTL:54943","phenotype":{"types":[{"id":"AQTLTrait:1004","label":"Somatic cell count"}]}},{"entity":"ClinVarVariant:56625","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:6574","phenotype":{"types":[{"id":"HP:0010783","label":"Erythema"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004813-WBRNAi00075001","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:13823","phenotype":{"types":[{"id":"HP:0002164","label":"Nail dysplasia"}]}},{"entity":"ClinVarVariant:195148","phenotype":{"types":[{"id":"HP:0004327","label":"Abnormality of the vitreous humor"}]}},{"entity":"ClinVarVariant:40502","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:135886","phenotype":{"types":[{"id":"HP:0009733","label":"Glioma"}]}},{"entity":"ClinVarVariant:53932","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:49565","phenotype":{"types":[{"id":"HP:0009716","label":"Subependymal nodules"}]}},{"entity":"ClinVarVariant:13658","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"ClinVarVariant:21160","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"MGI:1857872","phenotype":{"types":[{"id":"MP:0008813","label":"decreased common myeloid progenitor cell number"}]}},{"entity":"ClinVarVariant:183748","phenotype":{"types":[{"id":"HP:0100568","label":"Neoplasm of the endocrine system"}]}},{"entity":"ClinVarVariant:50050","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"ClinVarVariant:56475","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:17974","phenotype":{"types":[{"id":"HP:0002613","label":"Biliary cirrhosis"}]}},{"entity":"MGI:1860866","phenotype":{"types":[{"id":"GO:0051209PHENOTYPE","label":"release of sequestered calcium ion into cytosol phenotype"}]}},{"entity":"MGI:3044898","phenotype":{"types":[{"id":"MP:0013716","label":"hypolactation"}]}},{"entity":"ClinVarVariant:216231","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:188863","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"ClinVarVariant:162395","phenotype":{"types":[{"id":"HP:0010819","label":"Atonic seizures"}]}},{"entity":"MGI:3027823","phenotype":{"types":[{"id":"MP:0001929","label":"abnormal gametogenesis"}]}},{"entity":"ClinVarVariant:1075","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"WormBase:WBVar00094804","phenotype":{"types":[{"id":"WBPhenotype:0001059","label":"magnesium chemotaxis defective"}]}},{"entity":"ClinVarVariant:13001","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:4849547","phenotype":{"types":[{"id":"HP:0002213","label":"Fine hair"}]}},{"entity":"ClinVarVariant:143564","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"ClinVarVariant:209010","phenotype":{"types":[{"id":"HP:0100660","label":"Dyskinesia"}]}},{"entity":"ClinVarVariant:210389","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"MGI:3848347","phenotype":{"types":[{"id":"GO:0008584PHENOTYPE","label":"male gonad development phenotype"}]}},{"entity":"ClinVarVariant:24268","phenotype":{"types":[{"id":"HP:0100273","label":"Neoplasm of the colon"}]}},{"entity":"ClinVarVariant:143744","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ClinVarVariant:68490","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001337-WBRNAi00096891","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:132795","phenotype":{"types":[{"id":"HP:0001874","label":"Abnormality of neutrophils"}]}},{"entity":"ClinVarVariant:158349","phenotype":{"types":[{"id":"HP:0009765","label":"Low hanging columella"}]}},{"entity":"ClinVarVariant:65343","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:11642","phenotype":{"types":[{"id":"HP:0006887","label":"Intellectual disability, progressive"}]}},{"entity":"ClinVarVariant:161287","phenotype":{"types":[{"id":"HP:0001084","label":"Corneal arcus"}]}},{"entity":"ClinVarVariant:29790","phenotype":{"types":[{"id":"HP:0003690","label":"Limb muscle weakness"}]}},{"entity":"MGI:2682016","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"MGI:1932294","phenotype":{"types":[{"id":"HP:0012447","label":"Abnormal myelination"}]}},{"entity":"ClinVarVariant:6794","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:24762","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:21252","phenotype":{"types":[{"id":"HP:0000202","label":"Oral cleft"}]}},{"entity":"ClinVarVariant:53933","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:49411","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"MGI:2136432","phenotype":{"types":[{"id":"MP:0001284","label":"absent vibrissae"}]}},{"entity":"dbSNP:rs109445675","phenotype":{"types":[{"id":"AQTLTrait:1130","label":"Udder cleft"}]}},{"entity":"ClinVarVariant:10912","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"FlyBase:FBal0197136","phenotype":{"types":[{"id":"FBcv:0000397","label":"learning defective"}]}},{"entity":"ClinVarVariant:42756","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:36501","phenotype":{"types":[{"id":"HP:0002633","label":"Vasculitis"}]}},{"entity":"ClinVarVariant:101125","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"ClinVarVariant:6834","phenotype":{"types":[{"id":"HP:0000337","label":"Broad forehead"}]}},{"entity":"FlyBase:FBal0206542","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:9162","phenotype":{"types":[{"id":"HP:0011106","label":"Hypovolemia"}]}},{"entity":"ClinVarVariant:692","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:204026","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:1775","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:164883","phenotype":{"types":[{"id":"HP:0000540","label":"Hypermetropia"}]}},{"entity":"ClinVarVariant:10249","phenotype":{"types":[{"id":"HP:0100845","label":"Anaphylactic shock"}]}},{"entity":"ClinVarVariant:53724","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:24448","phenotype":{"types":[{"id":"HP:0200020","label":"Corneal erosion"}]}},{"entity":"ClinVarVariant:43146","phenotype":{"types":[{"id":"HP:0008555","label":"Absent vestibular function"}]}},{"entity":"ClinVarVariant:54021","phenotype":{"types":[{"id":"HP:0005948","label":"Cystic lung disease"}]}},{"entity":"ClinVarVariant:202199","phenotype":{"types":[{"id":"HP:0005257","label":"Thoracic hypoplasia"}]}},{"entity":"ClinVarVariant:24339","phenotype":{"types":[{"id":"HP:0100539","label":"Periorbital edema"}]}},{"entity":"ClinVarVariant:136155","phenotype":{"types":[{"id":"HP:0000582","label":"Upslanted palpebral fissure"}]}},{"entity":"ClinVarVariant:91600","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:50098","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"ZFIN:ZDB-ALT-071108-4","phenotype":{"types":[{"id":"ZP:0005125","label":"abnormal(ly) decreased size swim bladder"}]}},{"entity":"ClinVarVariant:1371","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"ClinVarVariant:56662","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:6540","phenotype":{"types":[{"id":"HP:0200042","label":"Skin ulcer"}]}},{"entity":"ClinVarVariant:210388","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"ClinVarVariant:40726","phenotype":{"types":[{"id":"HP:0000027","label":"Azoospermia"}]}},{"entity":"ClinVarVariant:24996","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:100739","phenotype":{"types":[{"id":"HP:0000484","label":"Hyperopic astigmatism"}]}},{"entity":"ClinVarVariant:189599","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"ClinVarVariant:158080","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:678","phenotype":{"types":[{"id":"HP:0005543","label":"Reduced protein C activity"}]}},{"entity":"ClinVarVariant:159036","phenotype":{"types":[{"id":"HP:0200054","label":"Monodactyly (feet)"}]}},{"entity":"ClinVarVariant:188984","phenotype":{"types":[{"id":"HP:0006887","label":"Intellectual disability, progressive"}]}},{"entity":"ClinVarVariant:6593","phenotype":{"types":[{"id":"HP:0003155","label":"Elevated alkaline phosphatase"}]}},{"entity":"ClinVarVariant:133628","phenotype":{"types":[{"id":"HP:0005425","label":"Recurrent sinopulmonary infections"}]}},{"entity":"ClinVarVariant:217297","phenotype":{"types":[{"id":"HP:0001144","label":"Orbital cyst"}]}},{"entity":"ClinVarVariant:40869","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004873-WBRNAi00037161","phenotype":{"types":[{"id":"WBPhenotype:0000025","label":"blistered"}]}},{"entity":"ClinVarVariant:41095","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:189125","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:6969","phenotype":{"types":[{"id":"HP:0003148","label":"Elevated serum acid phosphatase"}]}},{"entity":"ClinVarVariant:194120","phenotype":{"types":[{"id":"HP:0000657","label":"Oculomotor apraxia"}]}},{"entity":"ClinVarVariant:56314","phenotype":{"types":[{"id":"HP:0001562","label":"Oligohydramnios"}]}},{"entity":"MGI:2679338","phenotype":{"types":[{"id":"MP:0001473","label":"reduced long term potentiation"}]}},{"entity":"ClinVarVariant:56354","phenotype":{"types":[{"id":"HP:0012156","label":"Hemophagocytosis"}]}},{"entity":"ClinVarVariant:7152","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:210259","phenotype":{"types":[{"id":"HP:0002592","label":"Gastric ulcer"}]}},{"entity":"FlyBase:FBal0057699","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:10649","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:101259","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:157613","phenotype":{"types":[{"id":"HP:0000510","label":"Rod-cone dystrophy"}]}},{"entity":"ClinVarVariant:189653","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:210033","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:13343","phenotype":{"types":[{"id":"HP:0008357","label":"Reduced factor XIII activity"}]}},{"entity":"ClinVarVariant:40525","phenotype":{"types":[{"id":"HP:0030084","label":"Clinodactyly"}]}},{"entity":"ClinVarVariant:45358","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"ClinVarVariant:190395","phenotype":{"types":[{"id":"HP:0011100","label":"Intestinal atresia"}]}},{"entity":"MGI:2384087","phenotype":{"types":[{"id":"HP:0040171","label":"Decreased serum testosterone level"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008476-WBRNAi00024985","phenotype":{"types":[{"id":"WBPhenotype:0000054","label":"larval lethal"}]}},{"entity":"AQTL:30584","phenotype":{"types":[{"id":"AQTLTrait:1559","label":"Cell-mediated immune response"}]}},{"entity":"ClinVarVariant:204107","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:127339","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00018156-WBRNAi00087047","phenotype":{"types":[{"id":"WBPhenotype:0000038","label":"exploded through vulva"}]}},{"entity":"FlyBase:FBal0117671","phenotype":{"types":[{"id":"FBcv:0000358","label":"small body"}]}},{"entity":"MGI:1926498","phenotype":{"types":[{"id":"HP:0000962","label":"Hyperkeratosis"}]}},{"entity":"ClinVarVariant:52348","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"MGI:5297555","phenotype":{"types":[{"id":"MP:0001258","label":"decreased body length"}]}},{"entity":"AQTL:14959","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002226-WBRNAi00074011","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:17112","phenotype":{"types":[{"id":"HP:0007759","label":"Opacification of the corneal stroma"}]}},{"entity":"ClinVarVariant:7624","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:4566","phenotype":{"types":[{"id":"HP:0003487","label":"Babinski sign"}]}},{"entity":"ClinVarVariant:41167","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:132684","phenotype":{"types":[{"id":"HP:0000982","label":"Palmoplantar keratoderma"}]}},{"entity":"MGI:2183411","phenotype":{"types":[{"id":"HP:0011805","label":"Abnormality of muscle morphology"}]}},{"entity":"FlyBase:FBal0210631","phenotype":{"types":[{"id":"FBbt:00005179PHENOTYPE","label":"Drosophila macrochaeta phenotype"}]}},{"entity":"ClinVarVariant:11742","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:66001","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:97544","phenotype":{"types":[{"id":"HP:0000999","label":"Pyoderma"}]}},{"entity":"ClinVarVariant:3364","phenotype":{"types":[{"id":"HP:0001012","label":"Multiple lipomas"}]}},{"entity":"MGI:1857711","phenotype":{"types":[{"id":"GO:0007281PHENOTYPE","label":"germ cell development phenotype"}]}},{"entity":"ClinVarVariant:97000","phenotype":{"types":[{"id":"HP:0000012","label":"Urinary urgency"}]}},{"entity":"MGI:3762119","phenotype":{"types":[{"id":"HP:0011018","label":"Abnormality of the cell cycle"}]}},{"entity":"ClinVarVariant:682","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:159807","phenotype":{"types":[{"id":"HP:0000405","label":"Conductive hearing impairment"}]}},{"entity":"ClinVarVariant:16635","phenotype":{"types":[{"id":"HP:0002027","label":"Abdominal pain"}]}},{"entity":"ClinVarVariant:49482","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"ClinVarVariant:68721","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"dbSNP:rs41668337","phenotype":{"types":[{"id":"AQTLTrait:1115","label":"Chest width"}]}},{"entity":"FlyBase:FBal0239202","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:196726","phenotype":{"types":[{"id":"HP:0001030","label":"Fragile skin"}]}},{"entity":"ClinVarVariant:45344","phenotype":{"types":[{"id":"HP:0004808","label":"Acute myeloid leukemia"}]}},{"entity":"AQTL:3668","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:189693","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:53715","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"dbSNP:rs109089392","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"ClinVarVariant:49560","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:54195","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:204076","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:67917","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:5823","phenotype":{"types":[{"id":"HP:0008472","label":"Prominent protruding coccyx"}]}},{"entity":"ClinVarVariant:2656","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:17112","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"dbSNP:rs3800569","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:40522","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"MGI:1857826","phenotype":{"types":[{"id":"MP:0004453","label":"abnormal pterygoid bone morphology"}]}},{"entity":"ClinVarVariant:66473","phenotype":{"types":[{"id":"HP:0007360","label":"Aplasia/Hypoplasia of the cerebellum"}]}},{"entity":"ClinVarVariant:43580","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"MGI:2656537","phenotype":{"types":[{"id":"HP:0001322","label":"Brain very small"}]}},{"entity":"ClinVarVariant:49781","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:31562","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:39479","phenotype":{"types":[{"id":"HP:0000944","label":"Abnormality of the metaphyses"}]}},{"entity":"ClinVarVariant:188339","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:35840","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:39824","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:211909","phenotype":{"types":[{"id":"HP:0007772","label":"Impaired smooth pursuit"}]}},{"entity":"ClinVarVariant:1078","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:127707","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008053-WBRNAi00093392","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"MGI:3772332","phenotype":{"types":[{"id":"MP:0008209","label":"decreased pre-B cell number"}]}},{"entity":"ClinVarVariant:65877","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:31054","phenotype":{"types":[{"id":"HP:0000625","label":"Cleft eyelid"}]}},{"entity":"ClinVarVariant:18337","phenotype":{"types":[{"id":"HP:0009773","label":"Symphalangism affecting the phalanges of the hand"}]}},{"entity":"ClinVarVariant:53397","phenotype":{"types":[{"id":"HP:0005214","label":"Intestinal obstruction"}]}},{"entity":"WormBase:WBVar00089700","phenotype":{"types":[{"id":"WBPhenotype:0000216","label":"cell fate specification variant"}]}},{"entity":"MGI:5691529","phenotype":{"types":[{"id":"HP:0003196","label":"Short nose"}]}},{"entity":"FlyBase:FBal0117901","phenotype":{"types":[{"id":"FBbt:00001055PHENOTYPE","label":"presumptive embryonic/larval nervous system phenotype"}]}},{"entity":"ClinVarVariant:53754","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"MGI:4881474","phenotype":{"types":[{"id":"MP:0002945","label":"abnormal inhibitory postsynaptic currents"}]}},{"entity":"ClinVarVariant:42177","phenotype":{"types":[{"id":"HP:0002110","label":"Bronchiectasis"}]}},{"entity":"ClinVarVariant:101218","phenotype":{"types":[{"id":"HP:0100585","label":"Telangiectasia of the skin"}]}},{"entity":"ClinVarVariant:209131","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:7393","phenotype":{"types":[{"id":"HP:0000135","label":"Hypogonadism"}]}},{"entity":"ClinVarVariant:95639","phenotype":{"types":[{"id":"HP:0009909","label":"Uplifted earlobe"}]}},{"entity":"ClinVarVariant:49771","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:101223","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"ClinVarVariant:10053","phenotype":{"types":[{"id":"HP:0007325","label":"Generalized dystonia"}]}},{"entity":"ClinVarVariant:56402","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:3862","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"_:genid1975835","phenotype":{"types":[{"id":"ZP:0001663","label":"abnormal(ly) increased branchiness motor neuron axon"}]}},{"entity":"ClinVarVariant:24237","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"FlyBase:FBal0268981","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:166813","phenotype":{"types":[{"id":"HP:0010780","label":"Hyperacusis"}]}},{"entity":"ClinVarVariant:181733","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"MGI:3691651","phenotype":{"types":[{"id":"HP:0003330","label":"Abnormal bone structure"}]}},{"entity":"FlyBase:FBal0200319","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:215765","phenotype":{"types":[{"id":"HP:0005562","label":"Multiple renal cysts"}]}},{"entity":"FlyBase:FBal0190677","phenotype":{"types":[{"id":"FBbt:00005378PHENOTYPE","label":"wing margin phenotype"}]}},{"entity":"ClinVarVariant:53650","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:13329","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:54009","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"MGI:5297120","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:7184","phenotype":{"types":[{"id":"HP:0100027","label":"Recurrent pancreatitis"}]}},{"entity":"ClinVarVariant:49286","phenotype":{"types":[{"id":"HP:0009717","label":"Cortical tubers"}]}},{"entity":"ClinVarVariant:101289","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:11707","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:99920","phenotype":{"types":[{"id":"HP:0000289","label":"Broad philtrum"}]}},{"entity":"ClinVarVariant:17229","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1756","phenotype":{"types":[{"id":"ZP:0000212","label":"abnormal(ly) viability whole organism"}]}},{"entity":"ClinVarVariant:156620","phenotype":{"types":[{"id":"HP:0100021","label":"Cerebral palsy"}]}},{"entity":"ClinVarVariant:54067","phenotype":{"types":[{"id":"HP:0011109","label":"Chronic sinusitis"}]}},{"entity":"ClinVarVariant:53736","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"MGI:2179460","phenotype":{"types":[{"id":"MP:0009678","label":"abnormal spinal cord lateral column morphology"}]}},{"entity":"ClinVarVariant:188794","phenotype":{"types":[{"id":"HP:0002015","label":"Dysphagia"}]}},{"entity":"ClinVarVariant:12000","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00020263-WBRNAi00026196","phenotype":{"types":[{"id":"WBPhenotype:0000697","label":"protruding vulva"}]}},{"entity":"ClinVarVariant:68596","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:210780","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:41258","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"ClinVarVariant:4627","phenotype":{"types":[{"id":"HP:0003390","label":"Sensory axonal neuropathy"}]}},{"entity":"ClinVarVariant:21156","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ZFIN:ZDB-ALT-080325-1","phenotype":{"types":[{"id":"ZP:0015389","label":"abnormal(ly) non-functional sperm mitochondrion"}]}},{"entity":"ClinVarVariant:159236","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:30170","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:12672","phenotype":{"types":[{"id":"HP:0000963","label":"Thin skin"}]}},{"entity":"ClinVarVariant:9001","phenotype":{"types":[{"id":"HP:0010971","label":"Absence of Lutheran antigen on erythrocytes"}]}},{"entity":"ClinVarVariant:210789","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"MGI:3576671","phenotype":{"types":[{"id":"HP:0000021","label":"Megacystis"}]}},{"entity":"ClinVarVariant:10758","phenotype":{"types":[{"id":"HP:0000763","label":"Sensory neuropathy"}]}},{"entity":"ClinVarVariant:10063","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:53952","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050913-84-ZDB-MRPHLNO-070713-2","phenotype":{"types":[{"id":"ZP:0007928","label":"abnormal(ly) edematous heart sarcolemma"}]}},{"entity":"ClinVarVariant:66925","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"MGI:2150346","phenotype":{"types":[{"id":"MP:0009039","label":"absent inferior colliculus"}]}},{"entity":"ClinVarVariant:12607","phenotype":{"types":[{"id":"HP:0000474","label":"Thickened nuchal skin fold"}]}},{"entity":"FlyBase:FBal0230895","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:36132","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:180361","phenotype":{"types":[{"id":"HP:0011645","label":"Sinus of Valsalva aneurysm"}]}},{"entity":"ClinVarVariant:11010","phenotype":{"types":[{"id":"HP:0002021","label":"Pyloric stenosis"}]}},{"entity":"ClinVarVariant:9378","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:65730","phenotype":{"types":[{"id":"HP:0000722","label":"Obsessive-compulsive behavior"}]}},{"entity":"MGI:3036704","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"ClinVarVariant:14087","phenotype":{"types":[{"id":"HP:0001712","label":"Left ventricular hypertrophy"}]}},{"entity":"FlyBase:FBal0204597","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:16911","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:53117","phenotype":{"types":[{"id":"HP:0006696","label":"Polymorphic and polytopic ventricular extrasystoles"}]}},{"entity":"ClinVarVariant:56312","phenotype":{"types":[{"id":"HP:0002323","label":"Anencephaly"}]}},{"entity":"ClinVarVariant:24391","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"ClinVarVariant:94001","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:10289","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:6207","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:127348","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"FlyBase:FBal0202458","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:180411","phenotype":{"types":[{"id":"HP:0100749","label":"Chest pain"}]}},{"entity":"ClinVarVariant:200598","phenotype":{"types":[{"id":"HP:0006696","label":"Polymorphic and polytopic ventricular extrasystoles"}]}},{"entity":"ClinVarVariant:53214","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:11819","phenotype":{"types":[{"id":"HP:0000721","label":"Lack of spontaneous play"}]}},{"entity":"AQTL:51680","phenotype":{"types":[{"id":"AQTLTrait:1120","label":"Thurl width"}]}},{"entity":"FlyBase:FBal0124348","phenotype":{"types":[{"id":"FBcv:0000432","label":"mitotic cell cycle defective"}]}},{"entity":"ClinVarVariant:5086","phenotype":{"types":[{"id":"HP:0000666","label":"Horizontal nystagmus"}]}},{"entity":"dbSNP:rs16879552","phenotype":{"types":[{"id":"HP:0005249","label":"Functional intestinal obstruction"}]}},{"entity":"ClinVarVariant:101196","phenotype":{"types":[{"id":"HP:0000387","label":"Absent earlobe"}]}},{"entity":"MGI:4318693","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006366-WBRNAi00086348","phenotype":{"types":[{"id":"WBPhenotype:0000154","label":"reduced brood size"}]}},{"entity":"WormBase:WBVar00143937","phenotype":{"types":[{"id":"WBPhenotype:0000502","label":"right handed roller"}]}},{"entity":"ClinVarVariant:93356","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:55952","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:155982","phenotype":{"types":[{"id":"HP:0200085","label":"Limb tremor"}]}},{"entity":"ClinVarVariant:204102","phenotype":{"types":[{"id":"HP:0000121","label":"Nephrocalcinosis"}]}},{"entity":"MGI:3837125","phenotype":{"types":[{"id":"MP:0005154","label":"increased B cell proliferation"}]}},{"entity":"ClinVarVariant:36122","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:189043","phenotype":{"types":[{"id":"HP:0002967","label":"Cubitus valgus"}]}},{"entity":"ClinVarVariant:167563","phenotype":{"types":[{"id":"HP:0007018","label":"Attention deficit hyperactivity disorder"}]}},{"entity":"ClinVarVariant:216025","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:5973","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"MGI:2156086","phenotype":{"types":[{"id":"MP:0003645","label":"increased pancreatic beta cell number"}]}},{"entity":"ClinVarVariant:25340","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:216143","phenotype":{"types":[{"id":"HP:0001350","label":"Slurred speech"}]}},{"entity":"AQTL:49968","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"MGI:4440831","phenotype":{"types":[{"id":"MP:0011095","label":"embryonic lethality between implantation and placentation, complete penetrance"}]}},{"entity":"WormBase:WBVar00146423","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:7460","phenotype":{"types":[{"id":"HP:0000069","label":"Abnormality of the ureter"}]}},{"entity":"ClinVarVariant:157618","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"ClinVarVariant:10198","phenotype":{"types":[{"id":"HP:0100310","label":"Epidural hemorrhage"}]}},{"entity":"ClinVarVariant:53412","phenotype":{"types":[{"id":"HP:0001948","label":"Alkalosis"}]}},{"entity":"ClinVarVariant:189740","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:12016","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"MGI:4839231","phenotype":{"types":[{"id":"MP:0009977","label":"abnormal cerebellar granule cell migration"}]}},{"entity":"ClinVarVariant:50019","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:829","phenotype":{"types":[{"id":"HP:0000706","label":"Unerupted tooth"}]}},{"entity":"ClinVarVariant:66105","phenotype":{"types":[{"id":"HP:0001742","label":"Nasal obstruction"}]}},{"entity":"ClinVarVariant:10148","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"MGI:3510641","phenotype":{"types":[{"id":"MP:0003081","label":"abnormal soleus morphology"}]}},{"entity":"FlyBase:FBal0190270","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:204066","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:53902","phenotype":{"types":[{"id":"HP:0001082","label":"Cholecystitis"}]}},{"entity":"ClinVarVariant:18427","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00013144-WBRNAi00082701","phenotype":{"types":[{"id":"MP:0002209","label":"decreased germ cell number"}]}},{"entity":"ClinVarVariant:35733","phenotype":{"types":[{"id":"HP:0000934","label":"Chondrocalcinosis"}]}},{"entity":"ClinVarVariant:82630","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:11379","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:56465","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:48762","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:25036","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"ClinVarVariant:24670","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:162009","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:24292","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:189710","phenotype":{"types":[{"id":"HP:0000478","label":"Abnormality of the eye"}]}},{"entity":"AQTL:25469","phenotype":{"types":[{"id":"AQTLTrait:1044","label":"Milk yield"}]}},{"entity":"ClinVarVariant:24488","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:24581","phenotype":{"types":[{"id":"HP:0100586","label":"Aseptic leukocyturia"}]}},{"entity":"ClinVarVariant:183145","phenotype":{"types":[{"id":"HP:0010318","label":"Aplasia/Hypoplasia of the abdominal wall musculature"}]}},{"entity":"ClinVarVariant:49761","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:41939","phenotype":{"types":[{"id":"HP:0003741","label":"Congenital muscular dystrophy"}]}},{"entity":"ClinVarVariant:126837","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001929-WBRNAi00026532","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:97695","phenotype":{"types":[{"id":"HP:0100537","label":"Fasciitis"}]}},{"entity":"ClinVarVariant:139033","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:53744","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:9990","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"MGI:3811233","phenotype":{"types":[{"id":"MP:0000060","label":"delayed bone ossification"}]}},{"entity":"ClinVarVariant:92205","phenotype":{"types":[{"id":"HP:0000131","label":"Uterine leiomyoma"}]}},{"entity":"ClinVarVariant:53973","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:35456","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:55938","phenotype":{"types":[{"id":"HP:0006887","label":"Intellectual disability, progressive"}]}},{"entity":"ClinVarVariant:189683","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:143543","phenotype":{"types":[{"id":"HP:0010521","label":"Gait apraxia"}]}},{"entity":"ClinVarVariant:210299","phenotype":{"types":[{"id":"HP:0002592","label":"Gastric ulcer"}]}},{"entity":"ClinVarVariant:36794","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"ClinVarVariant:217164","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"AQTL:31966","phenotype":{"types":[{"id":"AQTLTrait:2161","label":"Femur length"}]}},{"entity":"ClinVarVariant:53219","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"ClinVarVariant:13325","phenotype":{"types":[{"id":"HP:0001644","label":"Dilated cardiomyopathy"}]}},{"entity":"ClinVarVariant:208080","phenotype":{"types":[{"id":"HP:0005478","label":"Prominent frontal sinuses"}]}},{"entity":"ClinVarVariant:42420","phenotype":{"types":[{"id":"HP:0000646","label":"Amblyopia"}]}},{"entity":"ClinVarVariant:35832","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"ClinVarVariant:36764","phenotype":{"types":[{"id":"HP:0006682","label":"Ventricular extrasystoles"}]}},{"entity":"ClinVarVariant:53493","phenotype":{"types":[{"id":"HP:0011109","label":"Chronic sinusitis"}]}},{"entity":"MGI:3590264","phenotype":{"types":[{"id":"MP:0001987","label":"alcohol preference"}]}},{"entity":"ClinVarVariant:6213","phenotype":{"types":[{"id":"HP:0003218","label":"Oroticaciduria"}]}},{"entity":"ClinVarVariant:53158","phenotype":{"types":[{"id":"HP:0004395","label":"Malnutrition"}]}},{"entity":"ClinVarVariant:188948","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00014883-WBRNAi00077884","phenotype":{"types":[{"id":"WBPhenotype:0001824","label":"meiotic progression prophase variant"}]}},{"entity":"ClinVarVariant:183330","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:41088","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:66501","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"MGI:2135666","phenotype":{"types":[{"id":"MP:0000166","label":"abnormal chondrocyte morphology"}]}},{"entity":"ClinVarVariant:2608","phenotype":{"types":[{"id":"HP:0011096","label":"Peripheral demyelination"}]}},{"entity":"ClinVarVariant:45017","phenotype":{"types":[{"id":"HP:0011663","label":"Right ventricular cardiomyopathy"}]}},{"entity":"ClinVarVariant:217252","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:6021","phenotype":{"types":[{"id":"HP:0002230","label":"Generalized hirsutism"}]}},{"entity":"ClinVarVariant:11755","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"MGI:2388715","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"MGI:4888719","phenotype":{"types":[{"id":"MP:0006060","label":"increased cerebral infarction size"}]}},{"entity":"ClinVarVariant:49751","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:162613","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:92705","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00016493-WBRNAi00096905","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"ClinVarVariant:36112","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:36577","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"FlyBase:FBal0209323","phenotype":{"types":[{"id":"FBcv:0000352","label":"partially lethal - majority die"}]}},{"entity":"ClinVarVariant:13162","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:25340","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:5509","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003084-WBRNAi00078913","phenotype":{"types":[{"id":"WBPhenotype:0000700","label":"multivulva"}]}},{"entity":"ClinVarVariant:211736","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"MGI:3775648","phenotype":{"types":[{"id":"HP:0012465","label":"Elevated hepatic iron concentration"}]}},{"entity":"ClinVarVariant:65274","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:11811","phenotype":{"types":[{"id":"HP:0000248","label":"Brachycephaly"}]}},{"entity":"ClinVarVariant:49741","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:158612","phenotype":{"types":[{"id":"HP:0007266","label":"Cerebral dysmyelination"}]}},{"entity":"MGI:2181021","phenotype":{"types":[{"id":"MP:0011086","label":"postnatal lethality, incomplete penetrance"}]}},{"entity":"MGI:4362924","phenotype":{"types":[{"id":"HP:0010976","label":"B lymphocytopenia"}]}},{"entity":"ClinVarVariant:2017","phenotype":{"types":[{"id":"HP:0000230","label":"Gingivitis"}]}},{"entity":"ClinVarVariant:2945","phenotype":{"types":[{"id":"HP:0000662","label":"Nyctalopia"}]}},{"entity":"ClinVarVariant:42325","phenotype":{"types":[{"id":"HP:0004933","label":"Ascending aortic dissection"}]}},{"entity":"WormBase:WBVar00252220","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:1451","phenotype":{"types":[{"id":"HP:0006597","label":"Diaphragmatic paralysis"}]}},{"entity":"ClinVarVariant:11082","phenotype":{"types":[{"id":"HP:0002361","label":"Psychomotor deterioration"}]}},{"entity":"ClinVarVariant:7192","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:5280","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:36102","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:2250","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"ClinVarVariant:101138","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"ClinVarVariant:10253","phenotype":{"types":[{"id":"HP:0005681","label":"Juvenile rheumatoid arthritis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00009882-WBRNAi00085534","phenotype":{"types":[{"id":"WBPhenotype:0001810","label":"oocyte septum formation variant"}]}},{"entity":"FlyBase:FBal0302452","phenotype":{"types":[{"id":"FBcv:0000316","label":"homeotic"}]}},{"entity":"ClinVarVariant:6810","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000962-WBRNAi00085605","phenotype":{"types":[{"id":"WBPhenotype:0001028","label":"nuclear appearance variant"}]}},{"entity":"ClinVarVariant:137950","phenotype":{"types":[{"id":"HP:0009765","label":"Low hanging columella"}]}},{"entity":"ClinVarVariant:53851","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:3670","phenotype":{"types":[{"id":"HP:0007957","label":"Corneal opacity"}]}},{"entity":"ClinVarVariant:143152","phenotype":{"types":[{"id":"HP:0002251","label":"Aganglionic megacolon"}]}},{"entity":"ClinVarVariant:162134","phenotype":{"types":[{"id":"HP:0007754","label":"Macular dystrophy"}]}},{"entity":"ClinVarVariant:211254","phenotype":{"types":[{"id":"HP:0001973","label":"Autoimmune thrombocytopenia"}]}},{"entity":"ClinVarVariant:167491","phenotype":{"types":[{"id":"HP:0002089","label":"Pulmonary hypoplasia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006928-WBRNAi00095274","phenotype":{"types":[{"id":"WBPhenotype:0001013","label":"pathogen susceptibility increased"}]}},{"entity":"ClinVarVariant:40678","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:42545","phenotype":{"types":[{"id":"HP:0000859","label":"Hyperaldosteronism"}]}},{"entity":"ClinVarVariant:180643","phenotype":{"types":[{"id":"HP:0002359","label":"Frequent falls"}]}},{"entity":"ClinVarVariant:65302","phenotype":{"types":[{"id":"HP:0000826","label":"Precocious puberty"}]}},{"entity":"ClinVarVariant:48947","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:4182","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:52338","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:41162","phenotype":{"types":[{"id":"HP:0003162","label":"Fasting hypoglycemia"}]}},{"entity":"MGI:2177337","phenotype":{"types":[{"id":"MP:0003934","label":"abnormal pancreas development"}]}},{"entity":"ClinVarVariant:2033","phenotype":{"types":[{"id":"HP:0000830","label":"Anterior hypopituitarism"}]}},{"entity":"ClinVarVariant:21244","phenotype":{"types":[{"id":"HP:0011362","label":"Abnormal hair quantity"}]}},{"entity":"MGI:2155977","phenotype":{"types":[{"id":"GO:0043066PHENOTYPE","label":"negative regulation of apoptotic process phenotype"}]}},{"entity":"ClinVarVariant:13903","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:184187","phenotype":{"types":[{"id":"HP:0005523","label":"Lymphoproliferative disorder"}]}},{"entity":"ClinVarVariant:126446","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:181723","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:3160","phenotype":{"types":[{"id":"HP:0001254","label":"Lethargy"}]}},{"entity":"ClinVarVariant:204097","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:10108","phenotype":{"types":[{"id":"HP:0005542","label":"Prolonged whole-blood clotting time"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000376-WBRNAi00027553","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"FlyBase:FBal0203410","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:49731","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:11736","phenotype":{"types":[{"id":"HP:0010808","label":"Protruding tongue"}]}},{"entity":"dbSNP:rs9268905","phenotype":{"types":[{"id":"HP:0002331","label":"Headache (with pheochromocytoma)"}]}},{"entity":"MGI:5548388","phenotype":{"types":[{"id":"HP:0005736","label":"Short tibia"}]}},{"entity":"WormBase:WBVar00242226","phenotype":{"types":[{"id":"WBPhenotype:0000470","label":"HSN migration variant"}]}},{"entity":"FlyBase:FBal0207110","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:41191","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:38985","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:204056","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:56302","phenotype":{"types":[{"id":"HP:0002323","label":"Anencephaly"}]}},{"entity":"ClinVarVariant:101279","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:196934","phenotype":{"types":[{"id":"HP:0002512","label":"Brain stem compression"}]}},{"entity":"MGI:2653045","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:4888","phenotype":{"types":[{"id":"HP:0100639","label":"Erectile abnormalities"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-990415-279-ZDB-MRPHLNO-070116-1","phenotype":{"types":[{"id":"GO:0021854PHENOTYPE","label":"hypothalamus development phenotype"}]}},{"entity":"ClinVarVariant:21595","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:41158","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"AQTL:15956","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:101279","phenotype":{"types":[{"id":"HP:0000015","label":"Bladder diverticulum"}]}},{"entity":"ClinVarVariant:13396","phenotype":{"types":[{"id":"HP:0007772","label":"Impaired smooth pursuit"}]}},{"entity":"ClinVarVariant:143704","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:5634328","phenotype":{"types":[{"id":"HP:0011970","label":"Cerebral amyloid angiopathy"}]}},{"entity":"AQTL:18099","phenotype":{"types":[{"id":"AQTLTrait:1153","label":"Stillbirth"}]}},{"entity":"ClinVarVariant:216145","phenotype":{"types":[{"id":"HP:0009806","label":"Nephrogenic diabetes insipidus"}]}},{"entity":"ClinVarVariant:53643","phenotype":{"types":[{"id":"HP:0100732","label":"Pancreatic fibrosis"}]}},{"entity":"ClinVarVariant:217069","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:1955","phenotype":{"types":[{"id":"HP:0001890","label":"Autoimmune hemolytic anemia"}]}},{"entity":"ClinVarVariant:39667","phenotype":{"types":[{"id":"HP:0006380","label":"Knee flexion contracture"}]}},{"entity":"AQTL:13689","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:209143","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:8762","phenotype":{"types":[{"id":"HP:0000988","label":"Skin rash"}]}},{"entity":"ZFIN:ZDB-ALT-050913-4","phenotype":{"types":[{"id":"ZP:0010859","label":"abnormal(ly) lacks parts or has fewer parts of type olfactory epithelium towards olfactory epithelium microvillous olfactory receptor neuron"}]}},{"entity":"ClinVarVariant:1221","phenotype":{"types":[{"id":"HP:0002063","label":"Rigidity"}]}},{"entity":"FlyBase:FBal0199572","phenotype":{"types":[{"id":"FBbt:00005169PHENOTYPE","label":"Drosophila trichogen cell phenotype"}]}},{"entity":"ClinVarVariant:7161","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"MGI:1931048","phenotype":{"types":[{"id":"GO:0001525PHENOTYPE","label":"angiogenesis phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001686-WBRNAi00023783","phenotype":{"types":[{"id":"WBPhenotype:0001183","label":"fat content reduced"}]}},{"entity":"ClinVarVariant:49805","phenotype":{"types":[{"id":"HP:0009720","label":"Adenoma sebaceum"}]}},{"entity":"ClinVarVariant:50874","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:53942","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"AQTL:20964","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"ClinVarVariant:183242","phenotype":{"types":[{"id":"HP:0003687","label":"Centrally nucleated skeletal muscle fibers"}]}},{"entity":"ClinVarVariant:21057","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:49848","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"MGI:4367072","phenotype":{"types":[{"id":"MP:0004753","label":"abnormal miniature excitatory postsynaptic currents"}]}},{"entity":"FlyBase:FBal0292824","phenotype":{"types":[{"id":"FBcv:0000366","label":"female sterile"}]}},{"entity":"FlyBase:FBal0130285","phenotype":{"types":[{"id":"FBcv:0000449","label":"planar polarity defective"}]}},{"entity":"ClinVarVariant:38887","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-001212-6-ZDB-MRPHLNO-060215-2","phenotype":{"types":[{"id":"ZP:0000955","label":"abnormal(ly) disrupted determination of heart left/right asymmetry"}]}},{"entity":"MGI:3528994","phenotype":{"types":[{"id":"MP:0005463","label":"abnormal CD4-positive, alpha-beta T cell physiology"}]}},{"entity":"ClinVarVariant:68698","phenotype":{"types":[{"id":"HP:0002900","label":"Hypokalemia"}]}},{"entity":"ClinVarVariant:53390","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:216707","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"ClinVarVariant:56027","phenotype":{"types":[{"id":"HP:0008434","label":"Hypoplastic cervical vertebrae"}]}},{"entity":"ClinVarVariant:126651","phenotype":{"types":[{"id":"HP:0000864","label":"Abnormality of the hypothalamus-pituitary axis"}]}},{"entity":"ClinVarVariant:82337","phenotype":{"types":[{"id":"HP:0006753","label":"Neoplasm of the stomach"}]}},{"entity":"dbSNP:rs29015207","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:4881","phenotype":{"types":[{"id":"HP:0000771","label":"Gynecomastia"}]}},{"entity":"ClinVarVariant:156326","phenotype":{"types":[{"id":"HP:0001762","label":"Talipes equinovarus"}]}},{"entity":"ClinVarVariant:3211","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007385-WBRNAi00028603","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"ClinVarVariant:92521","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"ClinVarVariant:10756","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"ClinVarVariant:11000","phenotype":{"types":[{"id":"HP:0002021","label":"Pyloric stenosis"}]}},{"entity":"MGI:3698867","phenotype":{"types":[{"id":"MP:0002047","label":"increased hepatic hemangioma incidence"}]}},{"entity":"ClinVarVariant:53648","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:53396","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:126952","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:135756","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:10194","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:204268","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:1641","phenotype":{"types":[{"id":"HP:0002942","label":"Thoracic kyphosis"}]}},{"entity":"WormBase:WBVar00089870","phenotype":{"types":[{"id":"WBPhenotype:0000425","label":"antibody staining reduced"}]}},{"entity":"ClinVarVariant:135702","phenotype":{"types":[{"id":"HP:0000684","label":"Delayed eruption of teeth"}]}},{"entity":"MGI:2137553","phenotype":{"types":[{"id":"MP:0001698","label":"decreased embryo size"}]}},{"entity":"MGI:1933761","phenotype":{"types":[{"id":"HP:0100522","label":"Thymoma"}]}},{"entity":"ClinVarVariant:135767","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:1391","phenotype":{"types":[{"id":"HP:0004639","label":"Elevated amniotic fluid alpha-fetoprotein"}]}},{"entity":"ClinVarVariant:49307","phenotype":{"types":[{"id":"HP:0009554","label":"Projection of scalp hair onto lateral cheek"}]}},{"entity":"MGI:5629408","phenotype":{"types":[{"id":"HP:0003097","label":"Short femur"}]}},{"entity":"ClinVarVariant:18334","phenotype":{"types":[{"id":"HP:0007110","label":"Central hypoventilation"}]}},{"entity":"_:genid1976156","phenotype":{"types":[{"id":"ZP:0000038","label":"abnormal(ly) edematous pericardium"}]}},{"entity":"ClinVarVariant:24775","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:9450","phenotype":{"types":[{"id":"HP:0000455","label":"Broad nasal tip"}]}},{"entity":"ClinVarVariant:204096","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:2764","phenotype":{"types":[{"id":"HP:0003019","label":"Abnormality of the wrist"}]}},{"entity":"ClinVarVariant:16814","phenotype":{"types":[{"id":"HP:0011663","label":"Right ventricular cardiomyopathy"}]}},{"entity":"ClinVarVariant:29667","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"ClinVarVariant:16303","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:181735","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:161992","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"ClinVarVariant:17272","phenotype":{"types":[{"id":"HP:0004277","label":"Fractured hand bones"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002202-WBRNAi00101493","phenotype":{"types":[{"id":"WBPhenotype:0001887","label":"excess seam cells"}]}},{"entity":"ClinVarVariant:13898","phenotype":{"types":[{"id":"HP:0001558","label":"Decreased fetal movement"}]}},{"entity":"ClinVarVariant:49526","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:24694","phenotype":{"types":[{"id":"HP:0011502","label":"Posterior lenticonus"}]}},{"entity":"FlyBase:FBal0204414","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:40983","phenotype":{"types":[{"id":"HP:0002757","label":"Recurrent fractures"}]}},{"entity":"ClinVarVariant:102723","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:14700","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:54043","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:55824","phenotype":{"types":[{"id":"HP:0001900","label":"Increased hemoglobin"}]}},{"entity":"ClinVarVariant:160314","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:159229","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:8882","phenotype":{"types":[{"id":"HP:0006989","label":"Dysplastic corpus callosum"}]}},{"entity":"ClinVarVariant:3167","phenotype":{"types":[{"id":"HP:0003419","label":"Low back pain"}]}},{"entity":"MGI:2152978","phenotype":{"types":[{"id":"HP:0008873","label":"Disproportionate short-limb short stature"}]}},{"entity":"ClinVarVariant:12975","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:127425","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:7519","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:54073","phenotype":{"types":[{"id":"HP:0006536","label":"Obstructive lung disease"}]}},{"entity":"ClinVarVariant:163768","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ZFIN:ZDB-ALT-980203-483","phenotype":{"types":[{"id":"ZP:0001317","label":"abnormal(ly) condensed pharyngeal arch cartilage"}]}},{"entity":"ClinVarVariant:192382","phenotype":{"types":[{"id":"HP:0000303","label":"Mandibular prognathia"}]}},{"entity":"ClinVarVariant:120303","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:157598","phenotype":{"types":[{"id":"HP:0001231","label":"Abnormality of the fingernails"}]}},{"entity":"MGI:3620559","phenotype":{"types":[{"id":"MP:0003719","label":"abnormal pericyte morphology"}]}},{"entity":"ClinVarVariant:216935","phenotype":{"types":[{"id":"HP:0000900","label":"Thickened ribs"}]}},{"entity":"ClinVarVariant:24548","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:143491","phenotype":{"types":[{"id":"HP:0010521","label":"Gait apraxia"}]}},{"entity":"MGI:3797077","phenotype":{"types":[{"id":"MP:0013283","label":"failure of ventral body wall closure"}]}},{"entity":"ClinVarVariant:8814","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:140832","phenotype":{"types":[{"id":"HP:0002344","label":"Progressive neurologic deterioration"}]}},{"entity":"MGI:2180365","phenotype":{"types":[{"id":"MP:0000097","label":"short maxilla"}]}},{"entity":"ClinVarVariant:56455","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:94811","phenotype":{"types":[{"id":"HP:0003713","label":"Muscle fiber necrosis"}]}},{"entity":"MGI:3579497","phenotype":{"types":[{"id":"MP:0001728","label":"failure of embryo implantation"}]}},{"entity":"ClinVarVariant:36113","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:7185","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"FlyBase:FBal0244010","phenotype":{"types":[{"id":"FBbt:00004283PHENOTYPE","label":"Drosophila prothoracic tarsal bristle phenotype"}]}},{"entity":"ClinVarVariant:101145","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:7444","phenotype":{"types":[{"id":"HP:0000771","label":"Gynecomastia"}]}},{"entity":"MGI:4457504","phenotype":{"types":[{"id":"HP:0003076","label":"Glycosuria"}]}},{"entity":"ClinVarVariant:50854","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"MGI:2449290","phenotype":{"types":[{"id":"HP:0100738","label":"Abnormal eating behavior"}]}},{"entity":"ClinVarVariant:5859","phenotype":{"types":[{"id":"HP:0000684","label":"Delayed eruption of teeth"}]}},{"entity":"ClinVarVariant:41151","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:1985","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:66441","phenotype":{"types":[{"id":"HP:0100707","label":"Abnormality of the astrocytes"}]}},{"entity":"MGI:2386172","phenotype":{"types":[{"id":"MP:0002118","label":"abnormal lipid homeostasis"}]}},{"entity":"ClinVarVariant:53972","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:42363","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"MGI:2150350","phenotype":{"types":[{"id":"HP:0001669","label":"Transposition of the great arteries"}]}},{"entity":"ClinVarVariant:127150","phenotype":{"types":[{"id":"HP:0001321","label":"Cerebellar hypoplasia"}]}},{"entity":"MGI:1855936","phenotype":{"types":[{"id":"HP:0009887","label":"Abnormality of hair pigmentation"}]}},{"entity":"_:genid1972365","phenotype":{"types":[{"id":"ZP:0014893","label":"abnormal(ly) process quality response to gamma radiation"}]}},{"entity":"ClinVarVariant:30547","phenotype":{"types":[{"id":"HP:0000972","label":"Palmoplantar hyperkeratosis"}]}},{"entity":"ClinVarVariant:53788","phenotype":{"types":[{"id":"HP:0100646","label":"Thyroiditis"}]}},{"entity":"MGI:3041864","phenotype":{"types":[{"id":"MP:0008395","label":"abnormal osteoblast differentiation"}]}},{"entity":"MGI:1856910","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:142043","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:216224","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:210843","phenotype":{"types":[{"id":"HP:0100495","label":"Mastocytosis"}]}},{"entity":"ClinVarVariant:25184","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:143181","phenotype":{"types":[{"id":"HP:0001123","label":"Visual field defect"}]}},{"entity":"FlyBase:FBal0198615","phenotype":{"types":[{"id":"FBcv:0000386","label":"long lived"}]}},{"entity":"ClinVarVariant:189163","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:41364","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:7945","phenotype":{"types":[{"id":"HP:0000077","label":"Abnormality of the kidney"}]}},{"entity":"MGI:3051523","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"FlyBase:FBal0213272","phenotype":{"types":[{"id":"FBcv:0000356","label":"body color defective"}]}},{"entity":"ClinVarVariant:9143","phenotype":{"types":[{"id":"HP:0003455","label":"Elevated long chain fatty acids"}]}},{"entity":"ClinVarVariant:35823","phenotype":{"types":[{"id":"HP:0001742","label":"Nasal obstruction"}]}},{"entity":"ClinVarVariant:10460","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:101300","phenotype":{"types":[{"id":"HP:0100784","label":"Peripheral arteriovenous fistula"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022281-WBRNAi00098373","phenotype":{"types":[{"id":"WBPhenotype:0001566","label":"ventral enclosure variant"}]}},{"entity":"AQTL:28586","phenotype":{"types":[{"id":"AQTLTrait:1169","label":"Interval to first estrus after calving"}]}},{"entity":"dbSNP:rs43697015","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:10723","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"AQTL:13101","phenotype":{"types":[{"id":"AQTLTrait:1110","label":"Muscle protein percentage"}]}},{"entity":"ClinVarVariant:53234","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:17380","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:133325","phenotype":{"types":[{"id":"HP:0002317","label":"Unsteady gait"}]}},{"entity":"ClinVarVariant:93761","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"MGI:5320677","phenotype":{"types":[{"id":"HP:0001899","label":"Increased hematocrit"}]}},{"entity":"ClinVarVariant:159128","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:49173","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:36035","phenotype":{"types":[{"id":"HP:0000541","label":"Retinal detachment"}]}},{"entity":"ClinVarVariant:209052","phenotype":{"types":[{"id":"HP:0002107","label":"Pneumothorax"}]}},{"entity":"ClinVarVariant:204278","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:13560","phenotype":{"types":[{"id":"HP:0001873","label":"Thrombocytopenia"}]}},{"entity":"ClinVarVariant:2456","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"MGI:5548068","phenotype":{"types":[{"id":"MP:0001265","label":"decreased body size"}]}},{"entity":"ClinVarVariant:834","phenotype":{"types":[{"id":"HP:0006000","label":"Ureteral obstruction"}]}},{"entity":"ClinVarVariant:1676","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"FlyBase:FBal0125280","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"dbSNP:rs41628993","phenotype":{"types":[{"id":"AQTLTrait:1067","label":"Length of productive life"}]}},{"entity":"ClinVarVariant:3445","phenotype":{"types":[{"id":"HP:0000085","label":"Horseshoe kidney"}]}},{"entity":"ClinVarVariant:101410","phenotype":{"types":[{"id":"HP:0000790","label":"Hematuria"}]}},{"entity":"ClinVarVariant:53404","phenotype":{"types":[{"id":"HP:0100512","label":"Vitamin D deficiency"}]}},{"entity":"ClinVarVariant:197210","phenotype":{"types":[{"id":"HP:0008261","label":"Pancreatic islet cell adenoma"}]}},{"entity":"MGI:2387852","phenotype":{"types":[{"id":"GO:0070192PHENOTYPE","label":"chromosome organization involved in meiosis phenotype"}]}},{"entity":"FlyBase:FBal0044814","phenotype":{"types":[{"id":"FBbt:00003479PHENOTYPE","label":"Drosophila abdominal ventral muscle phenotype"}]}},{"entity":"ClinVarVariant:177938","phenotype":{"types":[{"id":"HP:0100749","label":"Chest pain"}]}},{"entity":"ClinVarVariant:2139","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ClinVarVariant:24395","phenotype":{"types":[{"id":"HP:0000093","label":"Proteinuria"}]}},{"entity":"MGI:3696958","phenotype":{"types":[{"id":"HP:0100678","label":"Premature skin wrinkling"}]}},{"entity":"ClinVarVariant:36123","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:156339","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:67976","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:157934","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"ClinVarVariant:5408","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:30450","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000209-WBRNAi00073191","phenotype":{"types":[{"id":"WBPhenotype:0001037","label":"sterile progeny"}]}},{"entity":"ClinVarVariant:8814","phenotype":{"types":[{"id":"HP:0004964","label":"Pulmonary arterial medial hypertrophy"}]}},{"entity":"ClinVarVariant:6465","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"MGI:3047647","phenotype":{"types":[{"id":"GO:0043249PHENOTYPE","label":"erythrocyte maturation phenotype"}]}},{"entity":"FlyBase:FBal0204879","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:17309","phenotype":{"types":[{"id":"HP:0007759","label":"Opacification of the corneal stroma"}]}},{"entity":"ClinVarVariant:9368","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:126748","phenotype":{"types":[{"id":"HP:0100760","label":"Clubbing of toes"}]}},{"entity":"ClinVarVariant:161993","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"MGI:2156498","phenotype":{"types":[{"id":"MP:0011086","label":"postnatal lethality, incomplete penetrance"}]}},{"entity":"ClinVarVariant:428","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:53316","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:67838","phenotype":{"types":[{"id":"HP:0004756","label":"Ventricular tachycardia"}]}},{"entity":"ClinVarVariant:211468","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:158542","phenotype":{"types":[{"id":"HP:0010719","label":"Abnormality of hair texture"}]}},{"entity":"ClinVarVariant:158830","phenotype":{"types":[{"id":"HP:0008678","label":"Renal hypoplasia/aplasia"}]}},{"entity":"MGI:1858030","phenotype":{"types":[{"id":"MP:0000819","label":"abnormal olfactory bulb morphology"}]}},{"entity":"MGI:4421413","phenotype":{"types":[{"id":"HP:0011373","label":"Incomplete partition of the cochlea"}]}},{"entity":"ClinVarVariant:25287","phenotype":{"types":[{"id":"HP:0008209","label":"Premature ovarian failure"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004306-WBRNAi00027441","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:161401","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"ClinVarVariant:12010","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"ClinVarVariant:49791","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:49215","phenotype":{"types":[{"id":"HP:0009719","label":"Hypomelanotic macule"}]}},{"entity":"ClinVarVariant:94759","phenotype":{"types":[{"id":"HP:0001644","label":"Dilated cardiomyopathy"}]}},{"entity":"ClinVarVariant:4531","phenotype":{"types":[{"id":"HP:0000144","label":"Decreased fertility"}]}},{"entity":"ClinVarVariant:37353","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:97583","phenotype":{"types":[{"id":"HP:0005214","label":"Intestinal obstruction"}]}},{"entity":"ClinVarVariant:194555","phenotype":{"types":[{"id":"HP:0200134","label":"Epileptic encephalopathy"}]}},{"entity":"FlyBase:FBal0208599","phenotype":{"types":[{"id":"FBcv:0000393","label":"pain response defective"}]}},{"entity":"MGI:5295237","phenotype":{"types":[{"id":"MP:0008498","label":"decreased IgG3 level"}]}},{"entity":"ClinVarVariant:10606","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"MGI:3043578","phenotype":{"types":[{"id":"MP:0001382","label":"abnormal nursing"}]}},{"entity":"ClinVarVariant:10251","phenotype":{"types":[{"id":"HP:0100773","label":"Cartilage destruction"}]}},{"entity":"ClinVarVariant:97709","phenotype":{"types":[{"id":"HP:0001677","label":"Coronary artery disease"}]}},{"entity":"ClinVarVariant:53959","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ClinVarVariant:54093","phenotype":{"types":[{"id":"HP:0000966","label":"Hypohidrosis"}]}},{"entity":"ClinVarVariant:64918","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:4348","phenotype":{"types":[{"id":"HP:0002839","label":"Urinary bladder sphincter dysfunction"}]}},{"entity":"MGI:3610995","phenotype":{"types":[{"id":"MP:0002910","label":"abnormal excitatory postsynaptic currents"}]}},{"entity":"AQTL:55082","phenotype":{"types":[{"id":"AQTLTrait:1153","label":"Stillbirth"}]}},{"entity":"ClinVarVariant:4380","phenotype":{"types":[{"id":"HP:0001281","label":"Tetany"}]}},{"entity":"ClinVarVariant:198424","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"ClinVarVariant:188978","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:6029","phenotype":{"types":[{"id":"HP:0003693","label":"Distal amyotrophy"}]}},{"entity":"ClinVarVariant:5243","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:11483","phenotype":{"types":[{"id":"HP:0003462","label":"Elevated 8-dehydrocholesterol"}]}},{"entity":"ClinVarVariant:49772","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:41177","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"MGI:1857718","phenotype":{"types":[{"id":"MP:0003691","label":"abnormal microglial cell physiology"}]}},{"entity":"ClinVarVariant:158369","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:217105","phenotype":{"types":[{"id":"HP:0001012","label":"Multiple lipomas"}]}},{"entity":"ClinVarVariant:55823","phenotype":{"types":[{"id":"HP:0000864","label":"Abnormality of the hypothalamus-pituitary axis"}]}},{"entity":"ClinVarVariant:14364","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"ClinVarVariant:127699","phenotype":{"types":[{"id":"HP:0002576","label":"Intussusception"}]}},{"entity":"ClinVarVariant:66051","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:4868762","phenotype":{"types":[{"id":"MP:0000428","label":"abnormal craniofacial morphology"}]}},{"entity":"ClinVarVariant:4305","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"MGI:3717494","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"WormBase:WBVar00142947","phenotype":{"types":[{"id":"WBPhenotype:0000644","label":"paralyzed"}]}},{"entity":"dbSNP:rs1896295","phenotype":{"types":[{"id":"HP:0002754","label":"Osteomyelitis"}]}},{"entity":"ClinVarVariant:65505","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:333","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:11675","phenotype":{"types":[{"id":"HP:0000233","label":"Thin vermilion border"}]}},{"entity":"ClinVarVariant:204117","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:8804","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:64705","phenotype":{"types":[{"id":"HP:0009716","label":"Subependymal nodules"}]}},{"entity":"dbSNP:rs1427407","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"FlyBase:FBal0285746","phenotype":{"types":[{"id":"FBbt:00005201PHENOTYPE","label":"denticle belt phenotype"}]}},{"entity":"ClinVarVariant:217428","phenotype":{"types":[{"id":"HP:0001231","label":"Abnormality of the fingernails"}]}},{"entity":"ClinVarVariant:95624","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ZFIN:ZDB-ALT-020426-56","phenotype":{"types":[{"id":"GO:0060036PHENOTYPE","label":"notochord cell vacuolation phenotype"}]}},{"entity":"dbSNP:rs11986414","phenotype":{"types":[{"id":"HP:0002756","label":"Pathologic fracture"}]}},{"entity":"ClinVarVariant:188893","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"ClinVarVariant:7404","phenotype":{"types":[{"id":"HP:0002226","label":"White eyebrow"}]}},{"entity":"ClinVarVariant:25390","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"dbSNP:rs3105491","phenotype":{"types":[{"id":"HP:0004825","label":"Increased hemoglobin oxygen affinity"}]}},{"entity":"ClinVarVariant:204086","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:49792","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:136076","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003992-WBRNAi00084326","phenotype":{"types":[{"id":"WBPhenotype:0000061","label":"extended life span"}]}},{"entity":"ClinVarVariant:38917","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:8137","phenotype":{"types":[{"id":"HP:0001002","label":"Decreased subcutaneous fat"}]}},{"entity":"ClinVarVariant:16085","phenotype":{"types":[{"id":"HP:0000055","label":"Abnormality of female external genitalia"}]}},{"entity":"ClinVarVariant:11362","phenotype":{"types":[{"id":"HP:0200042","label":"Skin ulcer"}]}},{"entity":"ClinVarVariant:101206","phenotype":{"types":[{"id":"HP:0000023","label":"Inguinal hernia"}]}},{"entity":"ClinVarVariant:53224","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:39727","phenotype":{"types":[{"id":"HP:0002239","label":"Gastrointestinal hemorrhage"}]}},{"entity":"ClinVarVariant:21106","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:91405","phenotype":{"types":[{"id":"HP:0002472","label":"Small cerebral cortex"}]}},{"entity":"FlyBase:FBal0144279","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011897-WBRNAi00095734","phenotype":{"types":[{"id":"WBPhenotype:0000402","label":"avoids bacterial lawn"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008149-WBRNAi00029911","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"ClinVarVariant:161364","phenotype":{"types":[{"id":"HP:0002486","label":"Myotonia"}]}},{"entity":"ClinVarVariant:2249","phenotype":{"types":[{"id":"HP:0001287","label":"Meningitis"}]}},{"entity":"FlyBase:FBal0270164","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:56689","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:102786","phenotype":{"types":[{"id":"HP:0005599","label":"Hypopigmentation of hair"}]}},{"entity":"ClinVarVariant:25221","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"AQTL:39589","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"dbSNP:rs10005603","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:35514","phenotype":{"types":[{"id":"HP:0000622","label":"Blurred vision"}]}},{"entity":"ClinVarVariant:179339","phenotype":{"types":[{"id":"HP:0001696","label":"Situs inversus totalis"}]}},{"entity":"ClinVarVariant:52328","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"dbSNP:rs6545883","phenotype":{"types":[{"id":"HP:0008207","label":"Primary adrenal insufficiency"}]}},{"entity":"AQTL:16175","phenotype":{"types":[{"id":"AQTLTrait:1044","label":"Milk yield"}]}},{"entity":"WormBase:WBVar00242144","phenotype":{"types":[{"id":"WBPhenotype:0000116","label":"mid larval lethal"}]}},{"entity":"ClinVarVariant:53973","phenotype":{"types":[{"id":"HP:0100582","label":"Nasal polyposis"}]}},{"entity":"ClinVarVariant:10872","phenotype":{"types":[{"id":"HP:0000286","label":"Epicanthus"}]}},{"entity":"ClinVarVariant:159191","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"ClinVarVariant:210786","phenotype":{"types":[{"id":"HP:0005306","label":"Capillary hemangiomas"}]}},{"entity":"ClinVarVariant:133075","phenotype":{"types":[{"id":"HP:0003738","label":"Exercise-induced myalgia"}]}},{"entity":"ClinVarVariant:211503","phenotype":{"types":[{"id":"HP:0000171","label":"Microglossia"}]}},{"entity":"ClinVarVariant:21274","phenotype":{"types":[{"id":"HP:0002827","label":"Hip dislocation"}]}},{"entity":"ClinVarVariant:14662","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:189027","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"MGI:3777553","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:16869","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ZFIN:ZDB-ALT-090625-1","phenotype":{"types":[{"id":"ZP:0004126","label":"abnormal(ly) absent intrahepatic bile duct"}]}},{"entity":"ClinVarVariant:35575","phenotype":{"types":[{"id":"HP:0001061","label":"Acne"}]}},{"entity":"ClinVarVariant:41181","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:7435","phenotype":{"types":[{"id":"HP:0000581","label":"Blepharophimosis"}]}},{"entity":"ClinVarVariant:56414","phenotype":{"types":[{"id":"HP:0003452","label":"Increased serum iron"}]}},{"entity":"ClinVarVariant:11159","phenotype":{"types":[{"id":"HP:0011948","label":"Acute respiratory tract infection"}]}},{"entity":"MGI:5311612","phenotype":{"types":[{"id":"MP:0002080","label":"prenatal lethality"}]}},{"entity":"ClinVarVariant:5116","phenotype":{"types":[{"id":"HP:0002857","label":"Genu valgum"}]}},{"entity":"ClinVarVariant:198034","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"FlyBase:FBal0244011","phenotype":{"types":[{"id":"FBbt:00004233PHENOTYPE","label":"Drosophila tertiary pigment cell phenotype"}]}},{"entity":"ClinVarVariant:97913","phenotype":{"types":[{"id":"HP:0001917","label":"Renal amyloidosis"}]}},{"entity":"ClinVarVariant:159983","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"ClinVarVariant:157955","phenotype":{"types":[{"id":"HP:0100022","label":"Abnormality of movement"}]}},{"entity":"ClinVarVariant:38312","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:158564","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"MGI:2674291","phenotype":{"types":[{"id":"MP:0000031","label":"abnormal cochlea morphology"}]}},{"entity":"ClinVarVariant:7230","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"NCBIGene:7467","phenotype":{"types":[{"id":"HP:0009778","label":"Short thumb"}]}},{"entity":"ClinVarVariant:56562","phenotype":{"types":[{"id":"HP:0000457","label":"Depressed nasal ridge"}]}},{"entity":"ClinVarVariant:155828","phenotype":{"types":[{"id":"HP:0000189","label":"Narrow palate"}]}},{"entity":"ClinVarVariant:182975","phenotype":{"types":[{"id":"HP:0002666","label":"Pheochromocytoma"}]}},{"entity":"FlyBase:FBal0206553","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:53925","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"NCBIGene:140906","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"FlyBase:FBal0159762","phenotype":{"types":[{"id":"FBbt:00005838PHENOTYPE","label":"NMJ bouton phenotype"}]}},{"entity":"ClinVarVariant:96117","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:14347","phenotype":{"types":[{"id":"HP:0002013","label":"Vomiting"}]}},{"entity":"ClinVarVariant:41334","phenotype":{"types":[{"id":"HP:0007067","label":"Distal peripheral sensory neuropathy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019801-WBRNAi00082236","phenotype":{"types":[{"id":"WBPhenotype:0001541","label":"dauer gonad arrest variant"}]}},{"entity":"ClinVarVariant:49738","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"MGI:2388352","phenotype":{"types":[{"id":"MP:0001274","label":"curly vibrissae"}]}},{"entity":"MGI:3690317","phenotype":{"types":[{"id":"HP:0012184","label":"Hyperalphalipoproteinemia"}]}},{"entity":"ClinVarVariant:159478","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"ClinVarVariant:4296","phenotype":{"types":[{"id":"HP:0011857","label":"Plasmacytoma"}]}},{"entity":"ClinVarVariant:53697","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019268-WBRNAi00008936","phenotype":{"types":[{"id":"WBPhenotype:0000032","label":"sick"}]}},{"entity":"ClinVarVariant:181743","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:1381","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"MGI:5520177","phenotype":{"types":[{"id":"HP:0000752","label":"Hyperactivity"}]}},{"entity":"FlyBase:FBal0208692","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:4613","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"MGI:1857196","phenotype":{"types":[{"id":"MP:0006082","label":"CNS inflammation"}]}},{"entity":"ClinVarVariant:216024","phenotype":{"types":[{"id":"HP:0002073","label":"Progressive cerebellar ataxia"}]}},{"entity":"ClinVarVariant:101299","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:36103","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:36315","phenotype":{"types":[{"id":"HP:0001025","label":"Urticaria"}]}},{"entity":"ClinVarVariant:181495","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:11362","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"FlyBase:FBal0147448","phenotype":{"types":[{"id":"FBcv:0000414","label":"locomotor behavior defective"}]}},{"entity":"ClinVarVariant:180350","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:1185","phenotype":{"types":[{"id":"HP:0000013","label":"Hypoplasia of the uterus"}]}},{"entity":"FlyBase:FBal0305239","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"dbSNP:rs41648982","phenotype":{"types":[{"id":"AQTLTrait:1120","label":"Thurl width"}]}},{"entity":"ClinVarVariant:159128","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"ClinVarVariant:6097","phenotype":{"types":[{"id":"HP:0006315","label":"Single median maxillary incisor"}]}},{"entity":"ClinVarVariant:10219","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:188945","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:101148","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00014088-WBRNAi00027107","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:53370","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:38995","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"dbSNP:rs109034504","phenotype":{"types":[{"id":"AQTLTrait:1070","label":"Inseminations per conception"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003026-WBRNAi00085490","phenotype":{"types":[{"id":"WBPhenotype:0001973","label":"germ cell compartment size variant"}]}},{"entity":"ClinVarVariant:18346","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:6094","phenotype":{"types":[{"id":"HP:0000748","label":"Inappropriate laughter"}]}},{"entity":"ClinVarVariant:56708","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"FlyBase:FBal0181584","phenotype":{"types":[{"id":"FBcv:0000450","label":"developmental rate defective"}]}},{"entity":"ClinVarVariant:159663","phenotype":{"types":[{"id":"HP:0006461","label":"Proximal femoral epiphysiolysis"}]}},{"entity":"MGI:104735","phenotype":{"types":[{"id":"MP:0002169","label":"no abnormal phenotype detected"}]}},{"entity":"ClinVarVariant:30538","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:17168","phenotype":{"types":[{"id":"HP:0006149","label":"Increased laxity of fingers"}]}},{"entity":"FlyBase:FBal0058344","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:21208","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:29973","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:2618","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:68708","phenotype":{"types":[{"id":"HP:0002900","label":"Hypokalemia"}]}},{"entity":"MGI:3620798","phenotype":{"types":[{"id":"MP:0002410","label":"decreased susceptibility to viral infection"}]}},{"entity":"MGI:3774341","phenotype":{"types":[{"id":"MP:0003203","label":"increased neuron apoptosis"}]}},{"entity":"ClinVarVariant:6552","phenotype":{"types":[{"id":"HP:0002213","label":"Fine hair"}]}},{"entity":"ClinVarVariant:56706","phenotype":{"types":[{"id":"HP:0002074","label":"Increased neuronal autofluorescent lipopigment"}]}},{"entity":"ClinVarVariant:40494","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"ClinVarVariant:10299","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:3050446","phenotype":{"types":[{"id":"MP:0004564","label":"enlarged myocardial fiber"}]}},{"entity":"ClinVarVariant:209062","phenotype":{"types":[{"id":"HP:0002107","label":"Pneumothorax"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001031-WBRNAi00072843","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:53980","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"ClinVarVariant:36058","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"AQTL:16912","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:211716","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:9319","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:30750","phenotype":{"types":[{"id":"HP:0003228","label":"Hypernatremia"}]}},{"entity":"ClinVarVariant:188958","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:211640","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:35842","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"ClinVarVariant:162384","phenotype":{"types":[{"id":"HP:0008070","label":"Sparse hair"}]}},{"entity":"MGI:5430994","phenotype":{"types":[{"id":"HP:0005576","label":"Tubulointerstitial fibrosis"}]}},{"entity":"ClinVarVariant:5645","phenotype":{"types":[{"id":"HP:0030507","label":"Retinal crystals"}]}},{"entity":"ClinVarVariant:40164","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00077457-WBRNAi00063328","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:14209","phenotype":{"types":[{"id":"HP:0000960","label":"Sacral dimple"}]}},{"entity":"ClinVarVariant:14097","phenotype":{"types":[{"id":"HP:0001712","label":"Left ventricular hypertrophy"}]}},{"entity":"ClinVarVariant:198504","phenotype":{"types":[{"id":"HP:0008443","label":"Spinal deformities"}]}},{"entity":"MGI:3695137","phenotype":{"types":[{"id":"MP:0005463","label":"abnormal CD4-positive, alpha-beta T cell physiology"}]}},{"entity":"ClinVarVariant:6067","phenotype":{"types":[{"id":"HP:0200055","label":"Small hand"}]}},{"entity":"ClinVarVariant:2669","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:97554","phenotype":{"types":[{"id":"HP:0000999","label":"Pyoderma"}]}},{"entity":"ClinVarVariant:24752","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:67777","phenotype":{"types":[{"id":"HP:0001696","label":"Situs inversus totalis"}]}},{"entity":"ClinVarVariant:6820","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"AQTL:41673","phenotype":{"types":[{"id":"AQTLTrait:1136","label":"Bone quality"}]}},{"entity":"ClinVarVariant:14209","phenotype":{"types":[{"id":"HP:0001875","label":"Neutropenia"}]}},{"entity":"ClinVarVariant:36946","phenotype":{"types":[{"id":"HP:0001915","label":"Aplastic anemia"}]}},{"entity":"ClinVarVariant:210456","phenotype":{"types":[{"id":"HP:0003819","label":"Death in childhood"}]}},{"entity":"ClinVarVariant:30945","phenotype":{"types":[{"id":"HP:0000388","label":"Otitis media"}]}},{"entity":"ClinVarVariant:49452","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:181763","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:6625","phenotype":{"types":[{"id":"HP:0000998","label":"Hypertrichosis"}]}},{"entity":"ClinVarVariant:83156","phenotype":{"types":[{"id":"HP:0006740","label":"Transitional cell carcinoma of the bladder"}]}},{"entity":"ClinVarVariant:36913","phenotype":{"types":[{"id":"HP:0002664","label":"Neoplasm"}]}},{"entity":"ClinVarVariant:42284","phenotype":{"types":[{"id":"HP:0004935","label":"Pulmonary artery atresia"}]}},{"entity":"MGI:1888408","phenotype":{"types":[{"id":"MP:0005641","label":"increased mean corpuscular hemoglobin concentration"}]}},{"entity":"ClinVarVariant:17696","phenotype":{"types":[{"id":"HP:0004370","label":"Abnormality of temperature regulation"}]}},{"entity":"ClinVarVariant:211746","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:25350","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:53346","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:13346","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"FlyBase:FBal0205447","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:65275","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"ClinVarVariant:53784","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:16623","phenotype":{"types":[{"id":"HP:0001371","label":"Flexion contracture"}]}},{"entity":"ClinVarVariant:48902","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"ClinVarVariant:189811","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:53373","phenotype":{"types":[{"id":"HP:0006706","label":"Cystic liver disease"}]}},{"entity":"ClinVarVariant:53337","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"MGI:4868451","phenotype":{"types":[{"id":"GO:0021697PHENOTYPE","label":"cerebellar cortex formation phenotype"}]}},{"entity":"AQTL:27090","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:92715","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:91403","phenotype":{"types":[{"id":"HP:0008678","label":"Renal hypoplasia/aplasia"}]}},{"entity":"ClinVarVariant:42015","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:68718","phenotype":{"types":[{"id":"HP:0002900","label":"Hypokalemia"}]}},{"entity":"ClinVarVariant:136097","phenotype":{"types":[{"id":"HP:0001166","label":"Arachnodactyly"}]}},{"entity":"ClinVarVariant:93448","phenotype":{"types":[{"id":"HP:0003271","label":"Visceromegaly"}]}},{"entity":"ClinVarVariant:10158","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"ClinVarVariant:188958","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"FlyBase:FBal0093398","phenotype":{"types":[{"id":"FBbt:00007115PHENOTYPE","label":"embryonic/larval neuroblast phenotype"}]}},{"entity":"ClinVarVariant:6066","phenotype":{"types":[{"id":"HP:0011318","label":"Bicoronal synostosis"}]}},{"entity":"ClinVarVariant:12534","phenotype":{"types":[{"id":"HP:0004493","label":"Craniofacial hyperostosis"}]}},{"entity":"ClinVarVariant:25214","phenotype":{"types":[{"id":"HP:0010741","label":"Edema of the lower limbs"}]}},{"entity":"FlyBase:FBal0263650","phenotype":{"types":[{"id":"FBbt:00004193PHENOTYPE","label":"cone cell phenotype"}]}},{"entity":"ClinVarVariant:53702","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"ClinVarVariant:2691","phenotype":{"types":[{"id":"HP:0011073","label":"Abnormality of dental color"}]}},{"entity":"ClinVarVariant:2143","phenotype":{"types":[{"id":"HP:0003083","label":"Dislocated radial head"}]}},{"entity":"ClinVarVariant:54083","phenotype":{"types":[{"id":"HP:0004401","label":"Meconium ileus"}]}},{"entity":"ClinVarVariant:35862","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"ClinVarVariant:158299","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:11515","phenotype":{"types":[{"id":"HP:0004594","label":"Hump-shaped mound of bone in central and posterior portions of vertebral endplate"}]}},{"entity":"ClinVarVariant:189750","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:16425","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"ClinVarVariant:60494","phenotype":{"types":[{"id":"HP:0002652","label":"Skeletal dysplasia"}]}},{"entity":"ClinVarVariant:216824","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:12281","phenotype":{"types":[{"id":"HP:0002908","label":"Conjugated hyperbilirubinemia"}]}},{"entity":"AQTL:46013","phenotype":{"types":[{"id":"AQTLTrait:1115","label":"Chest width"}]}},{"entity":"ClinVarVariant:135760","phenotype":{"types":[{"id":"HP:0012189","label":"Hodgkin lymphoma"}]}},{"entity":"MGI:5510759","phenotype":{"types":[{"id":"MP:0004794","label":"increased anti-nuclear antigen antibody level"}]}},{"entity":"MGI:2679886","phenotype":{"types":[{"id":"HP:0002011","label":"Morphological abnormality of the central nervous system"}]}},{"entity":"MGI:1857437","phenotype":{"types":[{"id":"MP:0003477","label":"abnormal nerve fiber response"}]}},{"entity":"MGI:1931041","phenotype":{"types":[{"id":"MP:0013164","label":"abnormal forelimb bud morphology"}]}},{"entity":"ClinVarVariant:56445","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:21512","phenotype":{"types":[{"id":"HP:0003233","label":"Hypoalphalipoproteinemia"}]}},{"entity":"ClinVarVariant:50091","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:2149","phenotype":{"types":[{"id":"HP:0000089","label":"Renal hypoplasia"}]}},{"entity":"ClinVarVariant:143395","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:30199","phenotype":{"types":[{"id":"HP:0001220","label":"Interphalangeal joint contracture of finger"}]}},{"entity":"ClinVarVariant:12524","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:36101","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:139581","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"ClinVarVariant:211726","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"FlyBase:FBal0150725","phenotype":{"types":[{"id":"FBbt:00003361PHENOTYPE","label":"indirect flight muscle phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019218-WBRNAi00086983","phenotype":{"types":[{"id":"WBPhenotype:0000038","label":"exploded through vulva"}]}},{"entity":"ClinVarVariant:216978","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"FlyBase:FBal0189919","phenotype":{"types":[{"id":"FBcv:0000356","label":"body color defective"}]}},{"entity":"ClinVarVariant:12048","phenotype":{"types":[{"id":"HP:0004947","label":"Arteriovenous fistula"}]}},{"entity":"ClinVarVariant:25350","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:5983","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:9521","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:5198","phenotype":{"types":[{"id":"HP:0100261","label":"Abnormal tendon morphology"}]}},{"entity":"ClinVarVariant:179126","phenotype":{"types":[{"id":"HP:0003805","label":"Rimmed vacuoles"}]}},{"entity":"MGI:1857150","phenotype":{"types":[{"id":"MP:0006413","label":"increased T cell apoptosis"}]}},{"entity":"MGI:3833397","phenotype":{"types":[{"id":"HP:0100763","label":"Abnormality of the lymphatic system"}]}},{"entity":"ClinVarVariant:3364","phenotype":{"types":[{"id":"HP:0200040","label":"Epidermoid cyst"}]}},{"entity":"MGI:3613611","phenotype":{"types":[{"id":"MP:0002836","label":"abnormal chorion morphology"}]}},{"entity":"ClinVarVariant:50874","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"FlyBase:FBal0283530","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"AQTL:50857","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"dbSNP:rs12386026","phenotype":{"types":[{"id":"HP:0001510","label":"Growth delay"}]}},{"entity":"ClinVarVariant:30725","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:11422","phenotype":{"types":[{"id":"HP:0011003","label":"Severe Myopia"}]}},{"entity":"ClinVarVariant:2915","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1443","phenotype":{"types":[{"id":"ZP:0001246","label":"abnormal(ly) morphology inner ear"}]}},{"entity":"MGI:2387973","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:53725","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"MGI:2386460","phenotype":{"types":[{"id":"MP:0000880","label":"decreased Purkinje cell number"}]}},{"entity":"ClinVarVariant:189842","phenotype":{"types":[{"id":"HP:0002384","label":"Focal seizures with impairment of consciousness or awareness"}]}},{"entity":"ClinVarVariant:162019","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:9590","phenotype":{"types":[{"id":"HP:0000762","label":"Decreased nerve conduction velocity"}]}},{"entity":"ClinVarVariant:53660","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"MGI:3628446","phenotype":{"types":[{"id":"MP:0004379","label":"wide frontal bone"}]}},{"entity":"ClinVarVariant:16330","phenotype":{"types":[{"id":"HP:0000256","label":"Macrocephaly"}]}},{"entity":"ClinVarVariant:2577","phenotype":{"types":[{"id":"HP:0000660","label":"Lipemia retinalis"}]}},{"entity":"ClinVarVariant:157514","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"ClinVarVariant:2627","phenotype":{"types":[{"id":"HP:0010743","label":"Short metatarsal"}]}},{"entity":"ClinVarVariant:10194","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:88859","phenotype":{"types":[{"id":"HP:0000091","label":"Abnormality of the renal tubule"}]}},{"entity":"ClinVarVariant:56718","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"ClinVarVariant:53254","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:3792","phenotype":{"types":[{"id":"HP:0001022","label":"Albinism"}]}},{"entity":"ClinVarVariant:53912","phenotype":{"types":[{"id":"HP:0001082","label":"Cholecystitis"}]}},{"entity":"ClinVarVariant:42566","phenotype":{"types":[{"id":"HP:0001297","label":"Stroke"}]}},{"entity":"ClinVarVariant:10669","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:6895","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"ClinVarVariant:12414","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"WormBase:WBVar01473710","phenotype":{"types":[{"id":"WBPhenotype:0000643","label":"locomotion variant"}]}},{"entity":"ClinVarVariant:182828","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:7984","phenotype":{"types":[{"id":"HP:0003189","label":"Long nose"}]}},{"entity":"ClinVarVariant:186330","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"MGI:3702746","phenotype":{"types":[{"id":"HP:0012087","label":"Abnormal mitochondrial shape"}]}},{"entity":"ClinVarVariant:216684","phenotype":{"types":[{"id":"HP:0000020","label":"Urinary incontinence"}]}},{"entity":"ClinVarVariant:65134","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:65092","phenotype":{"types":[{"id":"HP:0009719","label":"Hypomelanotic macule"}]}},{"entity":"ClinVarVariant:101385","phenotype":{"types":[{"id":"HP:0005293","label":"Venous insufficiency"}]}},{"entity":"ClinVarVariant:159912","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:181753","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"WormBase:WBVar00240990","phenotype":{"types":[{"id":"MP:0002209","label":"decreased germ cell number"}]}},{"entity":"ClinVarVariant:21729","phenotype":{"types":[{"id":"HP:0001080","label":"Biliary tract abnormality"}]}},{"entity":"ClinVarVariant:180360","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:53458","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"ClinVarVariant:6668","phenotype":{"types":[{"id":"HP:0009025","label":"Increased connective tissue"}]}},{"entity":"ClinVarVariant:2086","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"AQTL:12518","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"ClinVarVariant:54185","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:3965","phenotype":{"types":[{"id":"HP:0007633","label":"Bilateral microphthalmos"}]}},{"entity":"AQTL:26646","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:210770","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:166724","phenotype":{"types":[{"id":"HP:0003774","label":"Stage 5 chronic kidney disease"}]}},{"entity":"ClinVarVariant:143294","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"ClinVarVariant:36126","phenotype":{"types":[{"id":"HP:0008132","label":"Medial rotation of the medial malleolus"}]}},{"entity":"ClinVarVariant:36092","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:53574","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"ClinVarVariant:158741","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:12780","phenotype":{"types":[{"id":"HP:0006880","label":"Cerebellar hemangioblastoma"}]}},{"entity":"ClinVarVariant:21545","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1436","phenotype":{"types":[{"id":"ZP:0007196","label":"abnormal(ly) structure optic tract"}]}},{"entity":"ClinVarVariant:167709","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:35830","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:49922","phenotype":{"types":[{"id":"HP:0006772","label":"Renal angiomyolipoma"}]}},{"entity":"ClinVarVariant:6384","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"MGI:1933835","phenotype":{"types":[{"id":"MP:0010500","label":"myocardium hypoplasia"}]}},{"entity":"MGI:1857208","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:67907","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"FlyBase:FBal0210831","phenotype":{"types":[{"id":"FBcv:0000665","label":"body size defective"}]}},{"entity":"ClinVarVariant:136160","phenotype":{"types":[{"id":"HP:0001679","label":"Abnormality of the aorta"}]}},{"entity":"AQTL:39150","phenotype":{"types":[{"id":"AQTLTrait:1096","label":"Teat length"}]}},{"entity":"ClinVarVariant:48426","phenotype":{"types":[{"id":"HP:0010780","label":"Hyperacusis"}]}},{"entity":"ClinVarVariant:100768","phenotype":{"types":[{"id":"HP:0011448","label":"Ankle clonus"}]}},{"entity":"ClinVarVariant:158764","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"dbSNP:rs1934954","phenotype":{"types":[{"id":"HP:0000988","label":"Skin rash"}]}},{"entity":"ClinVarVariant:53774","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:1965","phenotype":{"types":[{"id":"HP:0001890","label":"Autoimmune hemolytic anemia"}]}},{"entity":"ClinVarVariant:215590","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:6542","phenotype":{"types":[{"id":"HP:0002213","label":"Fine hair"}]}},{"entity":"ClinVarVariant:39867","phenotype":{"types":[{"id":"HP:0002910","label":"Elevated hepatic transaminases"}]}},{"entity":"ClinVarVariant:53327","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"ClinVarVariant:14005","phenotype":{"types":[{"id":"HP:0100783","label":"Breast aplasia"}]}},{"entity":"ClinVarVariant:189048","phenotype":{"types":[{"id":"HP:0005598","label":"Facial telangiectasia in butterfly midface distribution"}]}},{"entity":"ZFIN:ZDB-ALT-051223-6","phenotype":{"types":[{"id":"ZP:0011581","label":"abnormal(ly) malformed post-vent vasculature"}]}},{"entity":"ClinVarVariant:16685","phenotype":{"types":[{"id":"HP:0002027","label":"Abdominal pain"}]}},{"entity":"ClinVarVariant:9659","phenotype":{"types":[{"id":"HP:0002891","label":"Uterine leiomyosarcoma"}]}},{"entity":"MGI:1857211","phenotype":{"types":[{"id":"MP:0008070","label":"absent T cells"}]}},{"entity":"ClinVarVariant:13370","phenotype":{"types":[{"id":"HP:0001894","label":"Thrombocytosis"}]}},{"entity":"ClinVarVariant:53565","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"ClinVarVariant:216937","phenotype":{"types":[{"id":"HP:0006960","label":"Choroid plexus calcification"}]}},{"entity":"MGI:3529581","phenotype":{"types":[{"id":"MP:0009967","label":"abnormal neuron proliferation"}]}},{"entity":"MGI:2156458","phenotype":{"types":[{"id":"HP:0006270","label":"Hypoplastic spleen"}]}},{"entity":"ClinVarVariant:68700","phenotype":{"types":[{"id":"HP:0000843","label":"Hyperparathyroidism"}]}},{"entity":"ClinVarVariant:53326","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:161123","phenotype":{"types":[{"id":"HP:0000496","label":"Abnormality of eye movement"}]}},{"entity":"ClinVarVariant:10486","phenotype":{"types":[{"id":"HP:0001922","label":"Vacuolated lymphocytes"}]}},{"entity":"ClinVarVariant:53236","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:24442","phenotype":{"types":[{"id":"HP:0008619","label":"Bilateral sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:4617","phenotype":{"types":[{"id":"HP:0003390","label":"Sensory axonal neuropathy"}]}},{"entity":"ClinVarVariant:101415","phenotype":{"types":[{"id":"HP:0000963","label":"Thin skin"}]}},{"entity":"FlyBase:FBal0239918","phenotype":{"types":[{"id":"FBcv:0000408","label":"stress response defective"}]}},{"entity":"ClinVarVariant:42377","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"dbSNP:rs110204815","phenotype":{"types":[{"id":"AQTLTrait:1081","label":"Age at puberty"}]}},{"entity":"ClinVarVariant:3694","phenotype":{"types":[{"id":"HP:0001114","label":"Xanthelasma"}]}},{"entity":"FlyBase:FBal0038994","phenotype":{"types":[{"id":"FBbt:00002142PHENOTYPE","label":"Drosophila metathoracic intersegmental nerve phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008852-WBRNAi00093225","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"ClinVarVariant:35521","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:36133","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:181833","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"ClinVarVariant:25300","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"AQTL:23571","phenotype":{"types":[{"id":"AQTLTrait:2252","label":"LDL cholesterol level"}]}},{"entity":"ClinVarVariant:159421","phenotype":{"types":[{"id":"HP:0100627","label":"Displacement of the external urethral meatus"}]}},{"entity":"MGI:2389580","phenotype":{"types":[{"id":"MP:0000952","label":"abnormal CNS glial cell morphology"}]}},{"entity":"ClinVarVariant:100651","phenotype":{"types":[{"id":"HP:0002553","label":"Highly arched eyebrow"}]}},{"entity":"FlyBase:FBal0277412","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:135775","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:189124","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:42053","phenotype":{"types":[{"id":"HP:0003281","label":"Increased serum ferritin"}]}},{"entity":"ClinVarVariant:18426","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:5965","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"ClinVarVariant:10867","phenotype":{"types":[{"id":"HP:0010972","label":"Anemia of inadequate production"}]}},{"entity":"ClinVarVariant:24410","phenotype":{"types":[{"id":"HP:0100633","label":"Esophagitis"}]}},{"entity":"AQTL:7240","phenotype":{"types":[{"id":"AQTLTrait:554","label":"Anal atresia"}]}},{"entity":"ClinVarVariant:97813","phenotype":{"types":[{"id":"HP:0001974","label":"Leukocytosis"}]}},{"entity":"ClinVarVariant:3642","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:49340","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"ClinVarVariant:24295","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"MGI:4849540","phenotype":{"types":[{"id":"MP:0009420","label":"skeletal muscle endomysial fibrosis"}]}},{"entity":"FlyBase:FBal0204839","phenotype":{"types":[{"id":"FBbt:00004729PHENOTYPE","label":"Drosophila wing phenotype"}]}},{"entity":"ClinVarVariant:96617","phenotype":{"types":[{"id":"HP:0006846","label":"Acute encephalopathy"}]}},{"entity":"ClinVarVariant:135766","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:38889","phenotype":{"types":[{"id":"HP:0002634","label":"Arteriosclerosis"}]}},{"entity":"MGI:1856150","phenotype":{"types":[{"id":"MP:0000159","label":"abnormal xiphoid process morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004887-WBRNAi00030287","phenotype":{"types":[{"id":"WBPhenotype:0000054","label":"larval lethal"}]}},{"entity":"ClinVarVariant:15282","phenotype":{"types":[{"id":"HP:0005505","label":"Refractory anemia"}]}},{"entity":"ClinVarVariant:21759","phenotype":{"types":[{"id":"HP:0002411","label":"Myokymia"}]}},{"entity":"AQTL:42663","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"ClinVarVariant:11445","phenotype":{"types":[{"id":"HP:0002136","label":"Broad-based gait"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001486-WBRNAi00102268","phenotype":{"types":[{"id":"WBPhenotype:0001900","label":"reduced levels of reduced glutathione"}]}},{"entity":"ClinVarVariant:194287","phenotype":{"types":[{"id":"HP:0004404","label":"Abnormality of the nipple"}]}},{"entity":"ClinVarVariant:167080","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:65853","phenotype":{"types":[{"id":"HP:0001274","label":"Agenesis of corpus callosum"}]}},{"entity":"ClinVarVariant:101152","phenotype":{"types":[{"id":"HP:0000490","label":"Deeply set eye"}]}},{"entity":"ClinVarVariant:180194","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"ClinVarVariant:60506","phenotype":{"types":[{"id":"HP:0003510","label":"Severe short stature"}]}},{"entity":"ClinVarVariant:159910","phenotype":{"types":[{"id":"HP:0003881","label":"Humeral sclerosis"}]}},{"entity":"FlyBase:FBal0244148","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:53229","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"AQTL:408","phenotype":{"types":[{"id":"AQTLTrait:2056","label":"Skin fat weight"}]}},{"entity":"NCBIGene:100302680","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"MGI:4429538","phenotype":{"types":[{"id":"MP:0008025","label":"brain vacuoles"}]}},{"entity":"ClinVarVariant:65014","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:162525","phenotype":{"types":[{"id":"HP:0008281","label":"Acute hyperammonemia"}]}},{"entity":"ClinVarVariant:157514","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001177-WBRNAi00061092","phenotype":{"types":[{"id":"WBPhenotype:0000279","label":"spicule insertion defective"}]}},{"entity":"FlyBase:FBal0258005","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:53758","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:53983","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:53422","phenotype":{"types":[{"id":"HP:0001948","label":"Alkalosis"}]}},{"entity":"FlyBase:FBal0042573","phenotype":{"types":[{"id":"FBbt:00000008PHENOTYPE","label":"Drosophila labral segment phenotype"}]}},{"entity":"ClinVarVariant:41171","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:188881","phenotype":{"types":[{"id":"HP:0001874","label":"Abnormality of neutrophils"}]}},{"entity":"ClinVarVariant:40291","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:7502","phenotype":{"types":[{"id":"HP:0007468","label":"Perifollicular hyperkeratosis"}]}},{"entity":"ClinVarVariant:7725","phenotype":{"types":[{"id":"HP:0007552","label":"Abnormal subcutaneous fat tissue distribution"}]}},{"entity":"ClinVarVariant:11577","phenotype":{"types":[{"id":"HP:0007018","label":"Attention deficit hyperactivity disorder"}]}},{"entity":"MGI:3771073","phenotype":{"types":[{"id":"MP:0003017","label":"decreased circulating bicarbonate level"}]}},{"entity":"ClinVarVariant:13335","phenotype":{"types":[{"id":"HP:0001644","label":"Dilated cardiomyopathy"}]}},{"entity":"ClinVarVariant:53336","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:49180","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:52318","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"MGI:1857270","phenotype":{"types":[{"id":"MP:0002655","label":"abnormal keratinocyte morphology"}]}},{"entity":"ClinVarVariant:161210","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:162038","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:31100","phenotype":{"types":[{"id":"HP:0002558","label":"Supernumerary nipple"}]}},{"entity":"ClinVarVariant:41098","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:167222","phenotype":{"types":[{"id":"HP:0002566","label":"Intestinal malrotation"}]}},{"entity":"ClinVarVariant:216765","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:10753","phenotype":{"types":[{"id":"HP:0012622","label":"Chronic kidney disease"}]}},{"entity":"ClinVarVariant:53982","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:184580","phenotype":{"types":[{"id":"HP:0100777","label":"Exostoses"}]}},{"entity":"ClinVarVariant:8986","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007704-WBRNAi00066087","phenotype":{"types":[{"id":"WBPhenotype:0000541","label":"cord commissures fail to reach target"}]}},{"entity":"MGI:2681122","phenotype":{"types":[{"id":"MP:0003868","label":"abnormal feces composition"}]}},{"entity":"dbSNP:rs6538140","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:53000","phenotype":{"types":[{"id":"HP:0000598","label":"Abnormality of the ear"}]}},{"entity":"ClinVarVariant:158819","phenotype":{"types":[{"id":"HP:0000340","label":"Sloping forehead"}]}},{"entity":"ClinVarVariant:15202","phenotype":{"types":[{"id":"HP:0008151","label":"Prolonged prothrombin time"}]}},{"entity":"MGI:2385836","phenotype":{"types":[{"id":"MP:0004087","label":"abnormal muscle fiber morphology"}]}},{"entity":"ClinVarVariant:3961","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:38352","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:8870","phenotype":{"types":[{"id":"HP:0001216","label":"Delayed ossification of carpal bones"}]}},{"entity":"ClinVarVariant:10053","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:49410","phenotype":{"types":[{"id":"HP:0002617","label":"Aneurysm"}]}},{"entity":"ClinVarVariant:49858","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"MGI:3838346","phenotype":{"types":[{"id":"MP:0003917","label":"increased kidney weight"}]}},{"entity":"MGI:2181194","phenotype":{"types":[{"id":"MP:0010970","label":"abnormal compact bone lamellar structure"}]}},{"entity":"ClinVarVariant:53813","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:6278","phenotype":{"types":[{"id":"HP:0011362","label":"Abnormal hair quantity"}]}},{"entity":"ClinVarVariant:24558","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"MGI:4843437","phenotype":{"types":[{"id":"MP:0010268","label":"decreased lymphoma incidence"}]}},{"entity":"ClinVarVariant:7993","phenotype":{"types":[{"id":"HP:0000912","label":"Sprengel anomaly"}]}},{"entity":"ClinVarVariant:11313","phenotype":{"types":[{"id":"HP:0003455","label":"Elevated long chain fatty acids"}]}},{"entity":"AQTL:13657","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"ClinVarVariant:66802","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:42315","phenotype":{"types":[{"id":"HP:0004933","label":"Ascending aortic dissection"}]}},{"entity":"ClinVarVariant:2827","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"ClinVarVariant:127449","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"MGI:3845884","phenotype":{"types":[{"id":"MP:0008019","label":"increased liver tumor incidence"}]}},{"entity":"ClinVarVariant:210769","phenotype":{"types":[{"id":"HP:0000336","label":"Prominent supraorbital ridges"}]}},{"entity":"ClinVarVariant:14051","phenotype":{"types":[{"id":"HP:0002359","label":"Frequent falls"}]}},{"entity":"ClinVarVariant:7224","phenotype":{"types":[{"id":"HP:0100651","label":"Type I diabetes mellitus"}]}},{"entity":"ClinVarVariant:196495","phenotype":{"types":[{"id":"HP:0002179","label":"Opisthotonus"}]}},{"entity":"ClinVarVariant:24621","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:201582","phenotype":{"types":[{"id":"HP:0100749","label":"Chest pain"}]}},{"entity":"ClinVarVariant:38322","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"MGI:1856691","phenotype":{"types":[{"id":"MP:0011101","label":"prenatal lethality, incomplete penetrance"}]}},{"entity":"ClinVarVariant:12207","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"ClinVarVariant:5028","phenotype":{"types":[{"id":"HP:0000230","label":"Gingivitis"}]}},{"entity":"MGI:3574072","phenotype":{"types":[{"id":"GO:0014037PHENOTYPE","label":"Schwann cell differentiation phenotype"}]}},{"entity":"FlyBase:FBal0206015","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:52308","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:53376","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:135892","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"AQTL:9532","phenotype":{"types":[{"id":"AQTLTrait:2029","label":"Tibia bone mineral content"}]}},{"entity":"ClinVarVariant:82771","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"ClinVarVariant:53264","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"FlyBase:FBal0218574","phenotype":{"types":[{"id":"FBbt:00004889PHENOTYPE","label":"karyosome phenotype"}]}},{"entity":"ClinVarVariant:35967","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"dbSNP:rs17135859","phenotype":{"types":[{"id":"HP:0002140","label":"Ischemic stroke"}]}},{"entity":"ClinVarVariant:159941","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"MGI:2181294","phenotype":{"types":[{"id":"MP:0009409","label":"abnormal skeletal muscle fiber type ratio"}]}},{"entity":"ClinVarVariant:211646","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"MGI:5056148","phenotype":{"types":[{"id":"MP:0001923","label":"reduced female fertility"}]}},{"entity":"ClinVarVariant:6711","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:163766","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ZFIN:ZDB-ALT-091112-20","phenotype":{"types":[{"id":"ZP:0001833","label":"abnormal(ly) deformed cranial cartilage"}]}},{"entity":"ClinVarVariant:39297","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"MGI:5441069","phenotype":{"types":[{"id":"MP:0004046","label":"abnormal mitosis"}]}},{"entity":"ClinVarVariant:24468","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:216732","phenotype":{"types":[{"id":"HP:0001541","label":"Ascites"}]}},{"entity":"FlyBase:FBal0316487","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"MGI:2183949","phenotype":{"types":[{"id":"MP:0003786","label":"premature aging"}]}},{"entity":"ClinVarVariant:41161","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:36567","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:24386","phenotype":{"types":[{"id":"HP:0008063","label":"Aplasia/Hypoplasia of the lens"}]}},{"entity":"AQTL:10182","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:158363","phenotype":{"types":[{"id":"HP:0000742","label":"Self-mutilation"}]}},{"entity":"ClinVarVariant:100721","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"MGI:3664305","phenotype":{"types":[{"id":"MP:0003137","label":"abnormal impulse conducting system conduction"}]}},{"entity":"ClinVarVariant:17282","phenotype":{"types":[{"id":"HP:0002273","label":"Tetraparesis"}]}},{"entity":"ClinVarVariant:159049","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:21789","phenotype":{"types":[{"id":"HP:0002411","label":"Myokymia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004726-WBRNAi00008634","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:4531","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:36309","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"ClinVarVariant:4367","phenotype":{"types":[{"id":"HP:0001776","label":"Bilateral talipes equinovarus"}]}},{"entity":"ClinVarVariant:67986","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:41142","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-030616-579-ZDB-MRPHLNO-070531-6","phenotype":{"types":[{"id":"GO:0031016PHENOTYPE","label":"pancreas development phenotype"}]}},{"entity":"ClinVarVariant:31224","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:199204","phenotype":{"types":[{"id":"HP:0002153","label":"Hyperkalemia"}]}},{"entity":"ClinVarVariant:13419","phenotype":{"types":[{"id":"HP:0002315","label":"Headache"}]}},{"entity":"ClinVarVariant:64785","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:198957","phenotype":{"types":[{"id":"HP:0010454","label":"Acetabular spurs"}]}},{"entity":"ClinVarVariant:6542","phenotype":{"types":[{"id":"HP:0007476","label":"Anhidrotic ectodermal dysplasia"}]}},{"entity":"ClinVarVariant:2648","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"FlyBase:FBal0051173","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:10766","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"AQTL:8854","phenotype":{"types":[{"id":"AQTLTrait:491","label":"Ear size"}]}},{"entity":"ClinVarVariant:136109","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:29986","phenotype":{"types":[{"id":"HP:0001376","label":"Limitation of joint mobility"}]}},{"entity":"ClinVarVariant:211645","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"ClinVarVariant:158349","phenotype":{"types":[{"id":"HP:0000343","label":"Long philtrum"}]}},{"entity":"ClinVarVariant:134889","phenotype":{"types":[{"id":"HP:0100634","label":"Neuroendocrine neoplasm"}]}},{"entity":"ClinVarVariant:10738","phenotype":{"types":[{"id":"HP:0100699","label":"Scarring"}]}},{"entity":"FlyBase:FBal0209081","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:190276","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"ClinVarVariant:14271","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:204288","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:155948","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:48922","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"ClinVarVariant:83179","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"ClinVarVariant:30382","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:204092","phenotype":{"types":[{"id":"HP:0009830","label":"Peripheral neuropathy"}]}},{"entity":"ClinVarVariant:13714","phenotype":{"types":[{"id":"HP:0002155","label":"Hypertriglyceridemia"}]}},{"entity":"ClinVarVariant:10130","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022792-WBRNAi00100525","phenotype":{"types":[{"id":"WBPhenotype:0000154","label":"reduced brood size"}]}},{"entity":"ClinVarVariant:38788","phenotype":{"types":[{"id":"HP:0011507","label":"Macular flecks"}]}},{"entity":"ClinVarVariant:16636","phenotype":{"types":[{"id":"HP:0007110","label":"Central hypoventilation"}]}},{"entity":"ClinVarVariant:215714","phenotype":{"types":[{"id":"HP:0002076","label":"Migraine"}]}},{"entity":"ClinVarVariant:92913","phenotype":{"types":[{"id":"HP:0100670","label":"Rough bone trabeculation"}]}},{"entity":"ClinVarVariant:142700","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:161996","phenotype":{"types":[{"id":"HP:0006538","label":"Recurrent bronchopulmonary infections"}]}},{"entity":"ClinVarVariant:162456","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:195849","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"AQTL:27763","phenotype":{"types":[{"id":"AQTLTrait:1485","label":"Mean corpuscular volume"}]}},{"entity":"ClinVarVariant:41168","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"AQTL:44243","phenotype":{"types":[{"id":"AQTLTrait:1136","label":"Bone quality"}]}},{"entity":"MGI:3772332","phenotype":{"types":[{"id":"MP:0000490","label":"abnormal crypts of Lieberkuhn morphology"}]}},{"entity":"ClinVarVariant:38414","phenotype":{"types":[{"id":"HP:0100790","label":"Hernia"}]}},{"entity":"ClinVarVariant:48957","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:65312","phenotype":{"types":[{"id":"HP:0000826","label":"Precocious puberty"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-060908-2-ZDB-MRPHLNO-100616-1","phenotype":{"types":[{"id":"ZP:0001349","label":"abnormal(ly) apoptotic eye"}]}},{"entity":"ClinVarVariant:5595","phenotype":{"types":[{"id":"HP:0002013","label":"Vomiting"}]}},{"entity":"AQTL:32791","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:160181","phenotype":{"types":[{"id":"HP:0001321","label":"Cerebellar hypoplasia"}]}},{"entity":"AQTL:53986","phenotype":{"types":[{"id":"AQTLTrait:1153","label":"Stillbirth"}]}},{"entity":"ClinVarVariant:10733","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"ClinVarVariant:49640","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:217079","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:97787","phenotype":{"types":[{"id":"HP:0100603","label":"Toxemia of pregnancy"}]}},{"entity":"ClinVarVariant:97554","phenotype":{"types":[{"id":"HP:0100769","label":"Synovitis"}]}},{"entity":"ClinVarVariant:11060","phenotype":{"types":[{"id":"HP:0002021","label":"Pyloric stenosis"}]}},{"entity":"ClinVarVariant:53357","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"ClinVarVariant:210443","phenotype":{"types":[{"id":"HP:0100545","label":"Arterial stenosis"}]}},{"entity":"MGI:4453204","phenotype":{"types":[{"id":"MP:0001922","label":"reduced male fertility"}]}},{"entity":"ClinVarVariant:35833","phenotype":{"types":[{"id":"HP:0001742","label":"Nasal obstruction"}]}},{"entity":"MGI:1856066","phenotype":{"types":[{"id":"HP:0011096","label":"Peripheral demyelination"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004919-WBRNAi00071373","phenotype":{"types":[{"id":"WBPhenotype:0000258","label":"cell secretion variant"}]}},{"entity":"ClinVarVariant:38626","phenotype":{"types":[{"id":"HP:0001578","label":"Hypercortisolism"}]}},{"entity":"ClinVarVariant:31676","phenotype":{"types":[{"id":"HP:0000448","label":"Prominent nose"}]}},{"entity":"MGI:3614434","phenotype":{"types":[{"id":"MP:0005536","label":"Leydig cell hypoplasia"}]}},{"entity":"ClinVarVariant:21358","phenotype":{"types":[{"id":"HP:0002553","label":"Highly arched eyebrow"}]}},{"entity":"ClinVarVariant:126095","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:3382","phenotype":{"types":[{"id":"HP:0006485","label":"Agenesis of incisor"}]}},{"entity":"ClinVarVariant:185554","phenotype":{"types":[{"id":"HP:0006721","label":"Acute lymphoblastic leukemia"}]}},{"entity":"FlyBase:FBal0135765","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"AQTL:6504","phenotype":{"types":[{"id":"AQTLTrait:2021","label":"Humerus length"}]}},{"entity":"ClinVarVariant:42385","phenotype":{"types":[{"id":"HP:0100719","label":"Lens coloboma"}]}},{"entity":"ClinVarVariant:53360","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:127117","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:25201","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"ClinVarVariant:189862","phenotype":{"types":[{"id":"HP:0002384","label":"Focal seizures with impairment of consciousness or awareness"}]}},{"entity":"ClinVarVariant:183683","phenotype":{"types":[{"id":"HP:0003164","label":"Hypothalamic gonadotropin-releasing hormone (GNRH) deficiency"}]}},{"entity":"ClinVarVariant:159370","phenotype":{"types":[{"id":"HP:0009890","label":"High anterior hairline"}]}},{"entity":"ClinVarVariant:216775","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"MGI:4364913","phenotype":{"types":[{"id":"MP:0006411","label":"upturned snout"}]}},{"entity":"MGI:1857852","phenotype":{"types":[{"id":"MP:0000872","label":"abnormal cerebellum external granule cell layer morphology"}]}},{"entity":"ClinVarVariant:215957","phenotype":{"types":[{"id":"HP:0005344","label":"Abnormality of the carotid arteries"}]}},{"entity":"MGI:3777145","phenotype":{"types":[{"id":"MP:0001981","label":"increased chemically-elicited antinociception"}]}},{"entity":"ClinVarVariant:65753","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:56716","phenotype":{"types":[{"id":"HP:0002074","label":"Increased neuronal autofluorescent lipopigment"}]}},{"entity":"ClinVarVariant:6643","phenotype":{"types":[{"id":"HP:0004944","label":"Cerebral aneurysm"}]}},{"entity":"ClinVarVariant:143406","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003920-WBRNAi00069781","phenotype":{"types":[{"id":"WBPhenotype:0000061","label":"extended life span"}]}},{"entity":"ClinVarVariant:7623","phenotype":{"types":[{"id":"HP:0001297","label":"Stroke"}]}},{"entity":"ZFIN:ZDB-ALT-040824-2","phenotype":{"types":[{"id":"ZP:0000961","label":"abnormal(ly) bent trunk"}]}},{"entity":"ClinVarVariant:35839","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:158283","phenotype":{"types":[{"id":"HP:0001888","label":"Lymphopenia"}]}},{"entity":"AQTL:31062","phenotype":{"types":[{"id":"AQTLTrait:1169","label":"Interval to first estrus after calving"}]}},{"entity":"ClinVarVariant:11454","phenotype":{"types":[{"id":"HP:0000971","label":"Abnormality of the sweat gland"}]}},{"entity":"ClinVarVariant:17349","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"MGI:1927183","phenotype":{"types":[{"id":"MP:0008571","label":"abnormal synaptic bouton morphology"}]}},{"entity":"ClinVarVariant:211736","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:54175","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:132825","phenotype":{"types":[{"id":"HP:0002140","label":"Ischemic stroke"}]}},{"entity":"MGI:3620102","phenotype":{"types":[{"id":"MP:0003887","label":"increased hepatocyte apoptosis"}]}},{"entity":"MGI:2450309","phenotype":{"types":[{"id":"MP:0000260","label":"abnormal angiogenesis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001691-WBRNAi00076971","phenotype":{"types":[{"id":"WBPhenotype:0000280","label":"breaks in alae"}]}},{"entity":"ClinVarVariant:97923","phenotype":{"types":[{"id":"HP:0001917","label":"Renal amyloidosis"}]}},{"entity":"FlyBase:FBal0138238","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:88857","phenotype":{"types":[{"id":"HP:0000787","label":"Nephrolithiasis"}]}},{"entity":"ClinVarVariant:788","phenotype":{"types":[{"id":"HP:0001640","label":"Cardiomegaly"}]}},{"entity":"ClinVarVariant:11901","phenotype":{"types":[{"id":"HP:0008169","label":"Reduced factor VII activity"}]}},{"entity":"MGI:2388055","phenotype":{"types":[{"id":"MP:0005325","label":"abnormal renal glomerulus morphology"}]}},{"entity":"ClinVarVariant:30944","phenotype":{"types":[{"id":"HP:0003026","label":"Short long bone"}]}},{"entity":"ClinVarVariant:1483","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:1369","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:41065","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:10108","phenotype":{"types":[{"id":"HP:0100726","label":"Kaposi's sarcoma"}]}},{"entity":"ClinVarVariant:10757","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"ClinVarVariant:210471","phenotype":{"types":[{"id":"HP:0002208","label":"Coarse hair"}]}},{"entity":"AQTL:12523","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"dbSNP:rs12294076","phenotype":{"types":[{"id":"HP:0000211","label":"Trismus"}]}},{"entity":"ClinVarVariant:4221","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:159447","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"MGI:4432654","phenotype":{"types":[{"id":"MP:0003131","label":"increased erythrocyte cell number"}]}},{"entity":"ClinVarVariant:216216","phenotype":{"types":[{"id":"HP:0003254","label":"Abnormality of DNA repair"}]}},{"entity":"ClinVarVariant:42397","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"MGI:1933764","phenotype":{"types":[{"id":"MP:0000814","label":"absent dentate gyrus"}]}},{"entity":"ClinVarVariant:5487","phenotype":{"types":[{"id":"HP:0011958","label":"Retinal perforation"}]}},{"entity":"ClinVarVariant:158894","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:10987","phenotype":{"types":[{"id":"HP:0003217","label":"Hyperglutaminemia"}]}},{"entity":"ClinVarVariant:53294","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:10124","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:30491","phenotype":{"types":[{"id":"HP:0003765","label":"Psoriasis"}]}},{"entity":"ClinVarVariant:189593","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:68497","phenotype":{"types":[{"id":"HP:0001047","label":"Atopic dermatitis"}]}},{"entity":"ClinVarVariant:210028","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:9922","phenotype":{"types":[{"id":"HP:0010529","label":"Echolalia"}]}},{"entity":"ClinVarVariant:42017","phenotype":{"types":[{"id":"HP:0000951","label":"Abnormality of the skin"}]}},{"entity":"ClinVarVariant:35887","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"ClinVarVariant:143254","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"ZFIN:ZDB-ALT-121210-2","phenotype":{"types":[{"id":"ZP:0012714","label":"abnormal(ly) mislocalised pancreas neutrophil"}]}},{"entity":"ClinVarVariant:53973","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:99926","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:39637","phenotype":{"types":[{"id":"HP:0000405","label":"Conductive hearing impairment"}]}},{"entity":"ClinVarVariant:30547","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ClinVarVariant:36051","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:11592","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"ClinVarVariant:4301","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:42066","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:41149","phenotype":{"types":[{"id":"HP:0000668","label":"Hypodontia"}]}},{"entity":"MGI:1856601","phenotype":{"types":[{"id":"MP:0009474","label":"thick epidermis stratum spinosum"}]}},{"entity":"ClinVarVariant:38306","phenotype":{"types":[{"id":"HP:0008551","label":"Microtia"}]}},{"entity":"ClinVarVariant:1957","phenotype":{"types":[{"id":"HP:0002644","label":"Abnormality of pelvic girdle bone morphology"}]}},{"entity":"ClinVarVariant:24677","phenotype":{"types":[{"id":"HP:0100633","label":"Esophagitis"}]}},{"entity":"ClinVarVariant:179546","phenotype":{"types":[{"id":"HP:0002017","label":"Nausea and vomiting"}]}},{"entity":"ClinVarVariant:189086","phenotype":{"types":[{"id":"HP:0000400","label":"Macrotia"}]}},{"entity":"ClinVarVariant:1450","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"MGI:5513765","phenotype":{"types":[{"id":"MP:0005635","label":"decreased circulating bilirubin level"}]}},{"entity":"ClinVarVariant:53628","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:126974","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:199200","phenotype":{"types":[{"id":"HP:0012043","label":"Pendular nystagmus"}]}},{"entity":"ClinVarVariant:53703","phenotype":{"types":[{"id":"HP:0100660","label":"Dyskinesia"}]}},{"entity":"MGI:3695897","phenotype":{"types":[{"id":"MP:0000755","label":"hindlimb paralysis"}]}},{"entity":"MGI:3040330","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"ClinVarVariant:7165","phenotype":{"types":[{"id":"HP:0001081","label":"Cholelithiasis"}]}},{"entity":"ClinVarVariant:5894","phenotype":{"types":[{"id":"HP:0000509","label":"Conjunctivitis"}]}},{"entity":"AQTL:26651","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:9617","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"FlyBase:FBal0261159","phenotype":{"types":[{"id":"FBcv:0000399","label":"courtship behavior defective"}]}},{"entity":"ClinVarVariant:159204","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:211653","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"MGI:2677447","phenotype":{"types":[{"id":"MP:0001825","label":"arrested T cell differentiation"}]}},{"entity":"ClinVarVariant:210388","phenotype":{"types":[{"id":"HP:0005054","label":"Metaphyseal spurs"}]}},{"entity":"ClinVarVariant:49421","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"ClinVarVariant:6459","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:5082","phenotype":{"types":[{"id":"HP:0003557","label":"Increased variability in muscle fiber diameter"}]}},{"entity":"ClinVarVariant:6582","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"ClinVarVariant:8884","phenotype":{"types":[{"id":"HP:0000567","label":"Chorioretinal coloboma"}]}},{"entity":"MGI:2179545","phenotype":{"types":[{"id":"MP:0002123","label":"abnormal definitive hematopoiesis"}]}},{"entity":"ClinVarVariant:53369","phenotype":{"types":[{"id":"HP:0000855","label":"Insulin resistance"}]}},{"entity":"MGI:2180680","phenotype":{"types":[{"id":"MP:0008188","label":"abnormal transitional stage B cell morphology"}]}},{"entity":"FlyBase:FBal0304813","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:49575","phenotype":{"types":[{"id":"HP:0009716","label":"Subependymal nodules"}]}},{"entity":"ClinVarVariant:1018","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:48862","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"MGI:2662305","phenotype":{"types":[{"id":"MP:0001622","label":"abnormal vasculogenesis"}]}},{"entity":"ClinVarVariant:39056","phenotype":{"types":[{"id":"HP:0003026","label":"Short long bone"}]}},{"entity":"ClinVarVariant:10743","phenotype":{"types":[{"id":"HP:0009763","label":"Limb pain"}]}},{"entity":"ClinVarVariant:44203","phenotype":{"types":[{"id":"HP:0007411","label":"Hypoplastic-absent sebaceous glands"}]}},{"entity":"MGI:1857291","phenotype":{"types":[{"id":"MP:0000628","label":"abnormal mammary gland development"}]}},{"entity":"ClinVarVariant:158724","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"MGI:2149065","phenotype":{"types":[{"id":"MP:0001900","label":"impaired synaptic plasticity"}]}},{"entity":"ClinVarVariant:97611","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"MGI:2176201","phenotype":{"types":[{"id":"MP:0003566","label":"abnormal cell adhesion"}]}},{"entity":"ClinVarVariant:24806","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ClinVarVariant:158359","phenotype":{"types":[{"id":"HP:0009765","label":"Low hanging columella"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003918-WBRNAi00083243","phenotype":{"types":[{"id":"WBPhenotype:0000425","label":"antibody staining reduced"}]}},{"entity":"ClinVarVariant:68536","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"FlyBase:FBal0059988","phenotype":{"types":[{"id":"FBbt:00004218PHENOTYPE","label":"Drosophila rhabdomere R3 phenotype"}]}},{"entity":"ClinVarVariant:53220","phenotype":{"types":[{"id":"HP:0006536","label":"Obstructive lung disease"}]}},{"entity":"ClinVarVariant:11550","phenotype":{"types":[{"id":"HP:0002747","label":"Respiratory insufficiency due to muscle weakness"}]}},{"entity":"WormBase:WBVar00252908","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:156338","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:31196","phenotype":{"types":[{"id":"HP:0003128","label":"Lactic acidosis"}]}},{"entity":"ClinVarVariant:10709","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"ClinVarVariant:65353","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:38749","phenotype":{"types":[{"id":"HP:0005101","label":"High-frequency hearing impairment"}]}},{"entity":"ClinVarVariant:53801","phenotype":{"types":[{"id":"HP:0006538","label":"Recurrent bronchopulmonary infections"}]}},{"entity":"ClinVarVariant:5561","phenotype":{"types":[{"id":"HP:0005227","label":"Adenomatous colonic polyposis"}]}},{"entity":"ClinVarVariant:136110","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:156138","phenotype":{"types":[{"id":"HP:0001319","label":"Neonatal hypotonia"}]}},{"entity":"ClinVarVariant:120246","phenotype":{"types":[{"id":"HP:0002162","label":"Low posterior hairline"}]}},{"entity":"ClinVarVariant:196277","phenotype":{"types":[{"id":"HP:0006510","label":"Chronic obstructive pulmonary disease"}]}},{"entity":"FlyBase:FBal0207442","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"dbSNP:rs41946434","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"MGI:2176172","phenotype":{"types":[{"id":"MP:0000876","label":"Purkinje cell degeneration"}]}},{"entity":"dbSNP:rs43488797","phenotype":{"types":[{"id":"AQTLTrait:1120","label":"Thurl width"}]}},{"entity":"ClinVarVariant:65533","phenotype":{"types":[{"id":"HP:0004432","label":"Agammaglobulinemia"}]}},{"entity":"ClinVarVariant:7706","phenotype":{"types":[{"id":"HP:0000114","label":"Proximal tubulopathy"}]}},{"entity":"ClinVarVariant:135896","phenotype":{"types":[{"id":"HP:0009733","label":"Glioma"}]}},{"entity":"ClinVarVariant:38975","phenotype":{"types":[{"id":"HP:0003236","label":"Elevated serum creatine phosphokinase"}]}},{"entity":"ClinVarVariant:1967","phenotype":{"types":[{"id":"HP:0002644","label":"Abnormality of pelvic girdle bone morphology"}]}},{"entity":"ClinVarVariant:127165","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:189084","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:1173","phenotype":{"types":[{"id":"HP:0008726","label":"Hypoplasia of the vagina"}]}},{"entity":"ClinVarVariant:15413","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"dbSNP:rs81307772","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"NCBIGene:100462676","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"AQTL:44219","phenotype":{"types":[{"id":"AQTLTrait:1173","label":"Rear leg set"}]}},{"entity":"FlyBase:FBal0284419","phenotype":{"types":[{"id":"FBbt:00003625PHENOTYPE","label":"Drosophila adult brain cell body rind phenotype"}]}},{"entity":"dbSNP:rs110474527","phenotype":{"types":[{"id":"AQTLTrait:1070","label":"Inseminations per conception"}]}},{"entity":"ClinVarVariant:13325","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:156338","phenotype":{"types":[{"id":"HP:0002863","label":"Myelodysplasia"}]}},{"entity":"ClinVarVariant:53718","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:208015","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"FlyBase:FBal0201465","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:41102","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:101364","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:35456","phenotype":{"types":[{"id":"HP:0002097","label":"Emphysema"}]}},{"entity":"WormBase:WBVar00087959","phenotype":{"types":[{"id":"WBPhenotype:0001645","label":"protein degradation variant"}]}},{"entity":"ClinVarVariant:120266","phenotype":{"types":[{"id":"HP:0001010","label":"Hypopigmentation of the skin"}]}},{"entity":"FlyBase:FBal0210406","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:10315","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:53332","phenotype":{"types":[{"id":"HP:0100889","label":"Abnormality of the ductus choledochus"}]}},{"entity":"ClinVarVariant:210467","phenotype":{"types":[{"id":"HP:0008070","label":"Sparse hair"}]}},{"entity":"ClinVarVariant:101212","phenotype":{"types":[{"id":"HP:0005267","label":"Premature delivery because of cervical insufficiency or membrane fragility"}]}},{"entity":"ClinVarVariant:24816","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ZFIN:ZDB-ALT-040716-2","phenotype":{"types":[{"id":"ZP:0006289","label":"abnormal(ly) detached from goblet cell towards intestinal epithelium"}]}},{"entity":"ClinVarVariant:65876","phenotype":{"types":[{"id":"HP:0009824","label":"Upper limb undergrowth"}]}},{"entity":"ClinVarVariant:24437","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"FlyBase:FBal0182631","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:53907","phenotype":{"types":[{"id":"HP:0005232","label":"Pancreatic dysplasia"}]}},{"entity":"FlyBase:FBal0211026","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:92734","phenotype":{"types":[{"id":"HP:0100324","label":"Scleroderma"}]}},{"entity":"ClinVarVariant:209982","phenotype":{"types":[{"id":"HP:0003487","label":"Babinski sign"}]}},{"entity":"ClinVarVariant:126869","phenotype":{"types":[{"id":"HP:0004724","label":"Calcium nephrolithiasis"}]}},{"entity":"ClinVarVariant:101374","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:42515","phenotype":{"types":[{"id":"HP:0000859","label":"Hyperaldosteronism"}]}},{"entity":"ClinVarVariant:188150","phenotype":{"types":[{"id":"HP:0009650","label":"Short distal phalanx of the thumb"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00044068-WBRNAi00075201","phenotype":{"types":[{"id":"WBPhenotype:0000154","label":"reduced brood size"}]}},{"entity":"ClinVarVariant:10457","phenotype":{"types":[{"id":"HP:0007763","label":"Retinal telangiectasia"}]}},{"entity":"ZFIN:ZDB-ALT-151110-1","phenotype":{"types":[{"id":"ZP:0002010","label":"abnormal(ly) morphology pancreas"}]}},{"entity":"FlyBase:FBal0208456","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:97422","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:7963","phenotype":{"types":[{"id":"HP:0010808","label":"Protruding tongue"}]}},{"entity":"ClinVarVariant:159677","phenotype":{"types":[{"id":"HP:0000368","label":"Low-set, posteriorly rotated ears"}]}},{"entity":"ClinVarVariant:21275","phenotype":{"types":[{"id":"HP:0011069","label":"Increased number of teeth"}]}},{"entity":"ClinVarVariant:39124","phenotype":{"types":[{"id":"HP:0006510","label":"Chronic obstructive pulmonary disease"}]}},{"entity":"ClinVarVariant:24454","phenotype":{"types":[{"id":"HP:0007763","label":"Retinal telangiectasia"}]}},{"entity":"MGI:3513254","phenotype":{"types":[{"id":"GO:0001756PHENOTYPE","label":"somitogenesis phenotype"}]}},{"entity":"ClinVarVariant:208427","phenotype":{"types":[{"id":"HP:0000926","label":"Platyspondyly"}]}},{"entity":"ClinVarVariant:3365","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:160227","phenotype":{"types":[{"id":"HP:0002070","label":"Limb ataxia"}]}},{"entity":"ClinVarVariant:53941","phenotype":{"types":[{"id":"HP:0003453","label":"Antineutrophil antibody positivity"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003020-WBRNAi00075368","phenotype":{"types":[{"id":"WBPhenotype:0000700","label":"multivulva"}]}},{"entity":"ClinVarVariant:161234","phenotype":{"types":[{"id":"HP:0007906","label":"Increased intraocular pressure"}]}},{"entity":"ClinVarVariant:217039","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"AQTL:23159","phenotype":{"types":[{"id":"AQTLTrait:2061","label":"Wing weight"}]}},{"entity":"MGI:3716711","phenotype":{"types":[{"id":"HP:0040189","label":"Scaling skin"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001832-WBRNAi00005000","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"WormBase:WBVar00087794","phenotype":{"types":[{"id":"WBPhenotype:0001683","label":"spermatogenesis defective hermaphrodite"}]}},{"entity":"AQTL:17561","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:11816","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:35572","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:211143","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"MGI:2180013","phenotype":{"types":[{"id":"MP:0001119","label":"abnormal female reproductive system morphology"}]}},{"entity":"FlyBase:FBal0296773","phenotype":{"types":[{"id":"FBbt:00004729PHENOTYPE","label":"Drosophila wing phenotype"}]}},{"entity":"ClinVarVariant:54008","phenotype":{"types":[{"id":"HP:0011850","label":"Parotitis"}]}},{"entity":"ClinVarVariant:183671","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"MGI:3615021","phenotype":{"types":[{"id":"HP:0004447","label":"Poikilocytosis"}]}},{"entity":"ClinVarVariant:18370","phenotype":{"types":[{"id":"HP:0000343","label":"Long philtrum"}]}},{"entity":"MGI:2429312","phenotype":{"types":[{"id":"MP:0006404","label":"abnormal lumbar dorsal root ganglion morphology"}]}},{"entity":"ClinVarVariant:10859","phenotype":{"types":[{"id":"HP:0010299","label":"Abnormality of dentin"}]}},{"entity":"ClinVarVariant:101185","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:3866","phenotype":{"types":[{"id":"HP:0002275","label":"Poor motor coordination"}]}},{"entity":"ClinVarVariant:42377","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"ClinVarVariant:55944","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:10728","phenotype":{"types":[{"id":"HP:0000763","label":"Sensory neuropathy"}]}},{"entity":"dbSNP:rs109894613","phenotype":{"types":[{"id":"AQTLTrait:1115","label":"Chest width"}]}},{"entity":"ClinVarVariant:92621","phenotype":{"types":[{"id":"HP:0003541","label":"Urinary glycosaminoglycan excretion"}]}},{"entity":"ClinVarVariant:31028","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"ZFIN:ZDB-ALT-090702-3","phenotype":{"types":[{"id":"ZP:0015766","label":"abnormal(ly) black mouth melanoma"}]}},{"entity":"ClinVarVariant:11734","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"FlyBase:FBal0194748","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:100637","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:135758","phenotype":{"types":[{"id":"HP:0008348","label":"Immunoglobulin IgG2 deficiency"}]}},{"entity":"ClinVarVariant:38922","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:10582","phenotype":{"types":[{"id":"HP:0005186","label":"Synovial hypertrophy"}]}},{"entity":"ClinVarVariant:216388","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:24677","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"MGI:3665249","phenotype":{"types":[{"id":"MP:0013744","label":"abnormal conjunctival sac morphology"}]}},{"entity":"ClinVarVariant:2715","phenotype":{"types":[{"id":"HP:0000992","label":"Cutaneous photosensitivity"}]}},{"entity":"ClinVarVariant:25244","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:161456","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:7165","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:10229","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:216144","phenotype":{"types":[{"id":"HP:0000090","label":"Nephronophthisis"}]}},{"entity":"MGI:3837303","phenotype":{"types":[{"id":"HP:0011116","label":"Abnormality of interferon secretion"}]}},{"entity":"ClinVarVariant:1460","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:56659","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004357-WBRNAi00085604","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:24792","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:135759","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"MGI:2682796","phenotype":{"types":[{"id":"MP:0003156","label":"abnormal leukocyte migration"}]}},{"entity":"ClinVarVariant:5946","phenotype":{"types":[{"id":"HP:0001260","label":"Dysarthria"}]}},{"entity":"ClinVarVariant:159201","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:49536","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:7401","phenotype":{"types":[{"id":"HP:0001100","label":"Heterochromia iridis"}]}},{"entity":"FlyBase:FBal0264413","phenotype":{"types":[{"id":"FBbt:00001896PHENOTYPE","label":"Drosophila embryonic/larval Malpighian tubule phenotype"}]}},{"entity":"ClinVarVariant:1049","phenotype":{"types":[{"id":"HP:0000682","label":"Abnormality of dental enamel"}]}},{"entity":"ClinVarVariant:67861","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"MGI:4288793","phenotype":{"types":[{"id":"HP:0000137","label":"Abnormality of the ovary"}]}},{"entity":"FlyBase:FBal0199496","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:53723","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"FlyBase:FBal0209583","phenotype":{"types":[{"id":"FBbt:00004580PHENOTYPE","label":"Drosophila mesothoracic tergum phenotype"}]}},{"entity":"ClinVarVariant:44810","phenotype":{"types":[{"id":"HP:0000465","label":"Webbed neck"}]}},{"entity":"ClinVarVariant:15485","phenotype":{"types":[{"id":"HP:0000786","label":"Primary amenorrhea"}]}},{"entity":"ClinVarVariant:216565","phenotype":{"types":[{"id":"HP:0005403","label":"T lymphocytopenia"}]}},{"entity":"ClinVarVariant:91690","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:92324","phenotype":{"types":[{"id":"HP:0000726","label":"Dementia"}]}},{"entity":"ClinVarVariant:24458","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"dbSNP:rs1075309","phenotype":{"types":[{"id":"HP:0011134","label":"Low-grade fever"}]}},{"entity":"ClinVarVariant:165011","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:8836","phenotype":{"types":[{"id":"HP:0011036","label":"Abnormality of renal excretion"}]}},{"entity":"ClinVarVariant:96439","phenotype":{"types":[{"id":"HP:0000457","label":"Depressed nasal ridge"}]}},{"entity":"ClinVarVariant:210712","phenotype":{"types":[{"id":"HP:0008572","label":"External ear malformation"}]}},{"entity":"ClinVarVariant:187907","phenotype":{"types":[{"id":"HP:0100786","label":"Hypersomnia"}]}},{"entity":"ClinVarVariant:53514","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"ClinVarVariant:159161","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"FlyBase:FBal0230433","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:35716","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:16678","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:10731","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:53667","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:211663","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"ClinVarVariant:5779","phenotype":{"types":[{"id":"HP:0000722","label":"Obsessive-compulsive behavior"}]}},{"entity":"ClinVarVariant:97644","phenotype":{"types":[{"id":"HP:0100539","label":"Periorbital edema"}]}},{"entity":"ClinVarVariant:159206","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:53393","phenotype":{"types":[{"id":"HP:0006706","label":"Cystic liver disease"}]}},{"entity":"ClinVarVariant:83176","phenotype":{"types":[{"id":"HP:0006740","label":"Transitional cell carcinoma of the bladder"}]}},{"entity":"ClinVarVariant:48917","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:216392","phenotype":{"types":[{"id":"HP:0001012","label":"Multiple lipomas"}]}},{"entity":"ClinVarVariant:161976","phenotype":{"types":[{"id":"HP:0001269","label":"Hemiparesis"}]}},{"entity":"ClinVarVariant:16993","phenotype":{"types":[{"id":"HP:0000691","label":"Microdontia"}]}},{"entity":"FlyBase:FBal0059537","phenotype":{"types":[{"id":"FBbt:00001730PHENOTYPE","label":"Drosophila larval head phenotype"}]}},{"entity":"ClinVarVariant:36475","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:159214","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:7155","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:11662","phenotype":{"types":[{"id":"HP:0000687","label":"Widely spaced teeth"}]}},{"entity":"ClinVarVariant:12002","phenotype":{"types":[{"id":"HP:0010980","label":"Hyperlipoproteinemia"}]}},{"entity":"NCBIGene:1913","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"ZFIN:ZDB-ALT-100409-2","phenotype":{"types":[{"id":"ZP:0016420","label":"abnormal(ly) has extra parts of type integument towards cell"}]}},{"entity":"ClinVarVariant:53894","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:167228","phenotype":{"types":[{"id":"HP:0000592","label":"Blue sclerae"}]}},{"entity":"ClinVarVariant:9429","phenotype":{"types":[{"id":"HP:0000632","label":"Lacrimation abnormality"}]}},{"entity":"dbSNP:rs6676375","phenotype":{"types":[{"id":"HP:0001254","label":"Lethargy"}]}},{"entity":"ClinVarVariant:100787","phenotype":{"types":[{"id":"HP:0009803","label":"Short phalanx of finger"}]}},{"entity":"ClinVarVariant:41422","phenotype":{"types":[{"id":"HP:0005855","label":"Multiple prenatal fractures"}]}},{"entity":"ZFIN:ZDB-ALT-070531-2","phenotype":{"types":[{"id":"ZP:0008366","label":"abnormal(ly) having decreased processual parts liver development towards cell proliferation"}]}},{"entity":"ClinVarVariant:97671","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"MGI:3814908","phenotype":{"types":[{"id":"HP:0010976","label":"B lymphocytopenia"}]}},{"entity":"ClinVarVariant:183069","phenotype":{"types":[{"id":"HP:0008256","label":"Adrenocortical adenoma"}]}},{"entity":"ClinVarVariant:56778","phenotype":{"types":[{"id":"HP:0002084","label":"Encephalocele"}]}},{"entity":"dbSNP:rs41697837","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:2588","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:184381","phenotype":{"types":[{"id":"HP:0002897","label":"Parathyroid adenoma"}]}},{"entity":"ClinVarVariant:135896","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"MGI:1857077","phenotype":{"types":[{"id":"MP:0013173","label":"trigeminal ganglion degeneration"}]}},{"entity":"ClinVarVariant:158776","phenotype":{"types":[{"id":"HP:0000826","label":"Precocious puberty"}]}},{"entity":"ClinVarVariant:1704","phenotype":{"types":[{"id":"HP:0003481","label":"Segmental peripheral demyelination/remyelination"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1302","phenotype":{"types":[{"id":"ZP:0000766","label":"abnormal(ly) bent post-vent region"}]}},{"entity":"ClinVarVariant:200395","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:126966","phenotype":{"types":[{"id":"HP:0001402","label":"Hepatocellular carcinoma"}]}},{"entity":"ClinVarVariant:1633","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"FlyBase:FBal0091132","phenotype":{"types":[{"id":"FBcv:0002027","label":"lethal - all die before end of pupal stage"}]}},{"entity":"ClinVarVariant:48892","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"ClinVarVariant:36061","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:5923","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"MGI:3826836","phenotype":{"types":[{"id":"MP:0009431","label":"decreased fetal weight"}]}},{"entity":"dbSNP:rs11886868","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:159683","phenotype":{"types":[{"id":"HP:0006461","label":"Proximal femoral epiphysiolysis"}]}},{"entity":"MGI:3762641","phenotype":{"types":[{"id":"MP:0011089","label":"perinatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:5545","phenotype":{"types":[{"id":"HP:0000972","label":"Palmoplantar hyperkeratosis"}]}},{"entity":"ClinVarVariant:13344","phenotype":{"types":[{"id":"HP:0000506","label":"Telecanthus"}]}},{"entity":"ClinVarVariant:3988","phenotype":{"types":[{"id":"HP:0006829","label":"Severe muscular hypotonia"}]}},{"entity":"ClinVarVariant:143170","phenotype":{"types":[{"id":"HP:0003474","label":"Sensory impairment"}]}},{"entity":"ClinVarVariant:49708","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:64689","phenotype":{"types":[{"id":"HP:0000445","label":"Wide nose"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006528-WBRNAi00085576","phenotype":{"types":[{"id":"WBPhenotype:0001982","label":"cell membrane organization biogenesis variant"}]}},{"entity":"ClinVarVariant:571","phenotype":{"types":[{"id":"HP:0000618","label":"Blindness"}]}},{"entity":"OMIM:226000","phenotype":{"types":[{"id":"HP:0001711","label":"Abnormality of the left ventricle"}]}},{"entity":"ClinVarVariant:209137","phenotype":{"types":[{"id":"HP:0001673","label":"Tachycardia (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:49501","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:7175","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:210451","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"MGI:3800176","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:120276","phenotype":{"types":[{"id":"HP:0001010","label":"Hypopigmentation of the skin"}]}},{"entity":"ClinVarVariant:24361","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"MGI:3527937","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:216466","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000065-WBRNAi00026399","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"AQTL:40844","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:10887","phenotype":{"types":[{"id":"HP:0002872","label":"Apneic episodes precipitated by illness, fatigue, stress"}]}},{"entity":"ClinVarVariant:10737","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001973-WBRNAi00063017","phenotype":{"types":[{"id":"WBPhenotype:0000709","label":"pharyngeal morphology variant"}]}},{"entity":"ClinVarVariant:3360","phenotype":{"types":[{"id":"HP:0009926","label":"Increased lacrimation"}]}},{"entity":"ClinVarVariant:54089","phenotype":{"types":[{"id":"HP:0001622","label":"Premature birth"}]}},{"entity":"FlyBase:FBal0051201","phenotype":{"types":[{"id":"FBbt:00003921PHENOTYPE","label":"optic chiasma phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000415-WBRNAi00097824","phenotype":{"types":[{"id":"WBPhenotype:0000243","label":"engulfment failure by killer cell"}]}},{"entity":"ClinVarVariant:56788","phenotype":{"types":[{"id":"HP:0002084","label":"Encephalocele"}]}},{"entity":"ClinVarVariant:35859","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:68302","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:209028","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"ClinVarVariant:18331","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:50912","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:634","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:53929","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ClinVarVariant:4330","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"ClinVarVariant:17521","phenotype":{"types":[{"id":"HP:0000127","label":"Renal salt wasting"}]}},{"entity":"MGI:3818518","phenotype":{"types":[{"id":"MP:0004179","label":"transmission ratio distortion"}]}},{"entity":"ClinVarVariant:3097","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"ClinVarVariant:14793","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:24745","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:215969","phenotype":{"types":[{"id":"HP:0007707","label":"Congenital primary aphakia"}]}},{"entity":"ClinVarVariant:12401","phenotype":{"types":[{"id":"HP:0002290","label":"Poliosis"}]}},{"entity":"FlyBase:FBal0199313","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"MGI:5086003","phenotype":{"types":[{"id":"MP:0010875","label":"increased bone volume"}]}},{"entity":"MGI:3707421","phenotype":{"types":[{"id":"MP:0003088","label":"abnormal prepulse inhibition"}]}},{"entity":"ClinVarVariant:55954","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:97691","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"NCBIGene:171","phenotype":{"types":[{"id":"HP:0001199","label":"Triphalangeal thumb"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004978-WBRNAi00084613","phenotype":{"types":[{"id":"WBPhenotype:0001719","label":"unfolded protein response variant"}]}},{"entity":"ClinVarVariant:143524","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"ClinVarVariant:3678","phenotype":{"types":[{"id":"HP:0002194","label":"Delayed gross motor development"}]}},{"entity":"FlyBase:FBal0040484","phenotype":{"types":[{"id":"FBbt:00001761PHENOTYPE","label":"Drosophila imaginal disc phenotype"}]}},{"entity":"ClinVarVariant:10176","phenotype":{"types":[{"id":"HP:0005268","label":"Spontaneous abortion"}]}},{"entity":"ClinVarVariant:49511","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:54082","phenotype":{"types":[{"id":"HP:0012236","label":"Elevated sweat chloride"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00021351-WBRNAi00080537","phenotype":{"types":[{"id":"WBPhenotype:0000154","label":"reduced brood size"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002324-WBRNAi00000137","phenotype":{"types":[{"id":"WBPhenotype:0000038","label":"exploded through vulva"}]}},{"entity":"MGI:1926955","phenotype":{"types":[{"id":"HP:0001067","label":"Neurofibromas"}]}},{"entity":"ClinVarVariant:101404","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:180631","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"ClinVarVariant:66441","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"ClinVarVariant:2241","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"FlyBase:FBal0062864","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:1730","phenotype":{"types":[{"id":"HP:0007503","label":"Generalized ichthyosis"}]}},{"entity":"ClinVarVariant:82791","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"ClinVarVariant:30189","phenotype":{"types":[{"id":"HP:0000845","label":"Growth hormone excess"}]}},{"entity":"ClinVarVariant:558","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:6718","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"MGI:2674242","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"MGI:3757609","phenotype":{"types":[{"id":"MP:0003107","label":"abnormal response to novelty"}]}},{"entity":"ClinVarVariant:7394","phenotype":{"types":[{"id":"HP:0002226","label":"White eyebrow"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003048-WBRNAi00062630","phenotype":{"types":[{"id":"WBPhenotype:0001102","label":"mitotic spindle defective early emb"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-061110-61-ZDB-MRPHLNO-120409-1","phenotype":{"types":[{"id":"ZP:0002202","label":"abnormal(ly) edematous whole organism"}]}},{"entity":"ClinVarVariant:3622","phenotype":{"types":[{"id":"HP:0007819","label":"Presenile cataracts"}]}},{"entity":"ClinVarVariant:188235","phenotype":{"types":[{"id":"HP:0100699","label":"Scarring"}]}},{"entity":"ClinVarVariant:40502","phenotype":{"types":[{"id":"HP:0000276","label":"Long face"}]}},{"entity":"ZFIN:ZDB-ALT-040723-8","phenotype":{"types":[{"id":"ZP:0002256","label":"abnormal(ly) distended fourth ventricle"}]}},{"entity":"FlyBase:FBal0143183","phenotype":{"types":[{"id":"FBbt:00004729PHENOTYPE","label":"Drosophila wing phenotype"}]}},{"entity":"ClinVarVariant:11657","phenotype":{"types":[{"id":"HP:0001187","label":"Hyperextensibility of the finger joints"}]}},{"entity":"ClinVarVariant:5462","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"MGI:4431999","phenotype":{"types":[{"id":"HP:0003228","label":"Hypernatremia"}]}},{"entity":"ClinVarVariant:30544","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:35755","phenotype":{"types":[{"id":"HP:0000426","label":"Prominent nasal bridge"}]}},{"entity":"MGI:2445946","phenotype":{"types":[{"id":"MP:0008392","label":"decreased primordial germ cell number"}]}},{"entity":"dbSNP:rs41933638","phenotype":{"types":[{"id":"AQTLTrait:1027","label":"Marbling score"}]}},{"entity":"ClinVarVariant:156148","phenotype":{"types":[{"id":"HP:0001319","label":"Neonatal hypotonia"}]}},{"entity":"ClinVarVariant:5041","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:66431","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"ClinVarVariant:68546","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:2767","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:135705","phenotype":{"types":[{"id":"HP:0100646","label":"Thyroiditis"}]}},{"entity":"FlyBase:FBal0203849","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:100931","phenotype":{"types":[{"id":"HP:0007359","label":"Focal seizures"}]}},{"entity":"MGI:3688879","phenotype":{"types":[{"id":"MP:0010392","label":"prolonged QRS complex duration"}]}},{"entity":"ClinVarVariant:35571","phenotype":{"types":[{"id":"HP:0003073","label":"Hypoalbuminemia"}]}},{"entity":"ClinVarVariant:24365","phenotype":{"types":[{"id":"HP:0000093","label":"Proteinuria"}]}},{"entity":"ClinVarVariant:24419","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:6114","phenotype":{"types":[{"id":"HP:0002510","label":"Spastic tetraplegia"}]}},{"entity":"ClinVarVariant:354","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:11634","phenotype":{"types":[{"id":"HP:0000395","label":"Prominent antihelix"}]}},{"entity":"MGI:3851113","phenotype":{"types":[{"id":"HP:0011472","label":"Abnormality of small intestinal villus morphology"}]}},{"entity":"ClinVarVariant:135899","phenotype":{"types":[{"id":"HP:0000902","label":"Rib fusion"}]}},{"entity":"ClinVarVariant:97681","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"MGI:1857166","phenotype":{"types":[{"id":"HP:0000099","label":"Glomerulonephritis"}]}},{"entity":"MGI:5465004","phenotype":{"types":[{"id":"MP:0011100","label":"preweaning lethality, complete penetrance"}]}},{"entity":"WormBase:WBVar00145415","phenotype":{"types":[{"id":"WBPhenotype:0000695","label":"vulva morphology variant"}]}},{"entity":"ClinVarVariant:189571","phenotype":{"types":[{"id":"HP:0200055","label":"Small hand"}]}},{"entity":"ClinVarVariant:40383","phenotype":{"types":[{"id":"HP:0000962","label":"Hyperkeratosis"}]}},{"entity":"ClinVarVariant:36073","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:49317","phenotype":{"types":[{"id":"HP:0009554","label":"Projection of scalp hair onto lateral cheek"}]}},{"entity":"MGI:1857166","phenotype":{"types":[{"id":"HP:0100494","label":"Abnormality of mast cells"}]}},{"entity":"ClinVarVariant:10725","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"ClinVarVariant:53706","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:68086","phenotype":{"types":[{"id":"HP:0000668","label":"Hypodontia"}]}},{"entity":"MGI:2684151","phenotype":{"types":[{"id":"MP:0000336","label":"decreased mast cell number"}]}},{"entity":"ClinVarVariant:13488","phenotype":{"types":[{"id":"HP:0000776","label":"Congenital diaphragmatic hernia"}]}},{"entity":"ClinVarVariant:42076","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:10987","phenotype":{"types":[{"id":"HP:0002181","label":"Cerebral edema"}]}},{"entity":"ClinVarVariant:7175","phenotype":{"types":[{"id":"HP:0001081","label":"Cholelithiasis"}]}},{"entity":"ClinVarVariant:53953","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:41469","phenotype":{"types":[{"id":"HP:0000239","label":"Large fontanelles"}]}},{"entity":"ClinVarVariant:135726","phenotype":{"types":[{"id":"HP:0007649","label":"Congenital hypertrophy of retinal pigment epithelium"}]}},{"entity":"ClinVarVariant:43595","phenotype":{"types":[{"id":"HP:0030078","label":"Lung adenocarcinoma"}]}},{"entity":"ClinVarVariant:16251","phenotype":{"types":[{"id":"HP:0000869","label":"Secondary amenorrhea"}]}},{"entity":"ClinVarVariant:102","phenotype":{"types":[{"id":"HP:0000987","label":"Atypical scarring of skin"}]}},{"entity":"ClinVarVariant:18054","phenotype":{"types":[{"id":"HP:0002961","label":"Dysgammaglobulinemia"}]}},{"entity":"MGI:2671578","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:136910","phenotype":{"types":[{"id":"HP:0005294","label":"Arterial dissection"}]}},{"entity":"ClinVarVariant:156049","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:216494","phenotype":{"types":[{"id":"HP:0001706","label":"Endocardial fibroelastosis"}]}},{"entity":"MGI:2183405","phenotype":{"types":[{"id":"MP:0009230","label":"abnormal sperm head morphology"}]}},{"entity":"ClinVarVariant:10877","phenotype":{"types":[{"id":"HP:0002872","label":"Apneic episodes precipitated by illness, fatigue, stress"}]}},{"entity":"MGI:1856054","phenotype":{"types":[{"id":"MP:0008892","label":"abnormal sperm flagellum morphology"}]}},{"entity":"ClinVarVariant:208832","phenotype":{"types":[{"id":"HP:0001199","label":"Triphalangeal thumb"}]}},{"entity":"ClinVarVariant:39036","phenotype":{"types":[{"id":"HP:0003026","label":"Short long bone"}]}},{"entity":"ClinVarVariant:68695","phenotype":{"types":[{"id":"HP:0001510","label":"Growth delay"}]}},{"entity":"ClinVarVariant:96338","phenotype":{"types":[{"id":"HP:0004523","label":"Long eyebrows"}]}},{"entity":"MGI:4458398","phenotype":{"types":[{"id":"HP:0005403","label":"T lymphocytopenia"}]}},{"entity":"ClinVarVariant:160087","phenotype":{"types":[{"id":"HP:0000280","label":"Coarse facial features"}]}},{"entity":"ClinVarVariant:262","phenotype":{"types":[{"id":"HP:0007759","label":"Opacification of the corneal stroma"}]}},{"entity":"dbSNP:rs41640954","phenotype":{"types":[{"id":"AQTLTrait:1169","label":"Interval to first estrus after calving"}]}},{"entity":"ClinVarVariant:211747","phenotype":{"types":[{"id":"HP:0000268","label":"Dolichocephaly"}]}},{"entity":"ClinVarVariant:53323","phenotype":{"types":[{"id":"HP:0100651","label":"Type I diabetes mellitus"}]}},{"entity":"ClinVarVariant:216220","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:30844","phenotype":{"types":[{"id":"HP:0010442","label":"Polydactyly"}]}},{"entity":"ClinVarVariant:190358","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"AQTL:162","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"AQTL:29894","phenotype":{"types":[{"id":"AQTLTrait:1081","label":"Age at puberty"}]}},{"entity":"ClinVarVariant:35703","phenotype":{"types":[{"id":"HP:0000934","label":"Chondrocalcinosis"}]}},{"entity":"ClinVarVariant:140986","phenotype":{"types":[{"id":"HP:0002035","label":"Rectal prolapse"}]}},{"entity":"ClinVarVariant:67916","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:189951","phenotype":{"types":[{"id":"HP:0005484","label":"Postnatal microcephaly"}]}},{"entity":"ClinVarVariant:41936","phenotype":{"types":[{"id":"HP:0002435","label":"Meningocele"}]}},{"entity":"AQTL:46123","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:180621","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"ClinVarVariant:216491","phenotype":{"types":[{"id":"HP:0000567","label":"Chorioretinal coloboma"}]}},{"entity":"ClinVarVariant:158375","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"AQTL:5581","phenotype":{"types":[{"id":"AQTLTrait:1181","label":"Muscle pH"}]}},{"entity":"ClinVarVariant:25006","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"ClinVarVariant:60706","phenotype":{"types":[{"id":"HP:0011904","label":"Persistence of hemoglobin F"}]}},{"entity":"ClinVarVariant:17254","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:159655","phenotype":{"types":[{"id":"HP:0000431","label":"Wide nasal bridge"}]}},{"entity":"ClinVarVariant:918","phenotype":{"types":[{"id":"HP:0002748","label":"Rickets"}]}},{"entity":"ClinVarVariant:1519","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:39504","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:11033","phenotype":{"types":[{"id":"HP:0001598","label":"Concave nail"}]}},{"entity":"ClinVarVariant:208834","phenotype":{"types":[{"id":"HP:0008678","label":"Renal hypoplasia/aplasia"}]}},{"entity":"ClinVarVariant:8371","phenotype":{"types":[{"id":"HP:0030325","label":"Cervicomedullary schisis"}]}},{"entity":"ClinVarVariant:21737","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"FlyBase:FBal0204417","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:210031","phenotype":{"types":[{"id":"HP:0000544","label":"External ophthalmoplegia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00016961-WBRNAi00091176","phenotype":{"types":[{"id":"WBPhenotype:0001422","label":"endocytic transport defect"}]}},{"entity":"ClinVarVariant:92727","phenotype":{"types":[{"id":"HP:0002912","label":"Methylmalonic acidemia"}]}},{"entity":"ClinVarVariant:53660","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:42393","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:209009","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"MGI:5548916","phenotype":{"types":[{"id":"MP:0003921","label":"abnormal heart left ventricle morphology"}]}},{"entity":"ClinVarVariant:13366","phenotype":{"types":[{"id":"HP:0001260","label":"Dysarthria"}]}},{"entity":"MGI:5294798","phenotype":{"types":[{"id":"MP:0011087","label":"neonatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:6678","phenotype":{"types":[{"id":"HP:0009025","label":"Increased connective tissue"}]}},{"entity":"MGI:2176538","phenotype":{"types":[{"id":"MP:0011098","label":"embryonic lethality during organogenesis, complete penetrance"}]}},{"entity":"ClinVarVariant:180631","phenotype":{"types":[{"id":"HP:0001433","label":"Hepatosplenomegaly"}]}},{"entity":"ClinVarVariant:4871","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"ClinVarVariant:189559","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-010724-5-ZDB-MRPHLNO-090818-5","phenotype":{"types":[{"id":"ZP:0000043","label":"abnormal(ly) decreased size eye"}]}},{"entity":"ClinVarVariant:186362","phenotype":{"types":[{"id":"HP:0000824","label":"Growth hormone deficiency"}]}},{"entity":"ClinVarVariant:37138","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"ClinVarVariant:10273","phenotype":{"types":[{"id":"HP:0005681","label":"Juvenile rheumatoid arthritis"}]}},{"entity":"ClinVarVariant:1035","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:65024","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:56203","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:8762","phenotype":{"types":[{"id":"HP:0008066","label":"Abnormal blistering of the skin"}]}},{"entity":"ZFIN:ZDB-ALT-070315-12","phenotype":{"types":[{"id":"ZP:0008827","label":"abnormal(ly) process quality branchiomeric skeletal muscle development"}]}},{"entity":"ClinVarVariant:6212","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:162385","phenotype":{"types":[{"id":"HP:0000998","label":"Hypertrichosis"}]}},{"entity":"dbSNP:rs41607431","phenotype":{"types":[{"id":"AQTLTrait:1115","label":"Chest width"}]}},{"entity":"ClinVarVariant:35706","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:54083","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:183262","phenotype":{"types":[{"id":"HP:0100689","label":"Decreased corneal thickness"}]}},{"entity":"ClinVarVariant:156109","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"MGI:3579250","phenotype":{"types":[{"id":"MP:0000229","label":"abnormal megakaryocyte differentiation"}]}},{"entity":"ClinVarVariant:83199","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"AQTL:40463","phenotype":{"types":[{"id":"AQTLTrait:1136","label":"Bone quality"}]}},{"entity":"WormBase:WBVar00252381","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:53600","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:93198","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"NCBIGene:474168","phenotype":{"types":[{"id":"HP:0000099","label":"Glomerulonephritis"}]}},{"entity":"ClinVarVariant:194859","phenotype":{"types":[{"id":"HP:0000256","label":"Macrocephaly"}]}},{"entity":"ClinVarVariant:30723","phenotype":{"types":[{"id":"HP:0007360","label":"Aplasia/Hypoplasia of the cerebellum"}]}},{"entity":"ClinVarVariant:25245","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:158580","phenotype":{"types":[{"id":"HP:0002002","label":"Deep philtrum"}]}},{"entity":"MGI:5444021","phenotype":{"types":[{"id":"MP:0001360","label":"abnormal social investigation"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-041212-76-ZDB-MRPHLNO-090513-3","phenotype":{"types":[{"id":"GO:0007368PHENOTYPE","label":"determination of left/right symmetry phenotype"}]}},{"entity":"ClinVarVariant:203516","phenotype":{"types":[{"id":"HP:0002841","label":"Recurrent fungal infections"}]}},{"entity":"ClinVarVariant:160035","phenotype":{"types":[{"id":"HP:0000430","label":"Underdeveloped nasal alae"}]}},{"entity":"ClinVarVariant:137952","phenotype":{"types":[{"id":"HP:0001841","label":"Preaxial foot polydactyly"}]}},{"entity":"ClinVarVariant:41170","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:49531","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:10128","phenotype":{"types":[{"id":"HP:0005542","label":"Prolonged whole-blood clotting time"}]}},{"entity":"ClinVarVariant:179061","phenotype":{"types":[{"id":"HP:0000691","label":"Microdontia"}]}},{"entity":"ClinVarVariant:136113","phenotype":{"types":[{"id":"HP:0000980","label":"Pallor"}]}},{"entity":"ClinVarVariant:198428","phenotype":{"types":[{"id":"HP:0004396","label":"Poor appetite"}]}},{"entity":"ClinVarVariant:92639","phenotype":{"types":[{"id":"HP:0100729","label":"Large face"}]}},{"entity":"ClinVarVariant:53923","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:16873","phenotype":{"types":[{"id":"HP:0002716","label":"Lymphadenopathy"}]}},{"entity":"ClinVarVariant:35866","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"ClinVarVariant:54000","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:53479","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:36062","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"MGI:1934269","phenotype":{"types":[{"id":"HP:0005506","label":"Chronic myelogenous leukemia"}]}},{"entity":"ClinVarVariant:31696","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:1720","phenotype":{"types":[{"id":"HP:0001511","label":"Intrauterine growth retardation"}]}},{"entity":"ClinVarVariant:3193","phenotype":{"types":[{"id":"HP:0008829","label":"Delayed femoral head ossification"}]}},{"entity":"MGI:5538688","phenotype":{"types":[{"id":"HP:0008734","label":"Decreased testicular size"}]}},{"entity":"ClinVarVariant:56181","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:66051","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:16327","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"ClinVarVariant:75243","phenotype":{"types":[{"id":"HP:0100034","label":"Motor tics"}]}},{"entity":"MGI:2679499","phenotype":{"types":[{"id":"GO:0009887PHENOTYPE","label":"organ morphogenesis phenotype"}]}},{"entity":"ClinVarVariant:31210","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:13045","phenotype":{"types":[{"id":"HP:0001123","label":"Visual field defect"}]}},{"entity":"ClinVarVariant:179632","phenotype":{"types":[{"id":"HP:0004937","label":"Pulmonary artery aneurysm"}]}},{"entity":"ClinVarVariant:1866","phenotype":{"types":[{"id":"HP:0002315","label":"Headache"}]}},{"entity":"ClinVarVariant:29652","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ZFIN:ZDB-ALT-980203-386","phenotype":{"types":[{"id":"ZP:0000528","label":"abnormal(ly) decreased size cardiac ventricle"}]}},{"entity":"ClinVarVariant:204218","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:211647","phenotype":{"types":[{"id":"HP:0000776","label":"Congenital diaphragmatic hernia"}]}},{"entity":"ClinVarVariant:67368","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001500-WBRNAi00038528","phenotype":{"types":[{"id":"WBPhenotype:0002046","label":"iron homeostasis variant"}]}},{"entity":"ClinVarVariant:49541","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"MGI:3697906","phenotype":{"types":[{"id":"HP:0000234","label":"Abnormality of the head"}]}},{"entity":"ClinVarVariant:198399","phenotype":{"types":[{"id":"HP:0001279","label":"Syncope"}]}},{"entity":"FlyBase:FBal0294194","phenotype":{"types":[{"id":"FBbt:00004133PHENOTYPE","label":"interommatidial bristle phenotype"}]}},{"entity":"ClinVarVariant:95419","phenotype":{"types":[{"id":"HP:0003487","label":"Babinski sign"}]}},{"entity":"ClinVarVariant:1331","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"ClinVarVariant:162400","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"ClinVarVariant:120300","phenotype":{"types":[{"id":"HP:0002071","label":"Abnormality of extrapyramidal motor function"}]}},{"entity":"ClinVarVariant:7315","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"ClinVarVariant:65617","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"MGI:4356015","phenotype":{"types":[{"id":"MP:0005222","label":"abnormal somite size"}]}},{"entity":"ClinVarVariant:24990","phenotype":{"types":[{"id":"HP:0200042","label":"Skin ulcer"}]}},{"entity":"ClinVarVariant:53350","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:1010","phenotype":{"types":[{"id":"HP:0000512","label":"Abnormal electroretinogram"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001186-WBRNAi00086860","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:92545","phenotype":{"types":[{"id":"HP:0002326","label":"Transient ischemic attack"}]}},{"entity":"ClinVarVariant:38726","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:191776","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"FlyBase:FBal0031399","phenotype":{"types":[{"id":"FBbt:00004233PHENOTYPE","label":"Drosophila tertiary pigment cell phenotype"}]}},{"entity":"ClinVarVariant:188299","phenotype":{"types":[{"id":"HP:0010610","label":"Palmar pits"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00044585-WBRNAi00024788","phenotype":{"types":[{"id":"WBPhenotype:0000643","label":"locomotion variant"}]}},{"entity":"ClinVarVariant:42130","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:49521","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"MGI:2137552","phenotype":{"types":[{"id":"MP:0003935","label":"abnormal craniofacial development"}]}},{"entity":"ClinVarVariant:38629","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"ClinVarVariant:143768","phenotype":{"types":[{"id":"HP:0000478","label":"Abnormality of the eye"}]}},{"entity":"ClinVarVariant:24826","phenotype":{"types":[{"id":"HP:0001636","label":"Tetralogy of Fallot"}]}},{"entity":"ClinVarVariant:850","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019835-WBRNAi00082433","phenotype":{"types":[{"id":"WBPhenotype:0001037","label":"sterile progeny"}]}},{"entity":"ClinVarVariant:7185","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:17284","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:24656","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"FlyBase:FBal0276873","phenotype":{"types":[{"id":"FBbt:00004508PHENOTYPE","label":"eye phenotype"}]}},{"entity":"AQTL:24787","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:11850","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"MGI:5297423","phenotype":{"types":[{"id":"HP:0001719","label":"Double outlet right ventricle"}]}},{"entity":"ClinVarVariant:12041","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:53725","phenotype":{"types":[{"id":"HP:0004936","label":"Venous thrombosis"}]}},{"entity":"ClinVarVariant:42355","phenotype":{"types":[{"id":"HP:0004933","label":"Ascending aortic dissection"}]}},{"entity":"ClinVarVariant:24265","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"ClinVarVariant:2264","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"MGI:1857632","phenotype":{"types":[{"id":"MP:0004342","label":"scapular bone foramen"}]}},{"entity":"MGI:3526866","phenotype":{"types":[{"id":"MP:0000157","label":"abnormal sternum morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00009498-WBRNAi00085795","phenotype":{"types":[{"id":"WBPhenotype:0001952","label":"germline nuclear positioning variant"}]}},{"entity":"ClinVarVariant:4135","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"ClinVarVariant:54063","phenotype":{"types":[{"id":"HP:0000966","label":"Hypohidrosis"}]}},{"entity":"ClinVarVariant:159076","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:192290","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"ClinVarVariant:167144","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:143120","phenotype":{"types":[{"id":"HP:0000622","label":"Blurred vision"}]}},{"entity":"FlyBase:FBal0294983","phenotype":{"types":[{"id":"FBcv:0000385","label":"short lived"}]}},{"entity":"ClinVarVariant:42317","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"ClinVarVariant:53732","phenotype":{"types":[{"id":"HP:0011947","label":"Respiratory tract infection"}]}},{"entity":"ClinVarVariant:11668","phenotype":{"types":[{"id":"HP:0000498","label":"Blepharitis"}]}},{"entity":"ClinVarVariant:30851","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:13153","phenotype":{"types":[{"id":"HP:0001874","label":"Abnormality of neutrophils"}]}},{"entity":"ClinVarVariant:101354","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"MGI:5522949","phenotype":{"types":[{"id":"MP:0002662","label":"abnormal cauda epididymis morphology"}]}},{"entity":"ClinVarVariant:30182","phenotype":{"types":[{"id":"HP:0003312","label":"Abnormal form of the vertebral bodies"}]}},{"entity":"ClinVarVariant:11114","phenotype":{"types":[{"id":"HP:0001891","label":"Iron deficiency anemia"}]}},{"entity":"ClinVarVariant:10735","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"FlyBase:FBal0095354","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:41334","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:5424","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"ClinVarVariant:12981","phenotype":{"types":[{"id":"HP:0003324","label":"Generalized muscle weakness"}]}},{"entity":"ClinVarVariant:216845","phenotype":{"types":[{"id":"HP:0001663","label":"Ventricular fibrillation"}]}},{"entity":"ClinVarVariant:142378","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:163768","phenotype":{"types":[{"id":"HP:0000766","label":"Abnormality of the sternum"}]}},{"entity":"ClinVarVariant:40069","phenotype":{"types":[{"id":"HP:0000110","label":"Renal dysplasia"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-060503-240-ZDB-MRPHLNO-101202-1","phenotype":{"types":[{"id":"ZP:0003746","label":"abnormal(ly) delayed angiogenesis"}]}},{"entity":"ClinVarVariant:195329","phenotype":{"types":[{"id":"HP:0000368","label":"Low-set, posteriorly rotated ears"}]}},{"entity":"ClinVarVariant:40249","phenotype":{"types":[{"id":"HP:0100704","label":"Cortical visual impairment"}]}},{"entity":"ClinVarVariant:95454","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:41252","phenotype":{"types":[{"id":"HP:0010298","label":"Smooth tongue"}]}},{"entity":"dbSNP:rs41571256","phenotype":{"types":[{"id":"AQTLTrait:1070","label":"Inseminations per conception"}]}},{"entity":"ClinVarVariant:210016","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:42382","phenotype":{"types":[{"id":"HP:0001380","label":"Ligamentous laxity"}]}},{"entity":"MGI:3530566","phenotype":{"types":[{"id":"HP:0000135","label":"Hypogonadism"}]}},{"entity":"ClinVarVariant:40452","phenotype":{"types":[{"id":"HP:0003510","label":"Severe short stature"}]}},{"entity":"ClinVarVariant:17294","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:36530","phenotype":{"types":[{"id":"HP:0003072","label":"Hypercalcemia"}]}},{"entity":"ClinVarVariant:216568","phenotype":{"types":[{"id":"HP:0002665","label":"Lymphoma"}]}},{"entity":"ClinVarVariant:38909","phenotype":{"types":[{"id":"HP:0003521","label":"Disproportionate short-trunk short stature"}]}},{"entity":"_:genid1939651","phenotype":{"types":[{"id":"ZP:0000335","label":"abnormal(ly) disrupted blood circulation"}]}},{"entity":"ClinVarVariant:42333","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"ClinVarVariant:101286","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:100762","phenotype":{"types":[{"id":"HP:0000174","label":"Abnormality of the palate"}]}},{"entity":"ClinVarVariant:10997","phenotype":{"types":[{"id":"HP:0002181","label":"Cerebral edema"}]}},{"entity":"ClinVarVariant:91680","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:211317","phenotype":{"types":[{"id":"HP:0003312","label":"Abnormal form of the vertebral bodies"}]}},{"entity":"ClinVarVariant:25103","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:159952","phenotype":{"types":[{"id":"HP:0100627","label":"Displacement of the external urethral meatus"}]}},{"entity":"_:genid1976450","phenotype":{"types":[{"id":"ZP:0000038","label":"abnormal(ly) edematous pericardium"}]}},{"entity":"ClinVarVariant:10745","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"dbSNP:rs7756992","phenotype":{"types":[{"id":"HP:0002155","label":"Hypertriglyceridemia"}]}},{"entity":"ClinVarVariant:24583","phenotype":{"types":[{"id":"HP:0010784","label":"Uterine neoplasm"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007008-WBRNAi00064202","phenotype":{"types":[{"id":"WBPhenotype:0000730","label":"apoptosis variant"}]}},{"entity":"ClinVarVariant:9589","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:12788","phenotype":{"types":[{"id":"HP:0011976","label":"Elevated urinary catecholamines"}]}},{"entity":"ClinVarVariant:216729","phenotype":{"types":[{"id":"HP:0100634","label":"Neuroendocrine neoplasm"}]}},{"entity":"MGI:2446069","phenotype":{"types":[{"id":"MP:0008395","label":"abnormal osteoblast differentiation"}]}},{"entity":"ClinVarVariant:14356","phenotype":{"types":[{"id":"HP:0007657","label":"Diffuse nuclear cataract"}]}},{"entity":"ClinVarVariant:7834","phenotype":{"types":[{"id":"HP:0004481","label":"Progressive macrocephaly"}]}},{"entity":"ClinVarVariant:210404","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"WormBase:WBVar00145377","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:16275","phenotype":{"types":[{"id":"HP:0002667","label":"Nephroblastoma (Wilms tumor)"}]}},{"entity":"ClinVarVariant:158319","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:42114","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:210436","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"ClinVarVariant:39026","phenotype":{"types":[{"id":"HP:0003026","label":"Short long bone"}]}},{"entity":"MGI:1856392","phenotype":{"types":[{"id":"HP:0007544","label":"Piebaldism"}]}},{"entity":"dbSNP:rs29010222","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:53535","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000817-WBRNAi00086749","phenotype":{"types":[{"id":"WBPhenotype:0001036","label":"sterile F1"}]}},{"entity":"ClinVarVariant:143264","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"ClinVarVariant:53943","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:53493","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:159024","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"ClinVarVariant:215698","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:55951","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:60536","phenotype":{"types":[{"id":"HP:0002172","label":"Postural instability"}]}},{"entity":"ClinVarVariant:48816","phenotype":{"types":[{"id":"HP:0009720","label":"Adenoma sebaceum"}]}},{"entity":"MGI:3774018","phenotype":{"types":[{"id":"MP:0011087","label":"neonatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:49510","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:56213","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:156160","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"MGI:5646298","phenotype":{"types":[{"id":"HP:0002180","label":"Neurodegeneration"}]}},{"entity":"ClinVarVariant:21525","phenotype":{"types":[{"id":"HP:0001256","label":"Intellectual disability, mild"}]}},{"entity":"ClinVarVariant:4311","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"AQTL:5929","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"FlyBase:FBal0269430","phenotype":{"types":[{"id":"FBbt:00002743PHENOTYPE","label":"Drosophila T1 beard phenotype"}]}},{"entity":"ClinVarVariant:31675","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"ClinVarVariant:49257","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"NCBIGene:100188011","phenotype":{"types":[{"id":"HP:0002789","label":"Tachypnea"}]}},{"entity":"ClinVarVariant:136120","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:2722","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"FlyBase:FBal0124416","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:156720","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"WormBase:WBVar00248887","phenotype":{"types":[{"id":"WBPhenotype:0000698","label":"vulvaless"}]}},{"entity":"ClinVarVariant:40706","phenotype":{"types":[{"id":"HP:0000027","label":"Azoospermia"}]}},{"entity":"ClinVarVariant:13836","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:56096","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"ClinVarVariant:41513","phenotype":{"types":[{"id":"HP:0002895","label":"Papillary thyroid carcinoma"}]}},{"entity":"ClinVarVariant:17374","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:40493","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:49571","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"NCBIGene:46","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"ClinVarVariant:9303","phenotype":{"types":[{"id":"HP:0000340","label":"Sloping forehead"}]}},{"entity":"ClinVarVariant:3853","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:133101","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:53206","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"dbSNP:rs41937398","phenotype":{"types":[{"id":"AQTLTrait:1101","label":"Foot angle"}]}},{"entity":"ClinVarVariant:10275","phenotype":{"types":[{"id":"HP:0001369","label":"Arthritis"}]}},{"entity":"ClinVarVariant:54004","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:15326","phenotype":{"types":[{"id":"HP:0011031","label":"Abnormality of iron homeostasis"}]}},{"entity":"ClinVarVariant:92555","phenotype":{"types":[{"id":"HP:0002326","label":"Transient ischemic attack"}]}},{"entity":"ClinVarVariant:49551","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:94537","phenotype":{"types":[{"id":"HP:0006466","label":"Ankle contracture"}]}},{"entity":"ClinVarVariant:143160","phenotype":{"types":[{"id":"HP:0003474","label":"Sensory impairment"}]}},{"entity":"ClinVarVariant:135685","phenotype":{"types":[{"id":"HP:0008069","label":"Neoplasm of the skin"}]}},{"entity":"ClinVarVariant:2251","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:1525","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:50993","phenotype":{"types":[{"id":"HP:0009882","label":"Short distal phalanx of finger"}]}},{"entity":"MGI:2678815","phenotype":{"types":[{"id":"MP:0001212","label":"skin lesions"}]}},{"entity":"ClinVarVariant:7155","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001924-WBRNAi00068386","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:92747","phenotype":{"types":[{"id":"HP:0002912","label":"Methylmalonic acidemia"}]}},{"entity":"ClinVarVariant:30040","phenotype":{"types":[{"id":"HP:0000311","label":"Round face"}]}},{"entity":"ClinVarVariant:180277","phenotype":{"types":[{"id":"HP:0001084","label":"Corneal arcus"}]}},{"entity":"ClinVarVariant:36438","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:38950","phenotype":{"types":[{"id":"HP:0001876","label":"Pancytopenia"}]}},{"entity":"ClinVarVariant:93752","phenotype":{"types":[{"id":"HP:0000668","label":"Hypodontia"}]}},{"entity":"ClinVarVariant:14184","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"MGI:4840274","phenotype":{"types":[{"id":"MP:0008185","label":"decreased naive B cell number"}]}},{"entity":"MGI:1857225","phenotype":{"types":[{"id":"MP:0008189","label":"increased transitional stage B cell number"}]}},{"entity":"ClinVarVariant:215688","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:30293","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:4354","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"ClinVarVariant:50061","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:94691","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:189113","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:53297","phenotype":{"types":[{"id":"HP:0001648","label":"Cor pulmonale"}]}},{"entity":"MGI:5463664","phenotype":{"types":[{"id":"HP:0002910","label":"Elevated hepatic transaminases"}]}},{"entity":"ClinVarVariant:188272","phenotype":{"types":[{"id":"HP:0000892","label":"Bifid ribs"}]}},{"entity":"ClinVarVariant:65895","phenotype":{"types":[{"id":"HP:0001392","label":"Abnormality of the liver"}]}},{"entity":"ClinVarVariant:53356","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004010-WBRNAi00063019","phenotype":{"types":[{"id":"WBPhenotype:0000709","label":"pharyngeal morphology variant"}]}},{"entity":"ClinVarVariant:167303","phenotype":{"types":[{"id":"HP:0008368","label":"Tarsal synostosis"}]}},{"entity":"ClinVarVariant:132708","phenotype":{"types":[{"id":"HP:0009919","label":"Retinoblastoma"}]}},{"entity":"ClinVarVariant:36314","phenotype":{"types":[{"id":"HP:0002835","label":"Aspiration"}]}},{"entity":"MGI:1858064","phenotype":{"types":[{"id":"GO:0043473PHENOTYPE","label":"pigmentation phenotype"}]}},{"entity":"ClinVarVariant:49462","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:53481","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:9008","phenotype":{"types":[{"id":"HP:0004383","label":"Hypoplastic left heart"}]}},{"entity":"ClinVarVariant:210444","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ZFIN:ZDB-ALT-040726-6","phenotype":{"types":[{"id":"ZP:0002272","label":"abnormal(ly) necrotic brain"}]}},{"entity":"ClinVarVariant:13693","phenotype":{"types":[{"id":"HP:0001082","label":"Cholecystitis"}]}},{"entity":"ClinVarVariant:133328","phenotype":{"types":[{"id":"HP:0012448","label":"Delayed myelination"}]}},{"entity":"FlyBase:FBal0058766","phenotype":{"types":[{"id":"FBcv:0000386","label":"long lived"}]}},{"entity":"ClinVarVariant:65285","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"MGI:4412094","phenotype":{"types":[{"id":"MP:0000260","label":"abnormal angiogenesis"}]}},{"entity":"ClinVarVariant:66461","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"ClinVarVariant:65104","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:2036","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:4330","phenotype":{"types":[{"id":"HP:0003540","label":"Impaired platelet aggregation"}]}},{"entity":"ClinVarVariant:36092","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"AQTL:15021","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:53931","phenotype":{"types":[{"id":"HP:0003453","label":"Antineutrophil antibody positivity"}]}},{"entity":"ClinVarVariant:210006","phenotype":{"types":[{"id":"HP:0002140","label":"Ischemic stroke"}]}},{"entity":"dbSNP:rs110432080","phenotype":{"types":[{"id":"AQTLTrait:1253","label":"Milk stearic acid percentage"}]}},{"entity":"ClinVarVariant:53690","phenotype":{"types":[{"id":"HP:0011947","label":"Respiratory tract infection"}]}},{"entity":"ClinVarVariant:2568","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:136042","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:9723","phenotype":{"types":[{"id":"HP:0002083","label":"Migraine without aura"}]}},{"entity":"FlyBase:FBal0207483","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:133175","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:68701","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:10144","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:101122","phenotype":{"types":[{"id":"HP:0000490","label":"Deeply set eye"}]}},{"entity":"MGI:3054057","phenotype":{"types":[{"id":"HP:0003110","label":"Abnormality of urine homeostasis"}]}},{"entity":"NCBIGene:100188278","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:38317","phenotype":{"types":[{"id":"HP:0000089","label":"Renal hypoplasia"}]}},{"entity":"ClinVarVariant:2139","phenotype":{"types":[{"id":"HP:0002036","label":"Hiatus hernia"}]}},{"entity":"ClinVarVariant:143572","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:215586","phenotype":{"types":[{"id":"HP:0005550","label":"Chronic lymphatic leukemia"}]}},{"entity":"ClinVarVariant:100930","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:53953","phenotype":{"types":[{"id":"HP:0011950","label":"Bronchiolitis"}]}},{"entity":"ClinVarVariant:82650","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"WormBase:WBVar00242504","phenotype":{"types":[{"id":"WBPhenotype:0000012","label":"dauer constitutive"}]}},{"entity":"ClinVarVariant:65311","phenotype":{"types":[{"id":"HP:0003764","label":"Nevus"}]}},{"entity":"ClinVarVariant:158661","phenotype":{"types":[{"id":"HP:0009937","label":"Facial hirsutism"}]}},{"entity":"ClinVarVariant:30293","phenotype":{"types":[{"id":"HP:0000632","label":"Lacrimation abnormality"}]}},{"entity":"dbSNP:rs109839918","phenotype":{"types":[{"id":"AQTLTrait:1096","label":"Teat length"}]}},{"entity":"ClinVarVariant:39868","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:10014","phenotype":{"types":[{"id":"HP:0030344","label":"Decreased circulating luteinizing hormone level"}]}},{"entity":"ClinVarVariant:145","phenotype":{"types":[{"id":"HP:0001308","label":"Tongue fasciculations"}]}},{"entity":"ClinVarVariant:10692","phenotype":{"types":[{"id":"HP:0100639","label":"Erectile abnormalities"}]}},{"entity":"ClinVarVariant:36096","phenotype":{"types":[{"id":"HP:0001002","label":"Decreased subcutaneous fat"}]}},{"entity":"ClinVarVariant:8643","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"FlyBase:FBal0207769","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017546-WBRNAi00099316","phenotype":{"types":[{"id":"WBPhenotype:0000961","label":"pattern of transgene expression variant"}]}},{"entity":"ClinVarVariant:30964","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001972-WBRNAi00068412","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:143515","phenotype":{"types":[{"id":"HP:0000729","label":"Autistic behavior"}]}},{"entity":"ClinVarVariant:54014","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:45003","phenotype":{"types":[{"id":"HP:0011034","label":"Amyloidosis"}]}},{"entity":"MGI:5286584","phenotype":{"types":[{"id":"HP:0002446","label":"Astrocytosis"}]}},{"entity":"ClinVarVariant:43601","phenotype":{"types":[{"id":"HP:0009726","label":"Renal neoplasm"}]}},{"entity":"OMIM:220210","phenotype":{"types":[{"id":"HP:0010935","label":"Abnormality of the upper urinary tract"}]}},{"entity":"ClinVarVariant:210485","phenotype":{"types":[{"id":"HP:0007327","label":"Mixed demyelinating and axonal polyneuropathy"}]}},{"entity":"ClinVarVariant:36754","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"ClinVarVariant:67997","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"dbSNP:rs1819084","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:12604","phenotype":{"types":[{"id":"HP:0001067","label":"Neurofibromas"}]}},{"entity":"ClinVarVariant:156003","phenotype":{"types":[{"id":"HP:0100533","label":"Inflammatory abnormality of the eye"}]}},{"entity":"ClinVarVariant:25300","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:92575","phenotype":{"types":[{"id":"HP:0002326","label":"Transient ischemic attack"}]}},{"entity":"ClinVarVariant:66481","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"ClinVarVariant:50259","phenotype":{"types":[{"id":"HP:0005897","label":"Severe generalized osteoporosis"}]}},{"entity":"ClinVarVariant:53876","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:208009","phenotype":{"types":[{"id":"HP:0001482","label":"Subcutaneous nodule"}]}},{"entity":"FlyBase:FBal0239575","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004815-WBRNAi00086787","phenotype":{"types":[{"id":"WBPhenotype:0000793","label":"posterior body morphology variant"}]}},{"entity":"ClinVarVariant:101152","phenotype":{"types":[{"id":"HP:0010318","label":"Aplasia/Hypoplasia of the abdominal wall musculature"}]}},{"entity":"ClinVarVariant:97040","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"ClinVarVariant:6794","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"dbSNP:rs41859871","phenotype":{"types":[{"id":"AQTLTrait:1292","label":"Early embryonic survival"}]}},{"entity":"ClinVarVariant:10755","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"ClinVarVariant:10609","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:159081","phenotype":{"types":[{"id":"HP:0000752","label":"Hyperactivity"}]}},{"entity":"ClinVarVariant:9973","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:102433","phenotype":{"types":[{"id":"HP:0003128","label":"Lactic acidosis"}]}},{"entity":"MGI:2176174","phenotype":{"types":[{"id":"MP:0011028","label":"impaired branching involved in bronchus morphogenesis"}]}},{"entity":"ClinVarVariant:64987","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"dbSNP:rs4793501","phenotype":{"types":[{"id":"HP:0000539","label":"Abnormality of refraction"}]}},{"entity":"ClinVarVariant:18337","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:36520","phenotype":{"types":[{"id":"HP:0003072","label":"Hypercalcemia"}]}},{"entity":"ClinVarVariant:91670","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"AQTL:10280","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:204086","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"_:genid1972511","phenotype":{"types":[{"id":"ZP:0002787","label":"abnormal(ly) decreased size intestinal epithelium"}]}},{"entity":"FlyBase:FBal0047091","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"MGI:4941848","phenotype":{"types":[{"id":"MP:0003956","label":"abnormal body size"}]}},{"entity":"ClinVarVariant:36381","phenotype":{"types":[{"id":"HP:0001597","label":"Abnormality of the nail"}]}},{"entity":"ClinVarVariant:53524","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"ClinVarVariant:177959","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:53340","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:1379","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:9877","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:7188","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:2149","phenotype":{"types":[{"id":"HP:0002036","label":"Hiatus hernia"}]}},{"entity":"dbSNP:rs11986414","phenotype":{"types":[{"id":"HP:0001433","label":"Hepatosplenomegaly"}]}},{"entity":"ClinVarVariant:13335","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:9946","phenotype":{"types":[{"id":"HP:0001923","label":"Reticulocytosis"}]}},{"entity":"ClinVarVariant:10239","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:3042795","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:90871","phenotype":{"types":[{"id":"HP:0100574","label":"Biliary tract neoplasm"}]}},{"entity":"WormBase:WBVar00146684","phenotype":{"types":[{"id":"WBPhenotype:0001846","label":"phagosome maturation defective"}]}},{"entity":"ClinVarVariant:216715","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006994-WBRNAi00088835","phenotype":{"types":[{"id":"WBPhenotype:0001588","label":"microtubule organization biogenesis variant"}]}},{"entity":"ClinVarVariant:91320","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:65118","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:208580","phenotype":{"types":[{"id":"HP:0002414","label":"Spina bifida"}]}},{"entity":"ClinVarVariant:9733","phenotype":{"types":[{"id":"HP:0002083","label":"Migraine without aura"}]}},{"entity":"ClinVarVariant:141815","phenotype":{"types":[{"id":"HP:0002017","label":"Nausea and vomiting"}]}},{"entity":"ClinVarVariant:24826","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ClinVarVariant:41655","phenotype":{"types":[{"id":"HP:0100730","label":"Bronchogenic cyst"}]}},{"entity":"ClinVarVariant:24361","phenotype":{"types":[{"id":"HP:0200020","label":"Corneal erosion"}]}},{"entity":"FlyBase:FBal0314224","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:2261","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:10335","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:30910","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"ClinVarVariant:53636","phenotype":{"types":[{"id":"HP:0006510","label":"Chronic obstructive pulmonary disease"}]}},{"entity":"ClinVarVariant:44804","phenotype":{"types":[{"id":"HP:0000368","label":"Low-set, posteriorly rotated ears"}]}},{"entity":"ClinVarVariant:36071","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:2199","phenotype":{"types":[{"id":"HP:0000408","label":"Progressive sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:11934","phenotype":{"types":[{"id":"HP:0002315","label":"Headache"}]}},{"entity":"ClinVarVariant:53728","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:21555","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019126-WBRNAi00091874","phenotype":{"types":[{"id":"WBPhenotype:0001372","label":"protein DNA interaction variant"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001177-WBRNAi00088701","phenotype":{"types":[{"id":"WBPhenotype:0002059","label":"pore forming toxin hypersensitive"}]}},{"entity":"ClinVarVariant:53284","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000866-WBRNAi00007858","phenotype":{"types":[{"id":"WBPhenotype:0001083","label":"multiple cytoplasmic cavities early emb"}]}},{"entity":"FlyBase:FBal0278276","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:95624","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:819","phenotype":{"types":[{"id":"HP:0200040","label":"Epidermoid cyst"}]}},{"entity":"ClinVarVariant:38806","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"AQTL:49870","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:5142","phenotype":{"types":[{"id":"HP:0000144","label":"Decreased fertility"}]}},{"entity":"ClinVarVariant:53188","phenotype":{"types":[{"id":"HP:0004395","label":"Malnutrition"}]}},{"entity":"ClinVarVariant:194962","phenotype":{"types":[{"id":"HP:0001608","label":"Abnormality of the voice"}]}},{"entity":"ClinVarVariant:159224","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:101105","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"AQTL:11222","phenotype":{"types":[{"id":"AQTLTrait:1027","label":"Marbling score"}]}},{"entity":"ClinVarVariant:64789","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"WormBase:WBVar00250996","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:49591","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"FlyBase:FBal0209601","phenotype":{"types":[{"id":"FBcv:0000385","label":"short lived"}]}},{"entity":"MGI:2678247","phenotype":{"types":[{"id":"MP:0004768","label":"abnormal axonal transport"}]}},{"entity":"ClinVarVariant:30231","phenotype":{"types":[{"id":"HP:0000527","label":"Long eyelashes"}]}},{"entity":"ClinVarVariant:136202","phenotype":{"types":[{"id":"HP:0000750","label":"Delayed speech and language development"}]}},{"entity":"MGI:5620941","phenotype":{"types":[{"id":"MP:0003098","label":"decreased tendon stiffness"}]}},{"entity":"ClinVarVariant:9818","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:38486","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"ClinVarVariant:210414","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:10727","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"ClinVarVariant:49581","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:16209","phenotype":{"types":[{"id":"HP:0010819","label":"Atonic seizures"}]}},{"entity":"ClinVarVariant:7199","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:36791","phenotype":{"types":[{"id":"HP:0006335","label":"Persistence of primary teeth"}]}},{"entity":"MGI:2429699","phenotype":{"types":[{"id":"HP:0012373","label":"Abnormal eye physiology"}]}},{"entity":"AQTL:16489","phenotype":{"types":[{"id":"AQTLTrait:1173","label":"Rear leg set"}]}},{"entity":"ClinVarVariant:41523","phenotype":{"types":[{"id":"HP:0002895","label":"Papillary thyroid carcinoma"}]}},{"entity":"ClinVarVariant:159218","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"ClinVarVariant:158734","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"ClinVarVariant:156221","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"ClinVarVariant:53913","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:141514","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"MGI:4364926","phenotype":{"types":[{"id":"HP:0011877","label":"Increased mean platelet volume"}]}},{"entity":"MGI:1856226","phenotype":{"types":[{"id":"MP:0001265","label":"decreased body size"}]}},{"entity":"ClinVarVariant:159380","phenotype":{"types":[{"id":"HP:0009890","label":"High anterior hairline"}]}},{"entity":"ClinVarVariant:160081","phenotype":{"types":[{"id":"HP:0001298","label":"Encephalopathy"}]}},{"entity":"FlyBase:FBal0210535","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:127501","phenotype":{"types":[{"id":"HP:0000268","label":"Dolichocephaly"}]}},{"entity":"FlyBase:FBal0242677","phenotype":{"types":[{"id":"FBbt:00002027PHENOTYPE","label":"Drosophila dorsal multidendritic neuron ddaC phenotype"}]}},{"entity":"ClinVarVariant:5539","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"ClinVarVariant:88731","phenotype":{"types":[{"id":"HP:0002307","label":"Drooling"}]}},{"entity":"FlyBase:FBal0230781","phenotype":{"types":[{"id":"FBcv:0002027","label":"lethal - all die before end of pupal stage"}]}},{"entity":"ClinVarVariant:197858","phenotype":{"types":[{"id":"HP:0003300","label":"Ovoid vertebral bodies"}]}},{"entity":"FlyBase:FBal0137561","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:120310","phenotype":{"types":[{"id":"HP:0002071","label":"Abnormality of extrapyramidal motor function"}]}},{"entity":"ClinVarVariant:210018","phenotype":{"types":[{"id":"HP:0009113","label":"Diaphragmatic weakness"}]}},{"entity":"ClinVarVariant:25297","phenotype":{"types":[{"id":"HP:0008209","label":"Premature ovarian failure"}]}},{"entity":"MGI:5527244","phenotype":{"types":[{"id":"HP:0100522","label":"Thymoma"}]}},{"entity":"ClinVarVariant:53175","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"ClinVarVariant:2365","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:4142","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:6915","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:53881","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:94530","phenotype":{"types":[{"id":"HP:0100578","label":"Lipoatrophy"}]}},{"entity":"ClinVarVariant:215763","phenotype":{"types":[{"id":"HP:0100242","label":"Sarcoma"}]}},{"entity":"ClinVarVariant:222","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:10741","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:1113","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:67871","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"MGI:1931047","phenotype":{"types":[{"id":"MP:0010572","label":"persistent right dorsal aorta"}]}},{"entity":"ClinVarVariant:48708","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:30249","phenotype":{"types":[{"id":"HP:0000046","label":"Scrotal hypoplasia"}]}},{"entity":"ClinVarVariant:128250","phenotype":{"types":[{"id":"HP:0002490","label":"Increased CSF lactate"}]}},{"entity":"ClinVarVariant:41075","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"WormBase:WBVar00142906","phenotype":{"types":[{"id":"WBPhenotype:0001516","label":"helical cuticle"}]}},{"entity":"MGI:3837468","phenotype":{"types":[{"id":"HP:0004324","label":"Increased body weight"}]}},{"entity":"WormBase:WBVar00143933","phenotype":{"types":[{"id":"WBPhenotype:0000905","label":"neuron morphology variant"}]}},{"entity":"ClinVarVariant:10078","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"MGI:4442818","phenotype":{"types":[{"id":"MP:0000358","label":"abnormal cell morphology"}]}},{"entity":"MGI:2388594","phenotype":{"types":[{"id":"MP:0006288","label":"small otic capsule"}]}},{"entity":"ClinVarVariant:13172","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:2814","phenotype":{"types":[{"id":"HP:0002435","label":"Meningocele"}]}},{"entity":"ClinVarVariant:49939","phenotype":{"types":[{"id":"HP:0009719","label":"Hypomelanotic macule"}]}},{"entity":"ClinVarVariant:101372","phenotype":{"types":[{"id":"HP:0006323","label":"Premature loss of primary teeth"}]}},{"entity":"ZFIN:ZDB-ALT-121112-2","phenotype":{"types":[{"id":"ZP:0017910","label":"abnormal(ly) disrupted amino-acid betaine transport"}]}},{"entity":"ClinVarVariant:215774","phenotype":{"types":[{"id":"HP:0010743","label":"Short metatarsal"}]}},{"entity":"ClinVarVariant:13713","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:24452","phenotype":{"types":[{"id":"HP:0008619","label":"Bilateral sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:5424","phenotype":{"types":[{"id":"HP:0005222","label":"Bowel diverticulosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001398-WBRNAi00027267","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"MGI:3698412","phenotype":{"types":[{"id":"MP:0008713","label":"abnormal cytokine level"}]}},{"entity":"ClinVarVariant:10706","phenotype":{"types":[{"id":"HP:0002023","label":"Anal atresia"}]}},{"entity":"ClinVarVariant:24666","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"ClinVarVariant:181711","phenotype":{"types":[{"id":"HP:0009765","label":"Low hanging columella"}]}},{"entity":"AQTL:48427","phenotype":{"types":[{"id":"AQTLTrait:1067","label":"Length of productive life"}]}},{"entity":"ClinVarVariant:101259","phenotype":{"types":[{"id":"HP:0000015","label":"Bladder diverticulum"}]}},{"entity":"ClinVarVariant:94681","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"FlyBase:FBal0137126","phenotype":{"types":[{"id":"FBbt:00005200PHENOTYPE","label":"denticle phenotype"}]}},{"entity":"ClinVarVariant:25340","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"ClinVarVariant:6066","phenotype":{"types":[{"id":"HP:0009777","label":"Absent thumb"}]}},{"entity":"ClinVarVariant:54024","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1303","phenotype":{"types":[{"id":"ZP:0000719","label":"abnormal(ly) non-contractile heart"}]}},{"entity":"ClinVarVariant:185817","phenotype":{"types":[{"id":"HP:0002076","label":"Migraine"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1164","phenotype":{"types":[{"id":"ZP:0005400","label":"abnormal(ly) hypoplastic horizontal myoseptum"}]}},{"entity":"ClinVarVariant:30939","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"ClinVarVariant:159249","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:53933","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:67868","phenotype":{"types":[{"id":"HP:0004756","label":"Ventricular tachycardia"}]}},{"entity":"MGI:3525250","phenotype":{"types":[{"id":"MP:0004754","label":"abnormal kidney collecting duct morphology"}]}},{"entity":"ClinVarVariant:42086","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"MGI:3050763","phenotype":{"types":[{"id":"HP:0002180","label":"Neurodegeneration"}]}},{"entity":"ClinVarVariant:7185","phenotype":{"types":[{"id":"HP:0001081","label":"Cholelithiasis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007784-WBRNAi00080092","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:24438","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:194417","phenotype":{"types":[{"id":"HP:0000846","label":"Adrenal insufficiency"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022027-WBRNAi00004763","phenotype":{"types":[{"id":"WBPhenotype:0000644","label":"paralyzed"}]}},{"entity":"ClinVarVariant:159660","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:17484","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"MGI:2183933","phenotype":{"types":[{"id":"MP:0004852","label":"decreased testis weight"}]}},{"entity":"ClinVarVariant:24478","phenotype":{"types":[{"id":"HP:0000517","label":"Abnormality of the lens"}]}},{"entity":"MGI:5440173","phenotype":{"types":[{"id":"HP:0000902","label":"Rib fusion"}]}},{"entity":"ClinVarVariant:186923","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"FlyBase:FBal0242627","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"dbSNP:rs10172646","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:2178057","phenotype":{"types":[{"id":"MP:0001360","label":"abnormal social investigation"}]}},{"entity":"ClinVarVariant:9589","phenotype":{"types":[{"id":"HP:0002352","label":"Leukoencephalopathy"}]}},{"entity":"ClinVarVariant:97524","phenotype":{"types":[{"id":"HP:0000999","label":"Pyoderma"}]}},{"entity":"ClinVarVariant:7411","phenotype":{"types":[{"id":"HP:0001100","label":"Heterochromia iridis"}]}},{"entity":"ClinVarVariant:2218","phenotype":{"types":[{"id":"HP:0100544","label":"Neoplasm of the heart"}]}},{"entity":"FlyBase:FBal0042579","phenotype":{"types":[{"id":"FBcv:0002033","label":"lethal - all die during embryonic stage"}]}},{"entity":"ClinVarVariant:68556","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:5051","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"FlyBase:FBal0284394","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"WormBase:WBVar00089606","phenotype":{"types":[{"id":"WBPhenotype:0000565","label":"coiler"}]}},{"entity":"MGI:2386742","phenotype":{"types":[{"id":"MP:0002834","label":"decreased heart weight"}]}},{"entity":"ClinVarVariant:181956","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"dbSNP:rs1819084","phenotype":{"types":[{"id":"HP:0004798","label":"Recurrent infection of the gastrointestinal tract"}]}},{"entity":"ClinVarVariant:40052","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"ClinVarVariant:120250","phenotype":{"types":[{"id":"HP:0002144","label":"Tethered cord"}]}},{"entity":"ClinVarVariant:53360","phenotype":{"types":[{"id":"HP:0000027","label":"Azoospermia"}]}},{"entity":"MGI:3763247","phenotype":{"types":[{"id":"MP:0002376","label":"abnormal dendritic cell physiology"}]}},{"entity":"dbSNP:rs109025111","phenotype":{"types":[{"id":"AQTLTrait:1153","label":"Stillbirth"}]}},{"entity":"ClinVarVariant:67013","phenotype":{"types":[{"id":"HP:0010536","label":"Central sleep apnea"}]}},{"entity":"ClinVarVariant:4765","phenotype":{"types":[{"id":"HP:0000232","label":"Everted lower lip vermilion"}]}},{"entity":"ClinVarVariant:18242","phenotype":{"types":[{"id":"HP:0009919","label":"Retinoblastoma"}]}},{"entity":"ClinVarVariant:215698","phenotype":{"types":[{"id":"HP:0003468","label":"Abnormality of the vertebrae"}]}},{"entity":"ClinVarVariant:24370","phenotype":{"types":[{"id":"HP:0011508","label":"Macular hole"}]}},{"entity":"ClinVarVariant:11043","phenotype":{"types":[{"id":"HP:0001598","label":"Concave nail"}]}},{"entity":"ClinVarVariant:56602","phenotype":{"types":[{"id":"HP:0007738","label":"Uncontrolled eye movements"}]}},{"entity":"MGI:3811777","phenotype":{"types":[{"id":"MP:0001473","label":"reduced long term potentiation"}]}},{"entity":"ClinVarVariant:7235","phenotype":{"types":[{"id":"HP:0100582","label":"Nasal polyposis"}]}},{"entity":"ClinVarVariant:204077","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:127701","phenotype":{"types":[{"id":"HP:0008204","label":"Precocious puberty with Sertoli cell tumor"}]}},{"entity":"MGI:3513454","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:56677","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"ClinVarVariant:210434","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:66491","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"FlyBase:FBal0208645","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:144065","phenotype":{"types":[{"id":"HP:0011484","label":"Posterior synechiae of the anterior chamber"}]}},{"entity":"ClinVarVariant:3914","phenotype":{"types":[{"id":"HP:0003495","label":"GM2-ganglioside accumulation"}]}},{"entity":"ClinVarVariant:1907","phenotype":{"types":[{"id":"HP:0002416","label":"Subependymal cysts"}]}},{"entity":"FlyBase:FBal0097024","phenotype":{"types":[{"id":"FBbt:00001849PHENOTYPE","label":"hypostomal sclerite phenotype"}]}},{"entity":"MGI:2652160","phenotype":{"types":[{"id":"MP:0002452","label":"abnormal professional antigen presenting cell physiology"}]}},{"entity":"MGI:1926453","phenotype":{"types":[{"id":"MP:0003704","label":"abnormal hair follicle development"}]}},{"entity":"ClinVarVariant:6272","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"FlyBase:FBal0296336","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:65525","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"MGI:1861040","phenotype":{"types":[{"id":"MP:0002389","label":"abnormal Peyer's patch follicle morphology"}]}},{"entity":"ClinVarVariant:3491","phenotype":{"types":[{"id":"HP:0003774","label":"Stage 5 chronic kidney disease"}]}},{"entity":"ClinVarVariant:140916","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:95085","phenotype":{"types":[{"id":"HP:0000954","label":"Single transverse palmar crease"}]}},{"entity":"ClinVarVariant:1470","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:189700","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:35858","phenotype":{"types":[{"id":"HP:0006516","label":"Hypersensitivity pneumonitis"}]}},{"entity":"MGI:2389582","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:135777","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"MGI:2429736","phenotype":{"types":[{"id":"MP:0010776","label":"abnormal placenta metrial gland morphology"}]}},{"entity":"ClinVarVariant:6652","phenotype":{"types":[{"id":"HP:0003741","label":"Congenital muscular dystrophy"}]}},{"entity":"ClinVarVariant:204093","phenotype":{"types":[{"id":"HP:0000112","label":"Nephropathy"}]}},{"entity":"ClinVarVariant:132711","phenotype":{"types":[{"id":"HP:0000706","label":"Unerupted tooth"}]}},{"entity":"_:genid1976000","phenotype":{"types":[{"id":"ZP:0000765","label":"abnormal(ly) increased size optic tectum"}]}},{"entity":"ClinVarVariant:188879","phenotype":{"types":[{"id":"HP:0200032","label":"Kayser-Fleischer ring"}]}},{"entity":"ClinVarVariant:5279","phenotype":{"types":[{"id":"HP:0010978","label":"Abnormality of immune system physiology"}]}},{"entity":"ClinVarVariant:136102","phenotype":{"types":[{"id":"HP:0010829","label":"Impaired temperature sensation"}]}},{"entity":"ClinVarVariant:11456","phenotype":{"types":[{"id":"HP:0000679","label":"Taurodontia"}]}},{"entity":"MGI:5471642","phenotype":{"types":[{"id":"MP:0006042","label":"increased apoptosis"}]}},{"entity":"ClinVarVariant:42357","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"ClinVarVariant:40245","phenotype":{"types":[{"id":"HP:0100775","label":"Dural ectasia"}]}},{"entity":"ClinVarVariant:188801","phenotype":{"types":[{"id":"HP:0001933","label":"Subcutaneous hemorrhage"}]}},{"entity":"ClinVarVariant:180636","phenotype":{"types":[{"id":"HP:0001339","label":"Lissencephaly"}]}},{"entity":"ClinVarVariant:31017","phenotype":{"types":[{"id":"HP:0006439","label":"Radioulnar dislocation"}]}},{"entity":"ClinVarVariant:38932","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:13997","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:155793","phenotype":{"types":[{"id":"HP:0001646","label":"Abnormality of the aortic valve"}]}},{"entity":"ClinVarVariant:10108","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"ClinVarVariant:17346","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"MGI:5297423","phenotype":{"types":[{"id":"HP:0011641","label":"Coronary artery fistula"}]}},{"entity":"dbSNP:rs80934742","phenotype":{"types":[{"id":"AQTLTrait:1181","label":"Muscle pH"}]}},{"entity":"ClinVarVariant:49414","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"NCBIGene:105463128","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"ClinVarVariant:36381","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:1529","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:1087","phenotype":{"types":[{"id":"HP:0001371","label":"Flexion contracture"}]}},{"entity":"ClinVarVariant:184154","phenotype":{"types":[{"id":"HP:0001920","label":"Renal artery stenosis"}]}},{"entity":"FlyBase:FBal0127293","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:67926","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:3961","phenotype":{"types":[{"id":"HP:0000652","label":"Lower eyelid coloboma"}]}},{"entity":"ClinVarVariant:40983","phenotype":{"types":[{"id":"HP:0003025","label":"Metaphyseal irregularity"}]}},{"entity":"ClinVarVariant:3282","phenotype":{"types":[{"id":"HP:0010302","label":"Spinal cord tumor"}]}},{"entity":"ClinVarVariant:1825","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:1115","phenotype":{"types":[{"id":"HP:0000608","label":"Macular degeneration"}]}},{"entity":"ClinVarVariant:25059","phenotype":{"types":[{"id":"HP:0100275","label":"Diffuse cerebellar atrophy"}]}},{"entity":"ClinVarVariant:197758","phenotype":{"types":[{"id":"HP:0001685","label":"Myocardial fibrosis"}]}},{"entity":"ClinVarVariant:210424","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000390-WBRNAi00034721","phenotype":{"types":[{"id":"WBPhenotype:0000700","label":"multivulva"}]}},{"entity":"ClinVarVariant:8953","phenotype":{"types":[{"id":"HP:0000126","label":"Hydronephrosis"}]}},{"entity":"FlyBase:FBal0200755","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:100775","phenotype":{"types":[{"id":"HP:0001371","label":"Flexion contracture"}]}},{"entity":"ClinVarVariant:8746","phenotype":{"types":[{"id":"HP:0009908","label":"Anterior creases of earlobe"}]}},{"entity":"ClinVarVariant:53456","phenotype":{"types":[{"id":"HP:0006538","label":"Recurrent bronchopulmonary infections"}]}},{"entity":"ClinVarVariant:216771","phenotype":{"types":[{"id":"HP:0002385","label":"Paraparesis"}]}},{"entity":"ZFIN:ZDB-ALT-150115-1","phenotype":{"types":[{"id":"ZP:0013924","label":"abnormal(ly) has fewer parts of type spinal cord motor neuron towards motor neuron synapse"}]}},{"entity":"ClinVarVariant:12483","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"ClinVarVariant:41057","phenotype":{"types":[{"id":"HP:0010297","label":"Bifid tongue"}]}},{"entity":"ClinVarVariant:24459","phenotype":{"types":[{"id":"HP:0100273","label":"Neoplasm of the colon"}]}},{"entity":"ClinVarVariant:41112","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:17292","phenotype":{"types":[{"id":"HP:0001518","label":"Small for gestational age"}]}},{"entity":"ClinVarVariant:11826","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"MGI:3526854","phenotype":{"types":[{"id":"MP:0010587","label":"conotruncal ridge hypoplasia"}]}},{"entity":"ClinVarVariant:4024","phenotype":{"types":[{"id":"HP:0000158","label":"Macroglossia"}]}},{"entity":"ClinVarVariant:126402","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:53518","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"NCBIGene:46","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:25235","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"FlyBase:FBal0208051","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:31215","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"MGI:3702579","phenotype":{"types":[{"id":"HP:0005403","label":"T lymphocytopenia"}]}},{"entity":"FlyBase:FBal0042742","phenotype":{"types":[{"id":"FBcv:0002041","label":"some die during embryonic stage"}]}},{"entity":"NCBIGene:2759","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"dbSNP:rs43015698","phenotype":{"types":[{"id":"AQTLTrait:1327","label":"Milk odd-chain fatty acid percentage"}]}},{"entity":"ClinVarVariant:13664","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:101165","phenotype":{"types":[{"id":"HP:0100645","label":"Cystocele"}]}},{"entity":"ClinVarVariant:120291","phenotype":{"types":[{"id":"HP:0001992","label":"Organic aciduria"}]}},{"entity":"ClinVarVariant:10888","phenotype":{"types":[{"id":"HP:0000496","label":"Abnormality of eye movement"}]}},{"entity":"ClinVarVariant:12783","phenotype":{"types":[{"id":"HP:0002668","label":"Paraganglioma"}]}},{"entity":"ClinVarVariant:189202","phenotype":{"types":[{"id":"HP:0001662","label":"Bradycardia"}]}},{"entity":"ClinVarVariant:1114","phenotype":{"types":[{"id":"HP:0001258","label":"Spastic paraplegia"}]}},{"entity":"ClinVarVariant:53933","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:49975","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"MGI:3692444","phenotype":{"types":[{"id":"MP:0011089","label":"perinatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:53448","phenotype":{"types":[{"id":"HP:0100646","label":"Thyroiditis"}]}},{"entity":"ClinVarVariant:101175","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:188802","phenotype":{"types":[{"id":"HP:0100022","label":"Abnormality of movement"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-070206-1-ZDB-MRPHLNO-120719-3","phenotype":{"types":[{"id":"ZP:0003863","label":"abnormal(ly) malformed caudal vein plexus"}]}},{"entity":"FlyBase:FBal0267174","phenotype":{"types":[{"id":"FBcv:0000425","label":"increased cell death"}]}},{"entity":"ClinVarVariant:159086","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:41388","phenotype":{"types":[{"id":"HP:0008069","label":"Neoplasm of the skin"}]}},{"entity":"ClinVarVariant:132731","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:132873","phenotype":{"types":[{"id":"HP:0005059","label":"Arthralgia/arthritis"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-040704-56-ZDB-MRPHLNO-150717-3","phenotype":{"types":[{"id":"GO:0001654PHENOTYPE","label":"eye development phenotype"}]}},{"entity":"dbSNP:rs135873847","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"MGI:1856333","phenotype":{"types":[{"id":"MP:0008917","label":"abnormal oligodendrocyte physiology"}]}},{"entity":"ClinVarVariant:21109","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:95186","phenotype":{"types":[{"id":"HP:0002793","label":"Abnormal pattern of respiration"}]}},{"entity":"ClinVarVariant:2931","phenotype":{"types":[{"id":"HP:0010628","label":"Facial palsy"}]}},{"entity":"FlyBase:FBal0206992","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:53489","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:54034","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"MGI:1926453","phenotype":{"types":[{"id":"MP:0000424","label":"retarded hair growth"}]}},{"entity":"MGI:3577203","phenotype":{"types":[{"id":"MP:0006082","label":"CNS inflammation"}]}},{"entity":"ClinVarVariant:162523","phenotype":{"types":[{"id":"HP:0010055","label":"Broad hallux"}]}},{"entity":"dbSNP:rs1864400","phenotype":{"types":[{"id":"HP:0004401","label":"Meconium ileus"}]}},{"entity":"ClinVarVariant:50259","phenotype":{"types":[{"id":"HP:0002756","label":"Pathologic fracture"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000063-WBRNAi00026183","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"_:genid1974640","phenotype":{"types":[{"id":"ZP:0001504","label":"abnormal(ly) present in fewer numbers in organism myotome skeletal muscle cell"}]}},{"entity":"ClinVarVariant:91660","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:215589","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:102846","phenotype":{"types":[{"id":"HP:0003231","label":"Hypertyrosinemia"}]}},{"entity":"ClinVarVariant:30013","phenotype":{"types":[{"id":"HP:0000294","label":"Low anterior hairline"}]}},{"entity":"ClinVarVariant:10664","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"MGI:3693248","phenotype":{"types":[{"id":"GO:0008016PHENOTYPE","label":"regulation of heart contraction phenotype"}]}},{"entity":"FlyBase:FBal0246629","phenotype":{"types":[{"id":"GO:0030054PHENOTYPE","label":"cell junction phenotype"}]}},{"entity":"MGI:2179534","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"MGI:3689957","phenotype":{"types":[{"id":"MP:0010205","label":"abnormal oligodendrocyte apoptosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007352-WBRNAi00079985","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011747-WBRNAi00073828","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:53610","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:10551","phenotype":{"types":[{"id":"HP:0000597","label":"Ophthalmoparesis"}]}},{"entity":"ClinVarVariant:53330","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:10318","phenotype":{"types":[{"id":"HP:0100614","label":"Myositis"}]}},{"entity":"ClinVarVariant:10063","phenotype":{"types":[{"id":"HP:0007325","label":"Generalized dystonia"}]}},{"entity":"MGI:2183949","phenotype":{"types":[{"id":"HP:0011902","label":"Abnormal hemoglobin"}]}},{"entity":"ClinVarVariant:10736","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"ClinVarVariant:24650","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:177834","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"MGI:3701835","phenotype":{"types":[{"id":"HP:0003687","label":"Centrally nucleated skeletal muscle fibers"}]}},{"entity":"ClinVarVariant:11520","phenotype":{"types":[{"id":"HP:0002007","label":"Frontal bossing"}]}},{"entity":"ClinVarVariant:17491","phenotype":{"types":[{"id":"HP:0000360","label":"Tinnitus"}]}},{"entity":"ClinVarVariant:7445","phenotype":{"types":[{"id":"HP:0100896","label":"Rectal polyposis"}]}},{"entity":"ClinVarVariant:161357","phenotype":{"types":[{"id":"HP:0001166","label":"Arachnodactyly"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004453-WBRNAi00085642","phenotype":{"types":[{"id":"WBPhenotype:0000291","label":"no oocytes"}]}},{"entity":"MGI:2181662","phenotype":{"types":[{"id":"MP:0008515","label":"thin retinal outer nuclear layer"}]}},{"entity":"_:genid1975883","phenotype":{"types":[{"id":"ZP:0000319","label":"abnormal(ly) hydrocephalic brain"}]}},{"entity":"ClinVarVariant:7519","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"MGI:3655845","phenotype":{"types":[{"id":"HP:0007033","label":"Cerebellar dysplasia"}]}},{"entity":"ClinVarVariant:12038","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"_:genid1938554","phenotype":{"types":[{"id":"ZP:0000473","label":"abnormal(ly) decreased length whole organism"}]}},{"entity":"ClinVarVariant:162387","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"MGI:3830289","phenotype":{"types":[{"id":"HP:0001669","label":"Transposition of the great arteries"}]}},{"entity":"dbSNP:rs1953600","phenotype":{"types":[{"id":"HP:0006516","label":"Hypersensitivity pneumonitis"}]}},{"entity":"FlyBase:FBal0199757","phenotype":{"types":[{"id":"FBbt:00004580PHENOTYPE","label":"Drosophila mesothoracic tergum phenotype"}]}},{"entity":"ClinVarVariant:204228","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:1901","phenotype":{"types":[{"id":"HP:0007360","label":"Aplasia/Hypoplasia of the cerebellum"}]}},{"entity":"ClinVarVariant:101364","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"MGI:5641735","phenotype":{"types":[{"id":"MP:0000877","label":"abnormal Purkinje cell morphology"}]}},{"entity":"ClinVarVariant:35895","phenotype":{"types":[{"id":"HP:0006706","label":"Cystic liver disease"}]}},{"entity":"ClinVarVariant:8733","phenotype":{"types":[{"id":"HP:0003128","label":"Lactic acidosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003073-WBRNAi00034975","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:11667","phenotype":{"types":[{"id":"HP:0001187","label":"Hyperextensibility of the finger joints"}]}},{"entity":"FlyBase:FBal0197891","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:143534","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"ClinVarVariant:41696","phenotype":{"types":[{"id":"HP:0009734","label":"Optic glioma"}]}},{"entity":"ClinVarVariant:64974","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:7440","phenotype":{"types":[{"id":"HP:0000069","label":"Abnormality of the ureter"}]}},{"entity":"dbSNP:rs43703486","phenotype":{"types":[{"id":"AQTLTrait:1096","label":"Teat length"}]}},{"entity":"ClinVarVariant:13351","phenotype":{"types":[{"id":"HP:0000391","label":"Thickened helices"}]}},{"entity":"ClinVarVariant:65898","phenotype":{"types":[{"id":"HP:0000939","label":"Osteoporosis"}]}},{"entity":"ClinVarVariant:10068","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"WormBase:WBVar00088666","phenotype":{"types":[{"id":"WBPhenotype:0000012","label":"dauer constitutive"}]}},{"entity":"ClinVarVariant:56031","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:5559","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"MGI:2176775","phenotype":{"types":[{"id":"MP:0002169","label":"no abnormal phenotype detected"}]}},{"entity":"ClinVarVariant:782","phenotype":{"types":[{"id":"HP:0003201","label":"Rhabdomyolysis"}]}},{"entity":"WormBase:WBVar00088241","phenotype":{"types":[{"id":"WBPhenotype:0001351","label":"protein phosphorylation reduced"}]}},{"entity":"ClinVarVariant:42327","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"ClinVarVariant:217027","phenotype":{"types":[{"id":"HP:0000682","label":"Abnormality of dental enamel"}]}},{"entity":"ClinVarVariant:38314","phenotype":{"types":[{"id":"HP:0000046","label":"Scrotal hypoplasia"}]}},{"entity":"ClinVarVariant:7926","phenotype":{"types":[{"id":"HP:0007856","label":"Punctate opacification of the cornea"}]}},{"entity":"ClinVarVariant:53670","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:101202","phenotype":{"types":[{"id":"HP:0005267","label":"Premature delivery because of cervical insufficiency or membrane fragility"}]}},{"entity":"MGI:2450853","phenotype":{"types":[{"id":"HP:0000798","label":"Oligospermia"}]}},{"entity":"ClinVarVariant:136171","phenotype":{"types":[{"id":"HP:0002044","label":"Zollinger-Ellison syndrome"}]}},{"entity":"ClinVarVariant:210444","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:38425","phenotype":{"types":[{"id":"HP:0003264","label":"Deficiency of N-acetylglucosamine-1-phosphotransferase"}]}},{"entity":"ClinVarVariant:96","phenotype":{"types":[{"id":"HP:0000153","label":"Abnormality of the mouth"}]}},{"entity":"ClinVarVariant:24380","phenotype":{"types":[{"id":"HP:0100242","label":"Sarcoma"}]}},{"entity":"ClinVarVariant:7789","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"MGI:2667333","phenotype":{"types":[{"id":"HP:0002733","label":"Abnormality of the lymph nodes"}]}},{"entity":"ClinVarVariant:5590","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:209077","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:2116","phenotype":{"types":[{"id":"HP:0002510","label":"Spastic tetraplegia"}]}},{"entity":"ClinVarVariant:208182","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:54093","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:982","phenotype":{"types":[{"id":"HP:0005105","label":"Abnormal nasal morphology"}]}},{"entity":"ClinVarVariant:39785","phenotype":{"types":[{"id":"HP:0000592","label":"Blue sclerae"}]}},{"entity":"ClinVarVariant:41202","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:11096","phenotype":{"types":[{"id":"HP:0010307","label":"Stridor"}]}},{"entity":"ClinVarVariant:192241","phenotype":{"types":[{"id":"HP:0000734","label":"Disinhibition"}]}},{"entity":"ClinVarVariant:50030","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"dbSNP:rs1953600","phenotype":{"types":[{"id":"HP:0011134","label":"Low-grade fever"}]}},{"entity":"MGI:2678819","phenotype":{"types":[{"id":"MP:0008083","label":"decreased single-positive T cell number"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00044800-WBRNAi00085802","phenotype":{"types":[{"id":"WBPhenotype:0000186","label":"oogenesis variant"}]}},{"entity":"MGI:5293082","phenotype":{"types":[{"id":"HP:0002910","label":"Elevated hepatic transaminases"}]}},{"entity":"ClinVarVariant:209047","phenotype":{"types":[{"id":"HP:0002331","label":"Headache (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:13349","phenotype":{"types":[{"id":"HP:0000465","label":"Webbed neck"}]}},{"entity":"ClinVarVariant:16262","phenotype":{"types":[{"id":"HP:0003759","label":"Hypoplasia of lymphatic vessels"}]}},{"entity":"ClinVarVariant:4320","phenotype":{"types":[{"id":"HP:0003540","label":"Impaired platelet aggregation"}]}},{"entity":"ClinVarVariant:137948","phenotype":{"types":[{"id":"HP:0000768","label":"Pectus carinatum"}]}},{"entity":"ClinVarVariant:11124","phenotype":{"types":[{"id":"HP:0001891","label":"Iron deficiency anemia"}]}},{"entity":"ClinVarVariant:212207","phenotype":{"types":[{"id":"HP:0002015","label":"Dysphagia"}]}},{"entity":"ClinVarVariant:5194","phenotype":{"types":[{"id":"HP:0002694","label":"Sclerosis of skull base"}]}},{"entity":"ClinVarVariant:65750","phenotype":{"types":[{"id":"HP:0001875","label":"Neutropenia"}]}},{"entity":"ClinVarVariant:3843","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:279","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"ClinVarVariant:65513","phenotype":{"types":[{"id":"HP:0000546","label":"Retinal degeneration"}]}},{"entity":"ClinVarVariant:2146","phenotype":{"types":[{"id":"HP:0001377","label":"Limited elbow extension"}]}},{"entity":"FlyBase:FBal0175418","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"FlyBase:FBal0203926","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:208026","phenotype":{"types":[{"id":"HP:0000280","label":"Coarse facial features"}]}},{"entity":"ClinVarVariant:10232","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"ClinVarVariant:200129","phenotype":{"types":[{"id":"HP:0004937","label":"Pulmonary artery aneurysm"}]}},{"entity":"ClinVarVariant:53494","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:5069","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:5145","phenotype":{"types":[{"id":"HP:0008625","label":"Severe sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:40594","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ZFIN:ZDB-ALT-060301-2","phenotype":{"types":[{"id":"ZP:0012481","label":"abnormal(ly) decreased cellular motility branchiomotor neuron"}]}},{"entity":"ClinVarVariant:6292","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:24279","phenotype":{"types":[{"id":"HP:0000613","label":"Photophobia"}]}},{"entity":"ClinVarVariant:10765","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"MGI:3689422","phenotype":{"types":[{"id":"MP:0008302","label":"thin adrenal cortex"}]}},{"entity":"MGI:2387343","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"MGI:3056733","phenotype":{"types":[{"id":"MP:0009820","label":"abnormal liver vasculature morphology"}]}},{"entity":"ClinVarVariant:7215","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:92592","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"MGI:3810526","phenotype":{"types":[{"id":"HP:0005404","label":"Increase in B cell number"}]}},{"entity":"ClinVarVariant:190250","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:215683","phenotype":{"types":[{"id":"HP:0100246","label":"Osteoma"}]}},{"entity":"ClinVarVariant:14924","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:72","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"FlyBase:FBal0262639","phenotype":{"types":[{"id":"FBbt:00000052PHENOTYPE","label":"Drosophila embryo phenotype"}]}},{"entity":"FlyBase:FBal0104352","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"FlyBase:FBal0125070","phenotype":{"types":[{"id":"FBbt:00004511PHENOTYPE","label":"Drosophila antenna phenotype"}]}},{"entity":"MGI:1856555","phenotype":{"types":[{"id":"MP:0004528","label":"fused outer hair cell stereocilia"}]}},{"entity":"ClinVarVariant:132644","phenotype":{"types":[{"id":"HP:0003108","label":"Hyperglycinuria"}]}},{"entity":"ClinVarVariant:67509","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"MGI:5507843","phenotype":{"types":[{"id":"MP:0002084","label":"abnormal developmental patterning"}]}},{"entity":"ClinVarVariant:183434","phenotype":{"types":[{"id":"HP:0000358","label":"Posteriorly rotated ears"}]}},{"entity":"MGI:2183515","phenotype":{"types":[{"id":"MP:0011100","label":"preweaning lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:36320","phenotype":{"types":[{"id":"HP:0011906","label":"Reduced beta/alpha synthesis ratio"}]}},{"entity":"ClinVarVariant:10859","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"AQTL:54067","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:13351","phenotype":{"types":[{"id":"HP:0010935","label":"Abnormality of the upper urinary tract"}]}},{"entity":"ClinVarVariant:158279","phenotype":{"types":[{"id":"HP:0006191","label":"Deep palmar crease"}]}},{"entity":"ClinVarVariant:41145","phenotype":{"types":[{"id":"HP:0000286","label":"Epicanthus"}]}},{"entity":"ClinVarVariant:185834","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:1856328","phenotype":{"types":[{"id":"MP:0013237","label":"abnormal skeletal muscle regeneration"}]}},{"entity":"ClinVarVariant:217049","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:12690","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:13949","phenotype":{"types":[{"id":"HP:0000843","label":"Hyperparathyroidism"}]}},{"entity":"MGI:1856197","phenotype":{"types":[{"id":"MP:0006371","label":"absent hair follicle pheomelanosome pheomelanin"}]}},{"entity":"ClinVarVariant:53229","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"ClinVarVariant:143582","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:210446","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"ClinVarVariant:10146","phenotype":{"types":[{"id":"HP:0005261","label":"Joint hemorrhage"}]}},{"entity":"ClinVarVariant:54044","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"MGI:1856009","phenotype":{"types":[{"id":"HP:0000855","label":"Insulin resistance"}]}},{"entity":"ClinVarVariant:40680","phenotype":{"types":[{"id":"HP:0001595","label":"Abnormality of the hair"}]}},{"entity":"ClinVarVariant:167487","phenotype":{"types":[{"id":"HP:0005576","label":"Tubulointerstitial fibrosis"}]}},{"entity":"ClinVarVariant:17322","phenotype":{"types":[{"id":"HP:0002659","label":"Increased susceptibility to fractures"}]}},{"entity":"ClinVarVariant:8212","phenotype":{"types":[{"id":"HP:0100730","label":"Bronchogenic cyst"}]}},{"entity":"ClinVarVariant:156529","phenotype":{"types":[{"id":"HP:0011950","label":"Bronchiolitis"}]}},{"entity":"ClinVarVariant:210464","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:159157","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"ClinVarVariant:25225","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"MGI:1889570","phenotype":{"types":[{"id":"GO:0006112PHENOTYPE","label":"energy reserve metabolic process phenotype"}]}},{"entity":"ClinVarVariant:53366","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:167138","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:30835","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"NCBIGene:100188340","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:906","phenotype":{"types":[{"id":"HP:0002721","label":"Immunodeficiency"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-991124-7-ZDB-MRPHLNO-060328-3","phenotype":{"types":[{"id":"ZP:0008625","label":"abnormal(ly) physical object quality pectoral fin"}]}},{"entity":"MGI:2182273","phenotype":{"types":[{"id":"HP:0005403","label":"T lymphocytopenia"}]}},{"entity":"ClinVarVariant:2712","phenotype":{"types":[{"id":"HP:0000268","label":"Dolichocephaly"}]}},{"entity":"ClinVarVariant:1655","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:49520","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:159216","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:180362","phenotype":{"types":[{"id":"HP:0000166","label":"Severe periodontitis"}]}},{"entity":"ClinVarVariant:2687","phenotype":{"types":[{"id":"HP:0001297","label":"Stroke"}]}},{"entity":"ClinVarVariant:41224","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ClinVarVariant:190257","phenotype":{"types":[{"id":"HP:0100646","label":"Thyroiditis"}]}},{"entity":"ClinVarVariant:4364","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"ClinVarVariant:143482","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:36962","phenotype":{"types":[{"id":"HP:0002652","label":"Skeletal dysplasia"}]}},{"entity":"ClinVarVariant:65377","phenotype":{"types":[{"id":"HP:0009734","label":"Optic glioma"}]}},{"entity":"FlyBase:FBal0051183","phenotype":{"types":[{"id":"FBcv:0002000","label":"lethal - all die before end of P-stage"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050208-123-ZDB-MRPHLNO-150410-1-ZDB-MRPHLNO-150424-1","phenotype":{"types":[{"id":"ZP:0001849","label":"abnormal(ly) present in greater numbers in organism pronephros multi-ciliated epithelial cell"}]}},{"entity":"ClinVarVariant:103","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:6619","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"AQTL:44271","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:40555","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:12483","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"ClinVarVariant:41882","phenotype":{"types":[{"id":"HP:0001321","label":"Cerebellar hypoplasia"}]}},{"entity":"ClinVarVariant:42347","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"MGI:2384332","phenotype":{"types":[{"id":"MP:0003921","label":"abnormal heart left ventricle morphology"}]}},{"entity":"ClinVarVariant:53206","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:24468","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:16424","phenotype":{"types":[{"id":"HP:0100749","label":"Chest pain"}]}},{"entity":"ClinVarVariant:16875","phenotype":{"types":[{"id":"HP:0003325","label":"Limb-girdle muscle weakness"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-030127-1-ZDB-MRPHLNO-051221-6","phenotype":{"types":[{"id":"ZP:0000132","label":"abnormal(ly) malformed ceratohyal cartilage"}]}},{"entity":"ClinVarVariant:53974","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:53710","phenotype":{"types":[{"id":"HP:0011892","label":"Vitamin K deficiency"}]}},{"entity":"ClinVarVariant:142434","phenotype":{"types":[{"id":"HP:0002073","label":"Progressive cerebellar ataxia"}]}},{"entity":"ClinVarVariant:13055","phenotype":{"types":[{"id":"HP:0001123","label":"Visual field defect"}]}},{"entity":"ClinVarVariant:24782","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:157934","phenotype":{"types":[{"id":"HP:0001433","label":"Hepatosplenomegaly"}]}},{"entity":"MGI:2150685","phenotype":{"types":[{"id":"MP:0004616","label":"lumbar vertebral transformation"}]}},{"entity":"ClinVarVariant:11962","phenotype":{"types":[{"id":"HP:0000090","label":"Nephronophthisis"}]}},{"entity":"ClinVarVariant:13394","phenotype":{"types":[{"id":"HP:0002381","label":"Aphasia"}]}},{"entity":"MGI:3574394","phenotype":{"types":[{"id":"HP:0005180","label":"Tricuspid regurgitation"}]}},{"entity":"ClinVarVariant:13369","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"AQTL:23249","phenotype":{"types":[{"id":"AQTLTrait:1252","label":"Milk myristic acid percentage"}]}},{"entity":"ClinVarVariant:42400","phenotype":{"types":[{"id":"HP:0000646","label":"Amblyopia"}]}},{"entity":"ClinVarVariant:5540","phenotype":{"types":[{"id":"HP:0100726","label":"Kaposi's sarcoma"}]}},{"entity":"MGI:3576366","phenotype":{"types":[{"id":"MP:0009503","label":"abnormal mammary gland duct morphology"}]}},{"entity":"ClinVarVariant:143094","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"ClinVarVariant:48927","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"MGI:3580645","phenotype":{"types":[{"id":"MP:0009004","label":"progressive hair loss"}]}},{"entity":"ClinVarVariant:142003","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:56607","phenotype":{"types":[{"id":"HP:0004327","label":"Abnormality of the vitreous humor"}]}},{"entity":"ClinVarVariant:136164","phenotype":{"types":[{"id":"HP:0000825","label":"Hyperinsulinemic hypoglycemia"}]}},{"entity":"MGI:2670437","phenotype":{"types":[{"id":"MP:0000886","label":"abnormal cerebellar granule layer morphology"}]}},{"entity":"ClinVarVariant:167723","phenotype":{"types":[{"id":"HP:0002894","label":"Neoplasm of the pancreas"}]}},{"entity":"ClinVarVariant:17344","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:41212","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:209049","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"dbSNP:rs29013986","phenotype":{"types":[{"id":"AQTLTrait:1169","label":"Interval to first estrus after calving"}]}},{"entity":"ClinVarVariant:210454","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"MGI:1857966","phenotype":{"types":[{"id":"HP:0001402","label":"Hepatocellular carcinoma"}]}},{"entity":"ClinVarVariant:56243","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:208006","phenotype":{"types":[{"id":"HP:0002748","label":"Rickets"}]}},{"entity":"ClinVarVariant:139531","phenotype":{"types":[{"id":"HP:0012588","label":"Steroid-resistant nephrotic syndrome"}]}},{"entity":"ClinVarVariant:56191","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:49423","phenotype":{"types":[{"id":"HP:0009734","label":"Optic glioma"}]}},{"entity":"ClinVarVariant:11712","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:53393","phenotype":{"types":[{"id":"HP:0006530","label":"Interstitial pulmonary disease"}]}},{"entity":"FlyBase:FBal0297079","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"FlyBase:FBal0200543","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:92359","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ZFIN:ZDB-ALT-030919-2","phenotype":{"types":[{"id":"ZP:0006939","label":"abnormal(ly) has fewer parts of type spinal cord towards motor neuron"}]}},{"entity":"ClinVarVariant:216475","phenotype":{"types":[{"id":"HP:0100641","label":"Neoplasm of the adrenal cortex"}]}},{"entity":"ClinVarVariant:29874","phenotype":{"types":[{"id":"HP:0000580","label":"Pigmentary retinopathy"}]}},{"entity":"ClinVarVariant:10830","phenotype":{"types":[{"id":"HP:0003502","label":"Mild short stature"}]}},{"entity":"ClinVarVariant:95023","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:195913","phenotype":{"types":[{"id":"HP:0002342","label":"Intellectual disability, moderate"}]}},{"entity":"MGI:2387957","phenotype":{"types":[{"id":"MP:0001501","label":"abnormal sleep pattern"}]}},{"entity":"MGI:2386680","phenotype":{"types":[{"id":"GO:0042127PHENOTYPE","label":"regulation of cell proliferation phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00077732-WBRNAi00085693","phenotype":{"types":[{"id":"WBPhenotype:0001973","label":"germ cell compartment size variant"}]}},{"entity":"ClinVarVariant:135735","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008686-WBRNAi00074140","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:12403","phenotype":{"types":[{"id":"HP:0009720","label":"Adenoma sebaceum"}]}},{"entity":"MGI:5312925","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"FlyBase:FBal0202682","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:9886","phenotype":{"types":[{"id":"HP:0007984","label":"Reduced amplitude of dark-adapted bright flash electroretinogram b-wave"}]}},{"entity":"ClinVarVariant:1147","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:93888","phenotype":{"types":[{"id":"HP:0001558","label":"Decreased fetal movement"}]}},{"entity":"FlyBase:FBal0304813","phenotype":{"types":[{"id":"FBcv:0000366","label":"female sterile"}]}},{"entity":"MGI:1857056","phenotype":{"types":[{"id":"MP:0006396","label":"decreased long bone epiphyseal plate size"}]}},{"entity":"ClinVarVariant:53989","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:49828","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-041116-2-ZDB-MRPHLNO-150216-1-ZDB-MRPHLNO-150216-2","phenotype":{"types":[{"id":"ZP:0012064","label":"abnormal(ly) decreased occurrence adenohypophysis corticotropin hormone secreting cell differentiation"}]}},{"entity":"ClinVarVariant:2679","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"MGI:2671317","phenotype":{"types":[{"id":"MP:0011089","label":"perinatal lethality, complete penetrance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004808-WBRNAi00072509","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:93457","phenotype":{"types":[{"id":"HP:0001873","label":"Thrombocytopenia"}]}},{"entity":"ClinVarVariant:1563","phenotype":{"types":[{"id":"HP:0003309","label":"Ovoid thoracolumbar vertebrae"}]}},{"entity":"ClinVarVariant:159086","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"MGI:4365388","phenotype":{"types":[{"id":"MP:0009793","label":"sebaceous gland hypertrophy"}]}},{"entity":"ClinVarVariant:198219","phenotype":{"types":[{"id":"HP:0000590","label":"Progressive external ophthalmoplegia"}]}},{"entity":"dbSNP:rs110304690","phenotype":{"types":[{"id":"AQTLTrait:1101","label":"Foot angle"}]}},{"entity":"ClinVarVariant:7982","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:7141","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"AQTL:35966","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:9970","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:101176","phenotype":{"types":[{"id":"HP:0000387","label":"Absent earlobe"}]}},{"entity":"ClinVarVariant:162666","phenotype":{"types":[{"id":"HP:0011950","label":"Bronchiolitis"}]}},{"entity":"MGI:1856681","phenotype":{"types":[{"id":"MP:0002855","label":"abnormal cochlear ganglion morphology"}]}},{"entity":"ClinVarVariant:67987","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"MGI:4946645","phenotype":{"types":[{"id":"MP:0000947","label":"convulsive seizures"}]}},{"entity":"ClinVarVariant:4268","phenotype":{"types":[{"id":"HP:0004370","label":"Abnormality of temperature regulation"}]}},{"entity":"ClinVarVariant:11356","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"ClinVarVariant:4439","phenotype":{"types":[{"id":"HP:0002317","label":"Unsteady gait"}]}},{"entity":"ClinVarVariant:11002","phenotype":{"types":[{"id":"HP:0001298","label":"Encephalopathy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002845-WBRNAi00064383","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"ClinVarVariant:132848","phenotype":{"types":[{"id":"HP:0000023","label":"Inguinal hernia"}]}},{"entity":"ClinVarVariant:209057","phenotype":{"types":[{"id":"HP:0002331","label":"Headache (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:10175","phenotype":{"types":[{"id":"HP:0011892","label":"Vitamin K deficiency"}]}},{"entity":"dbSNP:rs29025964","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:49552","phenotype":{"types":[{"id":"HP:0009554","label":"Projection of scalp hair onto lateral cheek"}]}},{"entity":"MGI:3578093","phenotype":{"types":[{"id":"HP:0001978","label":"Extramedullary hematopoiesis"}]}},{"entity":"_:genid1975192","phenotype":{"types":[{"id":"ZP:0004393","label":"abnormal(ly) truncated intersegmental vessel"}]}},{"entity":"ClinVarVariant:17312","phenotype":{"types":[{"id":"HP:0002659","label":"Increased susceptibility to fractures"}]}},{"entity":"ClinVarVariant:10154","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:30150","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:17324","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:216201","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:38497","phenotype":{"types":[{"id":"HP:0002017","label":"Nausea and vomiting"}]}},{"entity":"ClinVarVariant:126384","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"ClinVarVariant:13938","phenotype":{"types":[{"id":"HP:0100835","label":"Benign neoplasm of the central nervous system"}]}},{"entity":"MGI:3623342","phenotype":{"types":[{"id":"MP:0011967","label":"increased or absent threshold for auditory brainstem response"}]}},{"entity":"ClinVarVariant:188826","phenotype":{"types":[{"id":"HP:0002352","label":"Leukoencephalopathy"}]}},{"entity":"ClinVarVariant:11359","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:43167","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"AQTL:43115","phenotype":{"types":[{"id":"AQTLTrait:1112","label":"Withers height"}]}},{"entity":"MGI:5502178","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"ClinVarVariant:24217","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:17314","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:139523","phenotype":{"types":[{"id":"HP:0001480","label":"Freckling"}]}},{"entity":"ClinVarVariant:215634","phenotype":{"types":[{"id":"HP:0001017","label":"Anemic pallor"}]}},{"entity":"ClinVarVariant:210454","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:1535","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:5691","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"NCBIGene:57788","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:10717","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"ClinVarVariant:53820","phenotype":{"types":[{"id":"HP:0100513","label":"Vitamin E deficiency"}]}},{"entity":"ClinVarVariant:189569","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"MGI:3512143","phenotype":{"types":[{"id":"HP:0003468","label":"Abnormality of the vertebrae"}]}},{"entity":"ClinVarVariant:6718","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:9581","phenotype":{"types":[{"id":"HP:0000602","label":"Ophthalmoplegia"}]}},{"entity":"ClinVarVariant:4306","phenotype":{"types":[{"id":"HP:0100787","label":"Prostate neoplasm"}]}},{"entity":"ClinVarVariant:50861","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:3408","phenotype":{"types":[{"id":"HP:0000982","label":"Palmoplantar keratoderma"}]}},{"entity":"MGI:4361197","phenotype":{"types":[{"id":"MP:0010168","label":"increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number"}]}},{"entity":"_:genid1975962","phenotype":{"types":[{"id":"ZP:0001173","label":"abnormal(ly) decreased pigmentation whole organism"}]}},{"entity":"ClinVarVariant:208016","phenotype":{"types":[{"id":"HP:0002748","label":"Rickets"}]}},{"entity":"ClinVarVariant:53905","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:11586","phenotype":{"types":[{"id":"HP:0002860","label":"Squamous cell carcinoma"}]}},{"entity":"ClinVarVariant:30467","phenotype":{"types":[{"id":"HP:0002949","label":"Fused cervical vertebrae"}]}},{"entity":"ClinVarVariant:809","phenotype":{"types":[{"id":"HP:0000706","label":"Unerupted tooth"}]}},{"entity":"MGI:2183813","phenotype":{"types":[{"id":"MP:0000646","label":"enlarged adrenocortical cells"}]}},{"entity":"ClinVarVariant:64943","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"ClinVarVariant:3904","phenotype":{"types":[{"id":"HP:0003495","label":"GM2-ganglioside accumulation"}]}},{"entity":"MGI:3653699","phenotype":{"types":[{"id":"HP:0005048","label":"Synostosis of carpal bones"}]}},{"entity":"MGI:5559460","phenotype":{"types":[{"id":"MP:0001666","label":"abnormal intestinal absorption"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004498-WBRNAi00099563","phenotype":{"types":[{"id":"WBPhenotype:0000961","label":"pattern of transgene expression variant"}]}},{"entity":"ClinVarVariant:101394","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:10345","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:4933","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:49479","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"ClinVarVariant:212265","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:49115","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:15234","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00012221-WBRNAi00097504","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:209067","phenotype":{"types":[{"id":"HP:0002331","label":"Headache (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:1257","phenotype":{"types":[{"id":"HP:0000926","label":"Platyspondyly"}]}},{"entity":"ClinVarVariant:36379","phenotype":{"types":[{"id":"HP:0000684","label":"Delayed eruption of teeth"}]}},{"entity":"AQTL:15392","phenotype":{"types":[{"id":"AQTLTrait:1076","label":"Gestation length"}]}},{"entity":"ClinVarVariant:92880","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:694","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"ClinVarVariant:209043","phenotype":{"types":[{"id":"HP:0001115","label":"Posterior polar cataract"}]}},{"entity":"ClinVarVariant:35838","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"ClinVarVariant:216398","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:10122","phenotype":{"types":[{"id":"HP:0100310","label":"Epidural hemorrhage"}]}},{"entity":"ClinVarVariant:17784","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"FlyBase:FBal0033446","phenotype":{"types":[{"id":"FBbt:00000004PHENOTYPE","label":"Drosophila head phenotype"}]}},{"entity":"MGI:3526165","phenotype":{"types":[{"id":"GO:0032880PHENOTYPE","label":"regulation of protein localization phenotype"}]}},{"entity":"ClinVarVariant:210447","phenotype":{"types":[{"id":"HP:0005599","label":"Hypopigmentation of hair"}]}},{"entity":"ClinVarVariant:10285","phenotype":{"types":[{"id":"HP:0001369","label":"Arthritis"}]}},{"entity":"ClinVarVariant:126394","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"ClinVarVariant:9599","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:216023","phenotype":{"types":[{"id":"HP:0000035","label":"Abnormality of the testis"}]}},{"entity":"ClinVarVariant:10738","phenotype":{"types":[{"id":"HP:0000763","label":"Sensory neuropathy"}]}},{"entity":"ClinVarVariant:3571","phenotype":{"types":[{"id":"HP:0010044","label":"Short 4th metacarpal"}]}},{"entity":"ClinVarVariant:67881","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:8710","phenotype":{"types":[{"id":"HP:0002823","label":"Abnormality of the femur"}]}},{"entity":"ClinVarVariant:159228","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"ClinVarVariant:36081","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:161334","phenotype":{"types":[{"id":"HP:0005293","label":"Venous insufficiency"}]}},{"entity":"MGI:3762530","phenotype":{"types":[{"id":"MP:0002020","label":"increased tumor incidence"}]}},{"entity":"ClinVarVariant:188302","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:11342","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"ClinVarVariant:10751","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:53923","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"MGI:5320577","phenotype":{"types":[{"id":"MP:0006059","label":"decreased susceptibility to ischemic brain injury"}]}},{"entity":"ClinVarVariant:17332","phenotype":{"types":[{"id":"HP:0002659","label":"Increased susceptibility to fractures"}]}},{"entity":"ClinVarVariant:66101","phenotype":{"types":[{"id":"HP:0011109","label":"Chronic sinusitis"}]}},{"entity":"ClinVarVariant:11596","phenotype":{"types":[{"id":"HP:0002860","label":"Squamous cell carcinoma"}]}},{"entity":"ClinVarVariant:13848","phenotype":{"types":[{"id":"HP:0007542","label":"Absent pigmentation of the ventral chest"}]}},{"entity":"ClinVarVariant:209019","phenotype":{"types":[{"id":"HP:0000777","label":"Abnormality of the thymus"}]}},{"entity":"ClinVarVariant:166927","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"AQTL:4620","phenotype":{"types":[{"id":"AQTLTrait:1099","label":"Milking speed"}]}},{"entity":"ClinVarVariant:53677","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:159171","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"ClinVarVariant:17976","phenotype":{"types":[{"id":"HP:0006530","label":"Interstitial pulmonary disease"}]}},{"entity":"ClinVarVariant:39444","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:96580","phenotype":{"types":[{"id":"HP:0002179","label":"Opisthotonus"}]}},{"entity":"MGI:1856097","phenotype":{"types":[{"id":"MP:0010908","label":"dilated pulmonary alveolar ducts"}]}},{"entity":"ClinVarVariant:7314","phenotype":{"types":[{"id":"HP:0000678","label":"Dental crowding"}]}},{"entity":"ClinVarVariant:158904","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:215720","phenotype":{"types":[{"id":"HP:0100697","label":"Neurofibrosarcoma"}]}},{"entity":"MGI:2384515","phenotype":{"types":[{"id":"MP:0001405","label":"impaired coordination"}]}},{"entity":"MGI:3576024","phenotype":{"types":[{"id":"HP:0000157","label":"Abnormality of the tongue"}]}},{"entity":"ClinVarVariant:21535","phenotype":{"types":[{"id":"HP:0001256","label":"Intellectual disability, mild"}]}},{"entity":"ClinVarVariant:192298","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"ClinVarVariant:215688","phenotype":{"types":[{"id":"HP:0003468","label":"Abnormality of the vertebrae"}]}},{"entity":"dbSNP:rs110801629","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ZFIN:ZDB-ALT-980203-452","phenotype":{"types":[{"id":"ZP:0000148","label":"abnormal(ly) increased width notochord"}]}},{"entity":"ClinVarVariant:209053","phenotype":{"types":[{"id":"HP:0001648","label":"Cor pulmonale"}]}},{"entity":"ClinVarVariant:30527","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ZFIN:ZDB-ALT-020422-8","phenotype":{"types":[{"id":"ZP:0002275","label":"abnormal(ly) necrotic trunk"}]}},{"entity":"ClinVarVariant:10249","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:101204","phenotype":{"types":[{"id":"HP:0010318","label":"Aplasia/Hypoplasia of the abdominal wall musculature"}]}},{"entity":"ClinVarVariant:9956","phenotype":{"types":[{"id":"HP:0001923","label":"Reticulocytosis"}]}},{"entity":"ClinVarVariant:126447","phenotype":{"types":[{"id":"HP:0100689","label":"Decreased corneal thickness"}]}},{"entity":"ClinVarVariant:93336","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:36957","phenotype":{"types":[{"id":"HP:0001539","label":"Omphalocele"}]}},{"entity":"ClinVarVariant:190118","phenotype":{"types":[{"id":"HP:0002015","label":"Dysphagia"}]}},{"entity":"ClinVarVariant:210474","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:159234","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:40522","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:605","phenotype":{"types":[{"id":"HP:0004923","label":"Hyperphenylalaninemia"}]}},{"entity":"MGI:2155766","phenotype":{"types":[{"id":"MP:0002836","label":"abnormal chorion morphology"}]}},{"entity":"MGI:3511363","phenotype":{"types":[{"id":"HP:0001539","label":"Omphalocele"}]}},{"entity":"ClinVarVariant:41344","phenotype":{"types":[{"id":"HP:0007067","label":"Distal peripheral sensory neuropathy"}]}},{"entity":"ClinVarVariant:38578","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"MGI:4842477","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:82347","phenotype":{"types":[{"id":"HP:0006753","label":"Neoplasm of the stomach"}]}},{"entity":"MGI:1856222","phenotype":{"types":[{"id":"MP:0002938","label":"white spotting"}]}},{"entity":"ClinVarVariant:49718","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"MGI:2652711","phenotype":{"types":[{"id":"MP:0011750","label":"abnormal seminiferous tubule epithelium morphology"}]}},{"entity":"MGI:3056917","phenotype":{"types":[{"id":"MP:0001402","label":"hypoactivity"}]}},{"entity":"MGI:2158307","phenotype":{"types":[{"id":"MP:0002722","label":"abnormal immune system organ morphology"}]}},{"entity":"ClinVarVariant:40526","phenotype":{"types":[{"id":"HP:0000520","label":"Proptosis"}]}},{"entity":"ClinVarVariant:41247","phenotype":{"types":[{"id":"HP:0003429","label":"CNS hypomyelination"}]}},{"entity":"ClinVarVariant:53618","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"FlyBase:FBal0207560","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:216725","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:158962","phenotype":{"types":[{"id":"HP:0011308","label":"Slender toe"}]}},{"entity":"MGI:4880750","phenotype":{"types":[{"id":"MP:0008702","label":"increased interleukin-5 secretion"}]}},{"entity":"AQTL:23951","phenotype":{"types":[{"id":"AQTLTrait:1196","label":"Abomasum displacement"}]}},{"entity":"MGI:1929775","phenotype":{"types":[{"id":"MP:0008148","label":"abnormal rib-sternum attachment"}]}},{"entity":"ClinVarVariant:53716","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:36083","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:88836","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:35713","phenotype":{"types":[{"id":"HP:0000934","label":"Chondrocalcinosis"}]}},{"entity":"ClinVarVariant:190232","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"ClinVarVariant:190368","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:156281","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:210008","phenotype":{"types":[{"id":"HP:0002301","label":"Hemiplegia"}]}},{"entity":"ClinVarVariant:56669","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:8259","phenotype":{"types":[{"id":"HP:0001056","label":"Milia"}]}},{"entity":"ClinVarVariant:10619","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:135769","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:25004","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"MGI:1856699","phenotype":{"types":[{"id":"MP:0001212","label":"skin lesions"}]}},{"entity":"ClinVarVariant:10217","phenotype":{"types":[{"id":"HP:0011892","label":"Vitamin K deficiency"}]}},{"entity":"ClinVarVariant:60779","phenotype":{"types":[{"id":"HP:0008180","label":"Mildly elevated creatine phosphokinase"}]}},{"entity":"ClinVarVariant:53779","phenotype":{"types":[{"id":"HP:0100660","label":"Dyskinesia"}]}},{"entity":"ClinVarVariant:24687","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:100728","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ClinVarVariant:156381","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:41692","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"FlyBase:FBal0126487","phenotype":{"types":[{"id":"FBbt:00001682PHENOTYPE","label":"Drosophila embryonic/larval hemocoel phenotype"}]}},{"entity":"ClinVarVariant:52398","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006700-WBRNAi00061477","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"ClinVarVariant:183367","phenotype":{"types":[{"id":"HP:0005218","label":"Anoperineal fistula"}]}},{"entity":"ClinVarVariant:2482","phenotype":{"types":[{"id":"HP:0001608","label":"Abnormality of the voice"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001892-WBRNAi00025035","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:42345","phenotype":{"types":[{"id":"HP:0004933","label":"Ascending aortic dissection"}]}},{"entity":"ClinVarVariant:9983","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:21565","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:5633","phenotype":{"types":[{"id":"HP:0000141","label":"Amenorrhea"}]}},{"entity":"ClinVarVariant:16624","phenotype":{"types":[{"id":"HP:0003762","label":"Uterus didelphys"}]}},{"entity":"ClinVarVariant:181715","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:199203","phenotype":{"types":[{"id":"HP:0002486","label":"Myotonia"}]}},{"entity":"ClinVarVariant:53715","phenotype":{"types":[{"id":"HP:0004936","label":"Venous thrombosis"}]}},{"entity":"ClinVarVariant:209059","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:56253","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:14091","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:12493","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"MGI:5468098","phenotype":{"types":[{"id":"HP:0011849","label":"Abnormal bone ossification"}]}},{"entity":"MGI:5443922","phenotype":{"types":[{"id":"HP:0003233","label":"Hypoalphalipoproteinemia"}]}},{"entity":"ClinVarVariant:207574","phenotype":{"types":[{"id":"HP:0002495","label":"Impaired vibratory sensation"}]}},{"entity":"WormBase:WBVar00242117","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:53226","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:11430","phenotype":{"types":[{"id":"HP:0008839","label":"Hypoplastic pelvis"}]}},{"entity":"ClinVarVariant:10058","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"ClinVarVariant:158385","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"MGI:5141269","phenotype":{"types":[{"id":"HP:0002591","label":"Polyphagia"}]}},{"entity":"ClinVarVariant:181494","phenotype":{"types":[{"id":"HP:0010541","label":"Cutis gyrata of scalp"}]}},{"entity":"ClinVarVariant:12391","phenotype":{"types":[{"id":"HP:0011364","label":"White hair"}]}},{"entity":"ClinVarVariant:53911","phenotype":{"types":[{"id":"HP:0003453","label":"Antineutrophil antibody positivity"}]}},{"entity":"MGI:2151589","phenotype":{"types":[{"id":"MP:0009355","label":"increased liver triglyceride level"}]}},{"entity":"ClinVarVariant:38415","phenotype":{"types":[{"id":"HP:0003264","label":"Deficiency of N-acetylglucosamine-1-phosphotransferase"}]}},{"entity":"ClinVarVariant:30832","phenotype":{"types":[{"id":"HP:0100790","label":"Hernia"}]}},{"entity":"FlyBase:FBal0209815","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:180622","phenotype":{"types":[{"id":"HP:0004430","label":"Severe combined immunodeficiency"}]}},{"entity":"ClinVarVariant:24371","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"ClinVarVariant:156327","phenotype":{"types":[{"id":"HP:0100512","label":"Vitamin D deficiency"}]}},{"entity":"ClinVarVariant:54054","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:197080","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"MGI:4358721","phenotype":{"types":[{"id":"MP:0001523","label":"impaired righting response"}]}},{"entity":"ClinVarVariant:199965","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"ClinVarVariant:29","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"MGI:3623117","phenotype":{"types":[{"id":"MP:0004918","label":"abnormal negative T cell selection"}]}},{"entity":"ClinVarVariant:158914","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:30626","phenotype":{"types":[{"id":"HP:0100532","label":"Scleritis"}]}},{"entity":"ClinVarVariant:53187","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"FlyBase:FBal0043110","phenotype":{"types":[{"id":"FBbt:00000169PHENOTYPE","label":"embryonic mesothoracic segment phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017282-WBRNAi00102984","phenotype":{"types":[{"id":"WBPhenotype:0000462","label":"paraquat hypersensitive"}]}},{"entity":"ClinVarVariant:53320","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"MGI:3639295","phenotype":{"types":[{"id":"HP:0011121","label":"Abnormality of skin morphology"}]}},{"entity":"ClinVarVariant:215752","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"ClinVarVariant:215780","phenotype":{"types":[{"id":"HP:0003241","label":"External genital hypoplasia"}]}},{"entity":"ClinVarVariant:91650","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:55948","phenotype":{"types":[{"id":"HP:0006887","label":"Intellectual disability, progressive"}]}},{"entity":"ClinVarVariant:17209","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"ClinVarVariant:1461","phenotype":{"types":[{"id":"HP:0006597","label":"Diaphragmatic paralysis"}]}},{"entity":"ClinVarVariant:4310","phenotype":{"types":[{"id":"HP:0003540","label":"Impaired platelet aggregation"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00194986-WBRNAi00085581","phenotype":{"types":[{"id":"WBPhenotype:0001951","label":"pachytene region organization variant"}]}},{"entity":"ClinVarVariant:5069","phenotype":{"types":[{"id":"HP:0100716","label":"Self-injurious behavior"}]}},{"entity":"ClinVarVariant:11644","phenotype":{"types":[{"id":"HP:0000395","label":"Prominent antihelix"}]}},{"entity":"ClinVarVariant:210461","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:217066","phenotype":{"types":[{"id":"HP:0009736","label":"Tibial pseudoarthrosis"}]}},{"entity":"ClinVarVariant:41306","phenotype":{"types":[{"id":"HP:0011449","label":"Knee clonus"}]}},{"entity":"ClinVarVariant:216230","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:16085","phenotype":{"types":[{"id":"HP:0007495","label":"Prematurely aged appearance"}]}},{"entity":"MGI:3785252","phenotype":{"types":[{"id":"MP:0008874","label":"decreased physiological sensitivity to xenobiotic"}]}},{"entity":"_:genid1975900","phenotype":{"types":[{"id":"ZP:0000038","label":"abnormal(ly) edematous pericardium"}]}},{"entity":"ClinVarVariant:11540","phenotype":{"types":[{"id":"HP:0002007","label":"Frontal bossing"}]}},{"entity":"MGI:3624263","phenotype":{"types":[{"id":"MP:0011186","label":"abnormal visceral endoderm morphology"}]}},{"entity":"ClinVarVariant:53939","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ClinVarVariant:156552","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"ClinVarVariant:24978","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:41131","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:36033","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"FlyBase:FBal0210612","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:2149","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ClinVarVariant:24396","phenotype":{"types":[{"id":"HP:0008063","label":"Aplasia/Hypoplasia of the lens"}]}},{"entity":"ClinVarVariant:24651","phenotype":{"types":[{"id":"HP:0011501","label":"Anterior lenticonus"}]}},{"entity":"ClinVarVariant:24375","phenotype":{"types":[{"id":"HP:0000093","label":"Proteinuria"}]}},{"entity":"ClinVarVariant:25310","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:40502","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"ClinVarVariant:167188","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:2128","phenotype":{"types":[{"id":"HP:0000612","label":"Iris coloboma"}]}},{"entity":"MGI:2385717","phenotype":{"types":[{"id":"MP:0002961","label":"abnormal axon guidance"}]}},{"entity":"MGI:2683050","phenotype":{"types":[{"id":"HP:0004324","label":"Increased body weight"}]}},{"entity":"ClinVarVariant:50055","phenotype":{"types":[{"id":"HP:0009716","label":"Subependymal nodules"}]}},{"entity":"ClinVarVariant:7853","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"ClinVarVariant:142534","phenotype":{"types":[{"id":"HP:0001562","label":"Oligohydramnios"}]}},{"entity":"MGI:5470094","phenotype":{"types":[{"id":"HP:0002450","label":"Abnormal motor neuron morphology"}]}},{"entity":"MGI:5441311","phenotype":{"types":[{"id":"MP:0009763","label":"increased sensitivity to induced morbidity/mortality"}]}},{"entity":"MGI:5007063","phenotype":{"types":[{"id":"MP:0002116","label":"abnormal craniofacial bone morphology"}]}},{"entity":"ClinVarVariant:188088","phenotype":{"types":[{"id":"HP:0002669","label":"Osteosarcoma"}]}},{"entity":"ClinVarVariant:196277","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:38289","phenotype":{"types":[{"id":"HP:0002789","label":"Tachypnea"}]}},{"entity":"ClinVarVariant:16741","phenotype":{"types":[{"id":"HP:0000153","label":"Abnormality of the mouth"}]}},{"entity":"ClinVarVariant:10654","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"ClinVarVariant:5508","phenotype":{"types":[{"id":"HP:0000882","label":"Hypoplastic scapulae"}]}},{"entity":"ClinVarVariant:211503","phenotype":{"types":[{"id":"HP:0001195","label":"Single umbilical artery"}]}},{"entity":"ClinVarVariant:53915","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:3756","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:42443","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"MGI:3798768","phenotype":{"types":[{"id":"MP:0005076","label":"abnormal cell differentiation"}]}},{"entity":"ClinVarVariant:101503","phenotype":{"types":[{"id":"HP:0010752","label":"Cleft mandible"}]}},{"entity":"ClinVarVariant:64997","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:1539","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:101108","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"ClinVarVariant:43202","phenotype":{"types":[{"id":"HP:0000360","label":"Tinnitus"}]}},{"entity":"ClinVarVariant:5943","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:24508","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:38311","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:1128","phenotype":{"types":[{"id":"HP:0000895","label":"Lateral clavicle hook"}]}},{"entity":"MGI:2388126","phenotype":{"types":[{"id":"MP:0002113","label":"abnormal skeleton development"}]}},{"entity":"ClinVarVariant:96576","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"ClinVarVariant:53236","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:193747","phenotype":{"types":[{"id":"HP:0001256","label":"Intellectual disability, mild"}]}},{"entity":"ClinVarVariant:126412","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:94109","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"dbSNP:rs41666553","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:31217","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:54003","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:25350","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"ClinVarVariant:198365","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"ClinVarVariant:24676","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"ClinVarVariant:94210","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:101296","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"DOID:11726","phenotype":{"types":[{"id":"HP:0001638","label":"Cardiomyopathy"}]}},{"entity":"FlyBase:FBal0118076","phenotype":{"types":[{"id":"FBcv:0000394","label":"circadian rhythm defective"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00009186-WBRNAi00045737","phenotype":{"types":[{"id":"WBPhenotype:0000640","label":"egg laying variant"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003186-WBRNAi00085575","phenotype":{"types":[{"id":"WBPhenotype:0000291","label":"no oocytes"}]}},{"entity":"ClinVarVariant:24755","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:11836","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:158924","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:67977","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:55823","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050523-1-ZDB-MRPHLNO-080703-4","phenotype":{"types":[{"id":"ZP:0007823","label":"abnormal(ly) increased width floor plate rhombomere region"}]}},{"entity":"ClinVarVariant:65018","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:67936","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:188997","phenotype":{"types":[{"id":"HP:0001954","label":"Episodic fever"}]}},{"entity":"ClinVarVariant:190776","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:50061","phenotype":{"types":[{"id":"HP:0000269","label":"Prominent occiput"}]}},{"entity":"ClinVarVariant:13674","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-030131-180-ZDB-MRPHLNO-110715-2","phenotype":{"types":[{"id":"GO:0035188PHENOTYPE","label":"hatching phenotype"}]}},{"entity":"ClinVarVariant:6639","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"FlyBase:FBal0205870","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:54073","phenotype":{"types":[{"id":"HP:0000966","label":"Hypohidrosis"}]}},{"entity":"MGI:3588578","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:50112","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"ClinVarVariant:11860","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008688-WBRNAi00080126","phenotype":{"types":[{"id":"ZP:0000676","label":"abnormal(ly) increased rate cell proliferation"}]}},{"entity":"ClinVarVariant:18086","phenotype":{"types":[{"id":"HP:0002884","label":"Hepatoblastoma"}]}},{"entity":"ClinVarVariant:7516","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"ClinVarVariant:94475","phenotype":{"types":[{"id":"HP:0002948","label":"Vertebral fusion"}]}},{"entity":"dbSNP:rs12793173","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:1532","phenotype":{"types":[{"id":"HP:0010980","label":"Hyperlipoproteinemia"}]}},{"entity":"ClinVarVariant:158567","phenotype":{"types":[{"id":"HP:0009836","label":"Broad distal phalanx of finger"}]}},{"entity":"ClinVarVariant:188263","phenotype":{"types":[{"id":"HP:0002321","label":"Vertigo"}]}},{"entity":"ClinVarVariant:141451","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00015583-WBRNAi00077058","phenotype":{"types":[{"id":"WBPhenotype:0000012","label":"dauer constitutive"}]}},{"entity":"ClinVarVariant:208075","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"MGI:2156546","phenotype":{"types":[{"id":"MP:0005597","label":"decreased susceptibility to type I hypersensitivity reaction"}]}},{"entity":"MGI:5285080","phenotype":{"types":[{"id":"MP:0013209","label":"abnormal motile cilium physiology"}]}},{"entity":"ClinVarVariant:38281","phenotype":{"types":[{"id":"HP:0011131","label":"Perianal rash"}]}},{"entity":"ClinVarVariant:53127","phenotype":{"types":[{"id":"HP:0006696","label":"Polymorphic and polytopic ventricular extrasystoles"}]}},{"entity":"MGI:3822156","phenotype":{"types":[{"id":"MP:0000281","label":"abnormal interventricular septum morphology"}]}},{"entity":"ClinVarVariant:49660","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:39711","phenotype":{"types":[{"id":"HP:0001171","label":"Split hand"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003947-WBRNAi00085486","phenotype":{"types":[{"id":"WBPhenotype:0001950","label":"diplotene region organization variant"}]}},{"entity":"ClinVarVariant:127405","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:43995","phenotype":{"types":[{"id":"HP:0001678","label":"Atrioventricular block"}]}},{"entity":"ClinVarVariant:188886","phenotype":{"types":[{"id":"HP:0001878","label":"Hemolytic anemia"}]}},{"entity":"ClinVarVariant:101248","phenotype":{"types":[{"id":"HP:0100627","label":"Displacement of the external urethral meatus"}]}},{"entity":"ClinVarVariant:17360","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006375-WBRNAi00097656","phenotype":{"types":[{"id":"ZP:0004962","label":"abnormal(ly) increased rate apoptotic process"}]}},{"entity":"ClinVarVariant:38942","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:8482","phenotype":{"types":[{"id":"HP:0001332","label":"Dystonia"}]}},{"entity":"ClinVarVariant:12497","phenotype":{"types":[{"id":"HP:0011039","label":"Abnormality of the helix"}]}},{"entity":"ClinVarVariant:1480","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:189710","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:690","phenotype":{"types":[{"id":"HP:0000914","label":"Shield chest"}]}},{"entity":"ClinVarVariant:136123","phenotype":{"types":[{"id":"HP:0000980","label":"Pallor"}]}},{"entity":"MGI:3040471","phenotype":{"types":[{"id":"HP:0011111","label":"Abnormality of immune serum protein physiology"}]}},{"entity":"ClinVarVariant:210716","phenotype":{"types":[{"id":"HP:0001231","label":"Abnormality of the fingernails"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001967-WBRNAi00070035","phenotype":{"types":[{"id":"WBPhenotype:0000696","label":"everted vulva"}]}},{"entity":"ClinVarVariant:53210","phenotype":{"types":[{"id":"HP:0006536","label":"Obstructive lung disease"}]}},{"entity":"ClinVarVariant:53246","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:24716","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:212636","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:10118","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"ClinVarVariant:17484","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:202177","phenotype":{"types":[{"id":"HP:0010780","label":"Hyperacusis"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050419-261-ZDB-MRPHLNO-130117-3","phenotype":{"types":[{"id":"ZP:0002516","label":"abnormal(ly) cystic pronephric glomerulus"}]}},{"entity":"ClinVarVariant:66036","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"dbSNP:rs586716","phenotype":{"types":[{"id":"HP:0003418","label":"Back pain"}]}},{"entity":"ClinVarVariant:101414","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:49414","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"ClinVarVariant:166862","phenotype":{"types":[{"id":"HP:0000689","label":"Dental malocclusion"}]}},{"entity":"ClinVarVariant:41344","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"MGI:5431878","phenotype":{"types":[{"id":"HP:0012373","label":"Abnormal eye physiology"}]}},{"entity":"ClinVarVariant:155889","phenotype":{"types":[{"id":"HP:0001950","label":"Respiratory alkalosis"}]}},{"entity":"ClinVarVariant:1743","phenotype":{"types":[{"id":"HP:0200118","label":"Malabsorption of Vitamin B12"}]}},{"entity":"ClinVarVariant:65028","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:24275","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"ClinVarVariant:53680","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:92800","phenotype":{"types":[{"id":"HP:0000219","label":"Thin upper lip vermilion"}]}},{"entity":"ClinVarVariant:13997","phenotype":{"types":[{"id":"HP:0004429","label":"Recurrent viral infections"}]}},{"entity":"ClinVarVariant:54064","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"MGI:1857348","phenotype":{"types":[{"id":"HP:0100495","label":"Mastocytosis"}]}},{"entity":"ClinVarVariant:40512","phenotype":{"types":[{"id":"HP:0000276","label":"Long face"}]}},{"entity":"FlyBase:FBal0095694","phenotype":{"types":[{"id":"FBbt:00004200PHENOTYPE","label":"retina phenotype"}]}},{"entity":"MGI:2677682","phenotype":{"types":[{"id":"MP:0002813","label":"microcytosis"}]}},{"entity":"dbSNP:rs7045640","phenotype":{"types":[{"id":"HP:0001489","label":"Posterior vitreous detachment"}]}},{"entity":"ClinVarVariant:5094","phenotype":{"types":[{"id":"HP:0002757","label":"Recurrent fractures"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002064-WBRNAi00063098","phenotype":{"types":[{"id":"WBPhenotype:0000291","label":"no oocytes"}]}},{"entity":"ClinVarVariant:11134","phenotype":{"types":[{"id":"HP:0001891","label":"Iron deficiency anemia"}]}},{"entity":"ClinVarVariant:189284","phenotype":{"types":[{"id":"HP:0008572","label":"External ear malformation"}]}},{"entity":"MGI:3057163","phenotype":{"types":[{"id":"HP:0001882","label":"Leukopenia"}]}},{"entity":"MGI:3846101","phenotype":{"types":[{"id":"MP:0002874","label":"decreased hemoglobin content"}]}},{"entity":"ClinVarVariant:12051","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:56263","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"AQTL:11570","phenotype":{"types":[{"id":"AQTLTrait:224","label":"Small intestinal Escherichia coli F18 receptor"}]}},{"entity":"ClinVarVariant:40551","phenotype":{"types":[{"id":"HP:0010541","label":"Cutis gyrata of scalp"}]}},{"entity":"ClinVarVariant:54031","phenotype":{"types":[{"id":"HP:0005948","label":"Cystic lung disease"}]}},{"entity":"ClinVarVariant:42343","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"MGI:3512077","phenotype":{"types":[{"id":"MP:0000750","label":"abnormal muscle regeneration"}]}},{"entity":"ClinVarVariant:50982","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"MGI:2448247","phenotype":{"types":[{"id":"MP:0001176","label":"abnormal lung development"}]}},{"entity":"ClinVarVariant:53871","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004078-WBRNAi00091973","phenotype":{"types":[{"id":"ZP:0000305","label":"abnormal(ly) arrested embryo development"}]}},{"entity":"FlyBase:FBal0200222","phenotype":{"types":[{"id":"FBbt:00005149PHENOTYPE","label":"ganglion mother cell phenotype"}]}},{"entity":"ClinVarVariant:216429","phenotype":{"types":[{"id":"HP:0100280","label":"Crohn's disease"}]}},{"entity":"ClinVarVariant:2392","phenotype":{"types":[{"id":"HP:0003218","label":"Oroticaciduria"}]}},{"entity":"ClinVarVariant:142966","phenotype":{"types":[{"id":"HP:0000777","label":"Abnormality of the thymus"}]}},{"entity":"MGI:3624543","phenotype":{"types":[{"id":"MP:0000951","label":"sporadic seizures"}]}},{"entity":"ClinVarVariant:133608","phenotype":{"types":[{"id":"HP:0002344","label":"Progressive neurologic deterioration"}]}},{"entity":"ClinVarVariant:211626","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:9656","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:25215","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:10572","phenotype":{"types":[{"id":"HP:0005186","label":"Synovial hypertrophy"}]}},{"entity":"MGI:3722688","phenotype":{"types":[{"id":"HP:0003022","label":"Hypoplasia of the ulna"}]}},{"entity":"ClinVarVariant:93129","phenotype":{"types":[{"id":"HP:0002371","label":"Loss of speech"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004806-WBRNAi00036044","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"MGI:2386742","phenotype":{"types":[{"id":"HP:0001719","label":"Double outlet right ventricle"}]}},{"entity":"ClinVarVariant:12534","phenotype":{"types":[{"id":"HP:0002659","label":"Increased susceptibility to fractures"}]}},{"entity":"ClinVarVariant:53491","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"WormBase:WBVar00087758","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:100772","phenotype":{"types":[{"id":"HP:0000174","label":"Abnormality of the palate"}]}},{"entity":"FlyBase:FBal0269186","phenotype":{"types":[{"id":"FBbt:00004646PHENOTYPE","label":"tarsal segment phenotype"}]}},{"entity":"ClinVarVariant:209167","phenotype":{"types":[{"id":"HP:0000666","label":"Horizontal nystagmus"}]}},{"entity":"AQTL:29399","phenotype":{"types":[{"id":"AQTLTrait:1085","label":"Degree of Spotting"}]}},{"entity":"ZFIN:ZDB-ALT-090611-2","phenotype":{"types":[{"id":"GO:0045765PHENOTYPE","label":"regulation of angiogenesis phenotype"}]}},{"entity":"ClinVarVariant:36053","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:101388","phenotype":{"types":[{"id":"HP:0009906","label":"Aplasia/Hypoplasia of the earlobes"}]}},{"entity":"MGI:3605473","phenotype":{"types":[{"id":"MP:0004167","label":"abnormal cingulate gyrus morphology"}]}},{"entity":"MGI:4433578","phenotype":{"types":[{"id":"MP:0004527","label":"abnormal outer hair cell stereociliary bundle morphology"}]}},{"entity":"ClinVarVariant:2324","phenotype":{"types":[{"id":"HP:0001315","label":"Reduced tendon reflexes"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-061103-265-ZDB-MRPHLNO-140606-7","phenotype":{"types":[{"id":"ZP:0004552","label":"abnormal(ly) bilateral symmetry heart tube"}]}},{"entity":"ClinVarVariant:181833","phenotype":{"types":[{"id":"HP:0100777","label":"Exostoses"}]}},{"entity":"ClinVarVariant:93455","phenotype":{"types":[{"id":"HP:0000939","label":"Osteoporosis"}]}},{"entity":"MGI:3817754","phenotype":{"types":[{"id":"HP:0000859","label":"Hyperaldosteronism"}]}},{"entity":"ClinVarVariant:211657","phenotype":{"types":[{"id":"HP:0000776","label":"Congenital diaphragmatic hernia"}]}},{"entity":"ClinVarVariant:35972","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:4674","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"ClinVarVariant:8953","phenotype":{"types":[{"id":"HP:0006380","label":"Knee flexion contracture"}]}},{"entity":"FlyBase:FBal0221490","phenotype":{"types":[{"id":"FBbt:00004483PHENOTYPE","label":"Drosophila ptilinum phenotype"}]}},{"entity":"FlyBase:FBal0050220","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"FlyBase:FBal0200679","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"MGI:2178387","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:41120","phenotype":{"types":[{"id":"HP:0100612","label":"Odontogenic neoplasm"}]}},{"entity":"ClinVarVariant:13723","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:161333","phenotype":{"types":[{"id":"HP:0001038","label":"Warfarin-induced skin necrosis"}]}},{"entity":"ClinVarVariant:6099","phenotype":{"types":[{"id":"HP:0003312","label":"Abnormal form of the vertebral bodies"}]}},{"entity":"ClinVarVariant:41180","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:9430","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:99932","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:36072","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:1987","phenotype":{"types":[{"id":"HP:0000057","label":"obsolete Clitoromegaly"}]}},{"entity":"ClinVarVariant:158899","phenotype":{"types":[{"id":"HP:0003324","label":"Generalized muscle weakness"}]}},{"entity":"ZFIN:ZDB-ALT-041008-4","phenotype":{"types":[{"id":"ZP:0000407","label":"abnormal(ly) decreased width head"}]}},{"entity":"ClinVarVariant:7292","phenotype":{"types":[{"id":"HP:0001053","label":"Hypopigmented skin patches"}]}},{"entity":"ClinVarVariant:67378","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:36284","phenotype":{"types":[{"id":"HP:0000832","label":"Primary hypothyroidism"}]}},{"entity":"ClinVarVariant:194096","phenotype":{"types":[{"id":"HP:0000572","label":"Visual loss"}]}},{"entity":"ClinVarVariant:197503","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"AQTL:15249","phenotype":{"types":[{"id":"AQTLTrait:1027","label":"Marbling score"}]}},{"entity":"ClinVarVariant:49120","phenotype":{"types":[{"id":"HP:0008696","label":"Renal hamartoma"}]}},{"entity":"ClinVarVariant:12335","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:7979","phenotype":{"types":[{"id":"HP:0000400","label":"Macrotia"}]}},{"entity":"ClinVarVariant:49153","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:53913","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:133623","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ZFIN:ZDB-ALT-100723-4","phenotype":{"types":[{"id":"ZP:0007051","label":"abnormal(ly) dilated melanocyte"}]}},{"entity":"ClinVarVariant:88731","phenotype":{"types":[{"id":"HP:0012557","label":"EEG with centrotemporal focal spike waves"}]}},{"entity":"ClinVarVariant:49298","phenotype":{"types":[{"id":"HP:0009727","label":"Achromatic retinal patches"}]}},{"entity":"dbSNP:rs136851063","phenotype":{"types":[{"id":"AQTLTrait:1327","label":"Milk odd-chain fatty acid percentage"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00012059-WBRNAi00009225","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:30201","phenotype":{"types":[{"id":"HP:0000453","label":"Choanal atresia"}]}},{"entity":"MGI:2665856","phenotype":{"types":[{"id":"MP:0008190","label":"decreased transitional stage B cell number"}]}},{"entity":"ClinVarVariant:7165","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"ClinVarVariant:4078","phenotype":{"types":[{"id":"HP:0000529","label":"Progressive visual loss"}]}},{"entity":"ClinVarVariant:204238","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:53925","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"MGI:1860953","phenotype":{"types":[{"id":"MP:0008470","label":"abnormal spleen B cell follicle morphology"}]}},{"entity":"ClinVarVariant:53256","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"MGI:2386947","phenotype":{"types":[{"id":"HP:0010831","label":"Impaired proprioception"}]}},{"entity":"ClinVarVariant:158721","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:39468","phenotype":{"types":[{"id":"HP:0001845","label":"Overlapping toe"}]}},{"entity":"ClinVarVariant:53178","phenotype":{"types":[{"id":"HP:0004395","label":"Malnutrition"}]}},{"entity":"ClinVarVariant:158944","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00020820-WBRNAi00064595","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:53499","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:53943","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:209145","phenotype":{"types":[{"id":"HP:0006101","label":"Finger syndactyly"}]}},{"entity":"WormBase:WBVar00275350","phenotype":{"types":[{"id":"WBPhenotype:0000135","label":"gene expression level high"}]}},{"entity":"ClinVarVariant:53620","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:136034","phenotype":{"types":[{"id":"HP:0001587","label":"Primary ovarian failure"}]}},{"entity":"ClinVarVariant:10164","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:211738","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"ClinVarVariant:10083","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:211636","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:8570","phenotype":{"types":[{"id":"HP:0011423","label":"Hyperchloremia"}]}},{"entity":"ClinVarVariant:46449","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:93762","phenotype":{"types":[{"id":"HP:0000668","label":"Hypodontia"}]}},{"entity":"FlyBase:FBal0210265","phenotype":{"types":[{"id":"FBbt:00005169PHENOTYPE","label":"Drosophila trichogen cell phenotype"}]}},{"entity":"ClinVarVariant:38990","phenotype":{"types":[{"id":"HP:0003458","label":"EMG: myopathic abnormalities"}]}},{"entity":"ClinVarVariant:216803","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:3602","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:5712","phenotype":{"types":[{"id":"HP:0001611","label":"Nasal speech"}]}},{"entity":"MGI:4459725","phenotype":{"types":[{"id":"MP:0002044","label":"increased colonic adenoma incidence"}]}},{"entity":"ClinVarVariant:41109","phenotype":{"types":[{"id":"HP:0010297","label":"Bifid tongue"}]}},{"entity":"ClinVarVariant:101374","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"MGI:1857312","phenotype":{"types":[{"id":"MP:0001666","label":"abnormal intestinal absorption"}]}},{"entity":"dbSNP:rs4149584","phenotype":{"types":[{"id":"HP:0002321","label":"Vertigo"}]}},{"entity":"ClinVarVariant:5746","phenotype":{"types":[{"id":"HP:0001622","label":"Premature birth"}]}},{"entity":"ClinVarVariant:53799","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"ClinVarVariant:50176","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:155800","phenotype":{"types":[{"id":"HP:0011034","label":"Amyloidosis"}]}},{"entity":"ClinVarVariant:36063","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:100773","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"ClinVarVariant:6866","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"MGI:3527932","phenotype":{"types":[{"id":"MP:0002705","label":"dilated renal tubules"}]}},{"entity":"ClinVarVariant:9137","phenotype":{"types":[{"id":"HP:0003124","label":"Hypercholesterolemia"}]}},{"entity":"ClinVarVariant:181716","phenotype":{"types":[{"id":"HP:0100542","label":"Abnormal localization of kidney"}]}},{"entity":"ClinVarVariant:189941","phenotype":{"types":[{"id":"HP:0005484","label":"Postnatal microcephaly"}]}},{"entity":"ClinVarVariant:132825","phenotype":{"types":[{"id":"HP:0001660","label":"Truncus arteriosus"}]}},{"entity":"ClinVarVariant:133530","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:14519","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:13072","phenotype":{"types":[{"id":"HP:0009824","label":"Upper limb undergrowth"}]}},{"entity":"ClinVarVariant:156361","phenotype":{"types":[{"id":"HP:0000062","label":"Ambiguous genitalia"}]}},{"entity":"ClinVarVariant:13783","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:7623","phenotype":{"types":[{"id":"HP:0000772","label":"Abnormality of the ribs"}]}},{"entity":"MGI:3821974","phenotype":{"types":[{"id":"MP:0001463","label":"abnormal spatial learning"}]}},{"entity":"ClinVarVariant:120296","phenotype":{"types":[{"id":"HP:0001010","label":"Hypopigmentation of the skin"}]}},{"entity":"ClinVarVariant:127306","phenotype":{"types":[{"id":"HP:0008256","label":"Adrenocortical adenoma"}]}},{"entity":"ClinVarVariant:12873","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:49281","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:211620","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"MGI:2384535","phenotype":{"types":[{"id":"MP:0001442","label":"decreased grooming behavior"}]}},{"entity":"ClinVarVariant:31180","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"ClinVarVariant:17088","phenotype":{"types":[{"id":"HP:0100279","label":"Ulcerative colitis"}]}},{"entity":"MGI:2653910","phenotype":{"types":[{"id":"MP:0008501","label":"increased IgG2b level"}]}},{"entity":"ClinVarVariant:1545","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:53266","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:50949","phenotype":{"types":[{"id":"HP:0000817","label":"Poor eye contact"}]}},{"entity":"FlyBase:FBal0156488","phenotype":{"types":[{"id":"GO:0042600PHENOTYPE","label":"chorion phenotype"}]}},{"entity":"ClinVarVariant:41058","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:101132","phenotype":{"types":[{"id":"HP:0000490","label":"Deeply set eye"}]}},{"entity":"ClinVarVariant:127247","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:53389","phenotype":{"types":[{"id":"HP:0000855","label":"Insulin resistance"}]}},{"entity":"ClinVarVariant:143808","phenotype":{"types":[{"id":"HP:0002376","label":"Developmental regression"}]}},{"entity":"ClinVarVariant:53545","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"ClinVarVariant:65904","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"_:genid1972746","phenotype":{"types":[{"id":"ZP:0001671","label":"abnormal(ly) disrupted locomotory behavior"}]}},{"entity":"ClinVarVariant:6040","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"MGI:5527336","phenotype":{"types":[{"id":"MP:0010639","label":"altered tumor pathology"}]}},{"entity":"ClinVarVariant:102556","phenotype":{"types":[{"id":"HP:0000709","label":"Psychosis"}]}},{"entity":"FlyBase:FBal0205295","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:21350","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"ClinVarVariant:54074","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"MGI:1861186","phenotype":{"types":[{"id":"MP:0004473","label":"absent nasal bone"}]}},{"entity":"ClinVarVariant:52388","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:42069","phenotype":{"types":[{"id":"HP:0002720","label":"IgA deficiency"}]}},{"entity":"ClinVarVariant:68059","phenotype":{"types":[{"id":"HP:0011704","label":"Sick sinus syndrome"}]}},{"entity":"MGI:2153356","phenotype":{"types":[{"id":"HP:0003687","label":"Centrally nucleated skeletal muscle fibers"}]}},{"entity":"ClinVarVariant:15624","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:197669","phenotype":{"types":[{"id":"HP:0010783","label":"Erythema"}]}},{"entity":"ClinVarVariant:7256","phenotype":{"types":[{"id":"HP:0002619","label":"Varicose veins"}]}},{"entity":"ClinVarVariant:36838","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:21094","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:53431","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"AQTL:24319","phenotype":{"types":[{"id":"AQTLTrait:1090","label":"Longissimus muscle area"}]}},{"entity":"ClinVarVariant:215458","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"ClinVarVariant:158744","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"ClinVarVariant:39713","phenotype":{"types":[{"id":"HP:0000194","label":"Open mouth"}]}},{"entity":"ClinVarVariant:36073","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:165770","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:4321","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:4179","phenotype":{"types":[{"id":"HP:0001332","label":"Dystonia"}]}},{"entity":"MGI:4435548","phenotype":{"types":[{"id":"MP:0002418","label":"increased susceptibility to viral infection"}]}},{"entity":"ClinVarVariant:50071","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:40493","phenotype":{"types":[{"id":"HP:0000824","label":"Growth hormone deficiency"}]}},{"entity":"ClinVarVariant:9192","phenotype":{"types":[{"id":"HP:0012307","label":"Spatulate ribs"}]}},{"entity":"ClinVarVariant:49601","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:31911","phenotype":{"types":[{"id":"HP:0000384","label":"Preauricular skin tag"}]}},{"entity":"ClinVarVariant:9767","phenotype":{"types":[{"id":"HP:0003236","label":"Elevated serum creatine phosphokinase"}]}},{"entity":"ClinVarVariant:66505","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:1578","phenotype":{"types":[{"id":"HP:0002487","label":"Hyperkinesis"}]}},{"entity":"ClinVarVariant:10048","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004397-WBRNAi00089816","phenotype":{"types":[{"id":"WBPhenotype:0000583","label":"dumpy"}]}},{"entity":"ClinVarVariant:10166","phenotype":{"types":[{"id":"HP:0005268","label":"Spontaneous abortion"}]}},{"entity":"ClinVarVariant:8653","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:17939","phenotype":{"types":[{"id":"HP:0010517","label":"Ectopic thymus tissue"}]}},{"entity":"MGI:1856276","phenotype":{"types":[{"id":"MP:0000914","label":"exencephaly"}]}},{"entity":"ClinVarVariant:1740","phenotype":{"types":[{"id":"HP:0001511","label":"Intrauterine growth retardation"}]}},{"entity":"ClinVarVariant:93124","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:53310","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:91640","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"NCBIGene:100126595","phenotype":{"types":[{"id":"HP:0100771","label":"Hypoperistalsis"}]}},{"entity":"ClinVarVariant:11715","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"MGI:2447334","phenotype":{"types":[{"id":"HP:0012757","label":"Abnormal neuron morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008149-WBRNAi00008529","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:49227","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:143544","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"dbSNP:rs81339346","phenotype":{"types":[{"id":"AQTLTrait:1483","label":"Red blood cell count"}]}},{"entity":"ClinVarVariant:127155","phenotype":{"types":[{"id":"HP:0000622","label":"Blurred vision"}]}},{"entity":"ClinVarVariant:102444","phenotype":{"types":[{"id":"HP:0000561","label":"Absent eyelashes"}]}},{"entity":"MGI:1857139","phenotype":{"types":[{"id":"MP:0000528","label":"delayed kidney development"}]}},{"entity":"ClinVarVariant:158964","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:49611","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:17384","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:216211","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"MGI:3758075","phenotype":{"types":[{"id":"MP:0000822","label":"abnormal brain ventricle morphology"}]}},{"entity":"ClinVarVariant:29712","phenotype":{"types":[{"id":"HP:0002841","label":"Recurrent fungal infections"}]}},{"entity":"MGI:1857314","phenotype":{"types":[{"id":"MP:0011093","label":"embryonic lethality at implantation, complete penetrance"}]}},{"entity":"ClinVarVariant:217430","phenotype":{"types":[{"id":"HP:0001820","label":"Leukonychia"}]}},{"entity":"MGI:4421830","phenotype":{"types":[{"id":"HP:0012864","label":"Abnormal sperm morphology"}]}},{"entity":"ClinVarVariant:198077","phenotype":{"types":[{"id":"HP:0001638","label":"Cardiomyopathy"}]}},{"entity":"MGI:1857229","phenotype":{"types":[{"id":"MP:0000260","label":"abnormal angiogenesis"}]}},{"entity":"MGI:3806024","phenotype":{"types":[{"id":"HP:0011273","label":"Anisocytosis"}]}},{"entity":"ClinVarVariant:50907","phenotype":{"types":[{"id":"HP:0001043","label":"Prominent scalp veins"}]}},{"entity":"ClinVarVariant:3851","phenotype":{"types":[{"id":"HP:0000787","label":"Nephrolithiasis"}]}},{"entity":"ClinVarVariant:40599","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:9597","phenotype":{"types":[{"id":"HP:0001700","label":"Myocardial necrosis"}]}},{"entity":"ClinVarVariant:39524","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:16287","phenotype":{"types":[{"id":"HP:0001363","label":"Craniosynostosis"}]}},{"entity":"MGI:3663386","phenotype":{"types":[{"id":"MP:0005449","label":"abnormal food intake"}]}},{"entity":"ClinVarVariant:12345","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:11012","phenotype":{"types":[{"id":"HP:0001298","label":"Encephalopathy"}]}},{"entity":"ClinVarVariant:53276","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:53901","phenotype":{"types":[{"id":"HP:0003453","label":"Antineutrophil antibody positivity"}]}},{"entity":"MGI:3811603","phenotype":{"types":[{"id":"HP:0003097","label":"Short femur"}]}},{"entity":"ClinVarVariant:6925","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:11788","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ClinVarVariant:54083","phenotype":{"types":[{"id":"HP:0006536","label":"Obstructive lung disease"}]}},{"entity":"ClinVarVariant:11722","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:210318","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006996-WBRNAi00007928","phenotype":{"types":[{"id":"WBPhenotype:0001168","label":"pseudocleavage absent early emb"}]}},{"entity":"ClinVarVariant:182830","phenotype":{"types":[{"id":"HP:0100587","label":"Abnormality of the preputium"}]}},{"entity":"ClinVarVariant:6165","phenotype":{"types":[{"id":"HP:0006789","label":"Mitochondrial encephalopathy"}]}},{"entity":"dbSNP:rs7903146","phenotype":{"types":[{"id":"HP:0100710","label":"Impulsivity"}]}},{"entity":"ClinVarVariant:24926","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:65048","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:6822","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"MGI:3046573","phenotype":{"types":[{"id":"MP:0011085","label":"postnatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:21278","phenotype":{"types":[{"id":"HP:0001222","label":"Spatulate thumbs"}]}},{"entity":"ClinVarVariant:56227","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:155948","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"dbSNP:rs1027643","phenotype":{"types":[{"id":"HP:0000526","label":"Aniridia"}]}},{"entity":"_:genid1976410","phenotype":{"types":[{"id":"ZP:0000868","label":"abnormal(ly) disrupted convergent extension involved in gastrulation"}]}},{"entity":"ClinVarVariant:8267","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"ClinVarVariant:189559","phenotype":{"types":[{"id":"HP:0011097","label":"Epileptic spasms"}]}},{"entity":"ClinVarVariant:2676","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:3621117","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:159096","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-050306-15-ZDB-MRPHLNO-100618-3","phenotype":{"types":[{"id":"GO:0060538PHENOTYPE","label":"skeletal muscle organ development phenotype"}]}},{"entity":"ClinVarVariant:211646","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:189579","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"ClinVarVariant:126807","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:14052","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"MGI:5563785","phenotype":{"types":[{"id":"MP:0009347","label":"increased trabecular bone thickness"}]}},{"entity":"ClinVarVariant:36083","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:195458","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:4300","phenotype":{"types":[{"id":"HP:0003540","label":"Impaired platelet aggregation"}]}},{"entity":"ClinVarVariant:194115","phenotype":{"types":[{"id":"HP:0000962","label":"Hyperkeratosis"}]}},{"entity":"ClinVarVariant:67967","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:16839","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"MGI:4459093","phenotype":{"types":[{"id":"HP:0010831","label":"Impaired proprioception"}]}},{"entity":"ClinVarVariant:209134","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:178847","phenotype":{"types":[{"id":"HP:0001742","label":"Nasal obstruction"}]}},{"entity":"ClinVarVariant:68699","phenotype":{"types":[{"id":"HP:0100530","label":"Abnormality of calcium-phosphate metabolism"}]}},{"entity":"MGI:1856217","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:189359","phenotype":{"types":[{"id":"HP:0000709","label":"Psychosis"}]}},{"entity":"MGI:3510782","phenotype":{"types":[{"id":"MP:0008699","label":"increased interleukin-4 secretion"}]}},{"entity":"MGI:2447199","phenotype":{"types":[{"id":"MP:0000932","label":"absent notochord"}]}},{"entity":"FlyBase:FBal0207596","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:42079","phenotype":{"types":[{"id":"HP:0002720","label":"IgA deficiency"}]}},{"entity":"ClinVarVariant:143802","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:7622","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"MGI:5295747","phenotype":{"types":[{"id":"HP:0003292","label":"Decreased serum leptin"}]}},{"entity":"ClinVarVariant:884","phenotype":{"types":[{"id":"HP:0002318","label":"Cervical myelopathy"}]}},{"entity":"ClinVarVariant:204096","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"ClinVarVariant:1389","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:94230","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:49530","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:30696","phenotype":{"types":[{"id":"HP:0000256","label":"Macrocephaly"}]}},{"entity":"WormBase:WBVar00146313","phenotype":{"types":[{"id":"WBPhenotype:0000962","label":"level of transgene expression variant"}]}},{"entity":"ClinVarVariant:53294","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ClinVarVariant:53935","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"MGI:3757964","phenotype":{"types":[{"id":"HP:0001719","label":"Double outlet right ventricle"}]}},{"entity":"ClinVarVariant:53738","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:193517","phenotype":{"types":[{"id":"HP:0000992","label":"Cutaneous photosensitivity"}]}},{"entity":"MGI:1857930","phenotype":{"types":[{"id":"HP:0011804","label":"Abnormality of muscle physiology"}]}},{"entity":"ClinVarVariant:68711","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:158339","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:6718","phenotype":{"types":[{"id":"HP:0001908","label":"Hypoplastic anemia"}]}},{"entity":"ClinVarVariant:94139","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"ClinVarVariant:45115","phenotype":{"types":[{"id":"HP:0002859","label":"Rhabdomyosarcoma"}]}},{"entity":"MGI:2678305","phenotype":{"types":[{"id":"MP:0002169","label":"no abnormal phenotype detected"}]}},{"entity":"ClinVarVariant:158974","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:9236","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000067-WBRNAi00085673","phenotype":{"types":[{"id":"WBPhenotype:0001260","label":"oocyte morphology variant"}]}},{"entity":"ClinVarVariant:4262","phenotype":{"types":[{"id":"HP:0005177","label":"Premature arteriosclerosis"}]}},{"entity":"ClinVarVariant:42327","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"dbSNP:rs6729815","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"MGI:3840238","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:65058","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:36091","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:7360","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"ClinVarVariant:5225","phenotype":{"types":[{"id":"HP:0011003","label":"Severe Myopia"}]}},{"entity":"ClinVarVariant:65166","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"MGI:3832033","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"ClinVarVariant:10761","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:210456","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003401-WBRNAi00085349","phenotype":{"types":[{"id":"WBPhenotype:0001944","label":"oocyte number decreased"}]}},{"entity":"ClinVarVariant:42089","phenotype":{"types":[{"id":"HP:0002720","label":"IgA deficiency"}]}},{"entity":"FlyBase:FBal0119169","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:186362","phenotype":{"types":[{"id":"HP:0001908","label":"Hypoplastic anemia"}]}},{"entity":"ClinVarVariant:127417","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:39785","phenotype":{"types":[{"id":"HP:0000772","label":"Abnormality of the ribs"}]}},{"entity":"MGI:1857212","phenotype":{"types":[{"id":"MP:0005458","label":"increased percent body fat/body weight"}]}},{"entity":"ClinVarVariant:143525","phenotype":{"types":[{"id":"HP:0000729","label":"Autistic behavior"}]}},{"entity":"ClinVarVariant:101294","phenotype":{"types":[{"id":"HP:0100689","label":"Decreased corneal thickness"}]}},{"entity":"ClinVarVariant:167361","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"ClinVarVariant:16342","phenotype":{"types":[{"id":"HP:0003811","label":"Neonatal death"}]}},{"entity":"MGI:1857722","phenotype":{"types":[{"id":"MP:0012165","label":"absent neural folds"}]}},{"entity":"ClinVarVariant:159921","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:12023","phenotype":{"types":[{"id":"HP:0010978","label":"Abnormality of immune system physiology"}]}},{"entity":"ZFIN:ZDB-ALT-040929-4","phenotype":{"types":[{"id":"ZP:0000043","label":"abnormal(ly) decreased size eye"}]}},{"entity":"ClinVarVariant:10118","phenotype":{"types":[{"id":"HP:0005542","label":"Prolonged whole-blood clotting time"}]}},{"entity":"MGI:2176049","phenotype":{"types":[{"id":"HP:0002414","label":"Spina bifida"}]}},{"entity":"ClinVarVariant:53923","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:49631","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:36093","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:35890","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"dbSNP:rs109529219","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:8875","phenotype":{"types":[{"id":"HP:0009773","label":"Symphalangism affecting the phalanges of the hand"}]}},{"entity":"MGI:5548830","phenotype":{"types":[{"id":"MP:0010123","label":"increased bone mineral content"}]}},{"entity":"ClinVarVariant:141944","phenotype":{"types":[{"id":"HP:0005374","label":"Cellular immunodeficiency"}]}},{"entity":"ClinVarVariant:40068","phenotype":{"types":[{"id":"HP:0000105","label":"Enlarged kidneys"}]}},{"entity":"ClinVarVariant:7427","phenotype":{"types":[{"id":"HP:0100015","label":"Stahl ear"}]}},{"entity":"MGI:1931521","phenotype":{"types":[{"id":"MP:0005296","label":"abnormal humerus morphology"}]}},{"entity":"ClinVarVariant:10288","phenotype":{"types":[{"id":"HP:0012062","label":"Bone cyst"}]}},{"entity":"FlyBase:FBal0178561","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"MGI:3623277","phenotype":{"types":[{"id":"MP:0003944","label":"abnormal T cell subpopulation ratio"}]}},{"entity":"ClinVarVariant:217280","phenotype":{"types":[{"id":"HP:0006808","label":"Cerebral hypomyelination"}]}},{"entity":"FlyBase:FBal0205457","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"FlyBase:FBal0208360","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:143818","phenotype":{"types":[{"id":"HP:0002376","label":"Developmental regression"}]}},{"entity":"ClinVarVariant:39715","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:210399","phenotype":{"types":[{"id":"HP:0011362","label":"Abnormal hair quantity"}]}},{"entity":"ClinVarVariant:94837","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"MGI:5468252","phenotype":{"types":[{"id":"MP:0011167","label":"abnormal adipose tissue development"}]}},{"entity":"FlyBase:FBal0203318","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:42391","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"ClinVarVariant:333","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"MGI:4360523","phenotype":{"types":[{"id":"MP:0003697","label":"absent zona pellucida"}]}},{"entity":"ClinVarVariant:127329","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:12586","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:217078","phenotype":{"types":[{"id":"HP:0007440","label":"Generalized hyperpigmentation"}]}},{"entity":"ClinVarVariant:54084","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:211656","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"MGI:4939621","phenotype":{"types":[{"id":"MP:0005670","label":"abnormal white adipose tissue physiology"}]}},{"entity":"FlyBase:FBal0260939","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:2267","phenotype":{"types":[{"id":"HP:0100279","label":"Ulcerative colitis"}]}},{"entity":"ClinVarVariant:137984","phenotype":{"types":[{"id":"HP:0000707","label":"Abnormality of the nervous system"}]}},{"entity":"MGI:3810074","phenotype":{"types":[{"id":"MP:0005092","label":"decreased double-positive T cell number"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002299-WBRNAi00078911","phenotype":{"types":[{"id":"WBPhenotype:0000666","label":"ovulation variant"}]}},{"entity":"ClinVarVariant:210464","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:215893","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:41085","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:133628","phenotype":{"types":[{"id":"HP:0002344","label":"Progressive neurologic deterioration"}]}},{"entity":"ClinVarVariant:180354","phenotype":{"types":[{"id":"HP:0002631","label":"Ascending aortic aneurysm"}]}},{"entity":"ClinVarVariant:135745","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:208846","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"MGI:2158692","phenotype":{"types":[{"id":"MP:0002566","label":"abnormal sexual interaction"}]}},{"entity":"MGI:2183240","phenotype":{"types":[{"id":"MP:0006143","label":"increased systemic arterial diastolic blood pressure"}]}},{"entity":"ClinVarVariant:41001","phenotype":{"types":[{"id":"HP:0001376","label":"Limitation of joint mobility"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00021604-WBRNAi00007532","phenotype":{"types":[{"id":"WBPhenotype:0001119","label":"cell cycle slow early emb"}]}},{"entity":"ClinVarVariant:128203","phenotype":{"types":[{"id":"HP:0000520","label":"Proptosis"}]}},{"entity":"ClinVarVariant:9966","phenotype":{"types":[{"id":"HP:0001923","label":"Reticulocytosis"}]}},{"entity":"ClinVarVariant:31190","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"ClinVarVariant:216404","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:120223","phenotype":{"types":[{"id":"HP:0000953","label":"Hyperpigmentation of the skin"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000912-WBRNAi00066508","phenotype":{"types":[{"id":"WBPhenotype:0000061","label":"extended life span"}]}},{"entity":"ClinVarVariant:10259","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:3773724","phenotype":{"types":[{"id":"MP:0001265","label":"decreased body size"}]}},{"entity":"ClinVarVariant:216414","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:53459","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017967-WBRNAi00000357","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:343","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"MGI:2153811","phenotype":{"types":[{"id":"MP:0000035","label":"abnormal membranous labyrinth morphology"}]}},{"entity":"ClinVarVariant:97534","phenotype":{"types":[{"id":"HP:0000999","label":"Pyoderma"}]}},{"entity":"ClinVarVariant:30262","phenotype":{"types":[{"id":"HP:0000546","label":"Retinal degeneration"}]}},{"entity":"ClinVarVariant:56237","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:4784","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:188125","phenotype":{"types":[{"id":"HP:0012539","label":"Non-Hodgkin lymphoma"}]}},{"entity":"ClinVarVariant:50237","phenotype":{"types":[{"id":"HP:0003300","label":"Ovoid vertebral bodies"}]}},{"entity":"ClinVarVariant:100931","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:9993","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:132699","phenotype":{"types":[{"id":"HP:0001161","label":"Hand polydactyly"}]}},{"entity":"FlyBase:FBal0277862","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ZFIN:ZDB-ALT-121128-4","phenotype":{"types":[{"id":"ZP:0002448","label":"abnormal(ly) disorganized retinal outer nuclear layer"}]}},{"entity":"ClinVarVariant:158984","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:5855","phenotype":{"types":[{"id":"HP:0000217","label":"Xerostomia"}]}},{"entity":"ClinVarVariant:14030","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:210007","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"FlyBase:FBal0098633","phenotype":{"types":[{"id":"FBcv:0000364","label":"sterile"}]}},{"entity":"ClinVarVariant:216764","phenotype":{"types":[{"id":"HP:0000256","label":"Macrocephaly"}]}},{"entity":"ClinVarVariant:143828","phenotype":{"types":[{"id":"HP:0002376","label":"Developmental regression"}]}},{"entity":"ClinVarVariant:96607","phenotype":{"types":[{"id":"HP:0010906","label":"Hyperhistidinemia"}]}},{"entity":"MGI:2651830","phenotype":{"types":[{"id":"MP:0001053","label":"abnormal neuromuscular synapse morphology"}]}},{"entity":"ClinVarVariant:88650","phenotype":{"types":[{"id":"HP:0002408","label":"Cerebral arteriovenous malformation"}]}},{"entity":"FlyBase:FBal0304837","phenotype":{"types":[{"id":"FBbt:00001778PHENOTYPE","label":"Drosophila wing disc phenotype"}]}},{"entity":"ClinVarVariant:162493","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:35601","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:1282","phenotype":{"types":[{"id":"HP:0003398","label":"Abnormal synaptic transmission at the neuromuscular junction"}]}},{"entity":"ClinVarVariant:36041","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:21545","phenotype":{"types":[{"id":"HP:0001256","label":"Intellectual disability, mild"}]}},{"entity":"ClinVarVariant:65068","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:13909","phenotype":{"types":[{"id":"HP:0002527","label":"Falls"}]}},{"entity":"ClinVarVariant:162416","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"dbSNP:rs110710505","phenotype":{"types":[{"id":"AQTLTrait:1120","label":"Thurl width"}]}},{"entity":"ClinVarVariant:5867","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:216132","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:142766","phenotype":{"types":[{"id":"HP:0001067","label":"Neurofibromas"}]}},{"entity":"ClinVarVariant:592","phenotype":{"types":[{"id":"HP:0002286","label":"Fair hair"}]}},{"entity":"ClinVarVariant:94437","phenotype":{"types":[{"id":"HP:0001371","label":"Flexion contracture"}]}},{"entity":"ClinVarVariant:13326","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"ClinVarVariant:7726","phenotype":{"types":[{"id":"HP:0000114","label":"Proximal tubulopathy"}]}},{"entity":"MGI:3624262","phenotype":{"types":[{"id":"HP:0000089","label":"Renal hypoplasia"}]}},{"entity":"ClinVarVariant:49932","phenotype":{"types":[{"id":"HP:0006772","label":"Renal angiomyolipoma"}]}},{"entity":"MGI:4262238","phenotype":{"types":[{"id":"GO:0003351PHENOTYPE","label":"epithelial cilium movement phenotype"}]}},{"entity":"ClinVarVariant:65879","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"FlyBase:FBal0297156","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:101115","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"ClinVarVariant:53185","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"ClinVarVariant:209063","phenotype":{"types":[{"id":"HP:0001648","label":"Cor pulmonale"}]}},{"entity":"ClinVarVariant:56283","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:10629","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:127244","phenotype":{"types":[{"id":"HP:0008734","label":"Decreased testicular size"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001102-WBRNAi00067595","phenotype":{"types":[{"id":"WBPhenotype:0000531","label":"organism development variant"}]}},{"entity":"ClinVarVariant:67858","phenotype":{"types":[{"id":"HP:0004756","label":"Ventricular tachycardia"}]}},{"entity":"ClinVarVariant:135922","phenotype":{"types":[{"id":"HP:0002672","label":"Gastrointestinal carcinoma"}]}},{"entity":"ClinVarVariant:35825","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:39594","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:143592","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"MGI:2152978","phenotype":{"types":[{"id":"MP:0004669","label":"enlarged vertebral body"}]}},{"entity":"FlyBase:FBal0210008","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:179260","phenotype":{"types":[{"id":"HP:0000358","label":"Posteriorly rotated ears"}]}},{"entity":"ClinVarVariant:53376","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:40680","phenotype":{"types":[{"id":"HP:0003010","label":"Prolonged bleeding time"}]}},{"entity":"ClinVarVariant:21242","phenotype":{"types":[{"id":"HP:0000202","label":"Oral cleft"}]}},{"entity":"ClinVarVariant:211666","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:3441","phenotype":{"types":[{"id":"HP:0001199","label":"Triphalangeal thumb"}]}},{"entity":"ClinVarVariant:17082","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:159244","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"MGI:2148205","phenotype":{"types":[{"id":"MP:0004236","label":"absent masseter muscle"}]}},{"entity":"ClinVarVariant:9246","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:188766","phenotype":{"types":[{"id":"HP:0000635","label":"Blue irides"}]}},{"entity":"ClinVarVariant:24502","phenotype":{"types":[{"id":"HP:0000099","label":"Glomerulonephritis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00012632-WBRNAi00067998","phenotype":{"types":[{"id":"WBPhenotype:0000531","label":"organism development variant"}]}},{"entity":"ClinVarVariant:24601","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:188938","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"ClinVarVariant:10263","phenotype":{"types":[{"id":"HP:0005681","label":"Juvenile rheumatoid arthritis"}]}},{"entity":"ClinVarVariant:49641","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"MGI:3771975","phenotype":{"types":[{"id":"MP:0000458","label":"abnormal mandible morphology"}]}},{"entity":"MGI:3765956","phenotype":{"types":[{"id":"GO:0042981PHENOTYPE","label":"regulation of apoptotic process phenotype"}]}},{"entity":"ClinVarVariant:18452","phenotype":{"types":[{"id":"HP:0000047","label":"Hypospadias"}]}},{"entity":"ClinVarVariant:29740","phenotype":{"types":[{"id":"HP:0010628","label":"Facial palsy"}]}},{"entity":"ClinVarVariant:216584","phenotype":{"types":[{"id":"HP:0006771","label":"Duodenal adenocarcinoma"}]}},{"entity":"ClinVarVariant:204313","phenotype":{"types":[{"id":"HP:0001989","label":"Fetal akinesia sequence"}]}},{"entity":"ClinVarVariant:4442","phenotype":{"types":[{"id":"HP:0001947","label":"Renal tubular acidosis"}]}},{"entity":"ClinVarVariant:120219","phenotype":{"types":[{"id":"HP:0001055","label":"Erysipelas"}]}},{"entity":"ClinVarVariant:158070","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:93153","phenotype":{"types":[{"id":"HP:0002202","label":"Pleural effusion"}]}},{"entity":"ClinVarVariant:12391","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:97700","phenotype":{"types":[{"id":"HP:0001596","label":"Alopecia"}]}},{"entity":"ClinVarVariant:10832","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"MGI:3778272","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:16646","phenotype":{"types":[{"id":"HP:0007110","label":"Central hypoventilation"}]}},{"entity":"ClinVarVariant:49661","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:24686","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"ClinVarVariant:158186","phenotype":{"types":[{"id":"HP:0011097","label":"Epileptic spasms"}]}},{"entity":"FlyBase:FBal0300880","phenotype":{"types":[{"id":"GO:0005634PHENOTYPE","label":"nucleus phenotype"}]}},{"entity":"ClinVarVariant:25360","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"WormBase:WBVar00144564","phenotype":{"types":[{"id":"WBPhenotype:0000687","label":"feminization of XX and XO animals"}]}},{"entity":"FlyBase:FBal0213074","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:52378","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"MGI:5518726","phenotype":{"types":[{"id":"MP:0000715","label":"decreased thymocyte number"}]}},{"entity":"ClinVarVariant:135736","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"_:genid1974728","phenotype":{"types":[{"id":"ZP:0001828","label":"abnormal(ly) malformed post-vent region"}]}},{"entity":"ClinVarVariant:5095","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"MGI:2183400","phenotype":{"types":[{"id":"MP:0005026","label":"decreased susceptibility to parasitic infection"}]}},{"entity":"ClinVarVariant:16275","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:2180768","phenotype":{"types":[{"id":"HP:0000777","label":"Abnormality of the thymus"}]}},{"entity":"MGI:5449635","phenotype":{"types":[{"id":"MP:0001661","label":"extended life span"}]}},{"entity":"FlyBase:FBal0268099","phenotype":{"types":[{"id":"FBbt:00004508PHENOTYPE","label":"eye phenotype"}]}},{"entity":"ClinVarVariant:3766","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:55941","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:53915","phenotype":{"types":[{"id":"HP:0010943","label":"Echogenic fetal bowel"}]}},{"entity":"ClinVarVariant:126447","phenotype":{"types":[{"id":"HP:0000613","label":"Photophobia"}]}},{"entity":"ClinVarVariant:353","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:211728","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"ClinVarVariant:24518","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:216185","phenotype":{"types":[{"id":"HP:0006744","label":"Adrenocortical carcinoma"}]}},{"entity":"MGI:2384163","phenotype":{"types":[{"id":"MP:0000351","label":"increased cell proliferation"}]}},{"entity":"ClinVarVariant:56687","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"ClinVarVariant:1137","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:36494","phenotype":{"types":[{"id":"HP:0004879","label":"Intermittent hyperventilation"}]}},{"entity":"ClinVarVariant:158994","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:14870","phenotype":{"types":[{"id":"HP:0010049","label":"Short metacarpal"}]}},{"entity":"ClinVarVariant:54013","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:208563","phenotype":{"types":[{"id":"HP:0001397","label":"Hepatic steatosis"}]}},{"entity":"FlyBase:FBal0209552","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:211312","phenotype":{"types":[{"id":"HP:0000445","label":"Wide nose"}]}},{"entity":"ClinVarVariant:13624","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:25335","phenotype":{"types":[{"id":"HP:0012023","label":"Galactosuria"}]}},{"entity":"ClinVarVariant:21575","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:216875","phenotype":{"types":[{"id":"HP:0002247","label":"Duodenal atresia"}]}},{"entity":"ClinVarVariant:41122","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:54094","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:53628","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:53903","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:188883","phenotype":{"types":[{"id":"HP:0001947","label":"Renal tubular acidosis"}]}},{"entity":"ClinVarVariant:101165","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:50106","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"MGI:5588201","phenotype":{"types":[{"id":"MP:0001685","label":"abnormal endoderm development"}]}},{"entity":"ClinVarVariant:30204","phenotype":{"types":[{"id":"HP:0000577","label":"Exotropia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011067-WBRNAi00081161","phenotype":{"types":[{"id":"WBPhenotype:0001569","label":"body wall muscle myosin organization defective"}]}},{"entity":"MGI:2679886","phenotype":{"types":[{"id":"HP:0012535","label":"Abnormal synaptic transmission"}]}},{"entity":"dbSNP:rs7787531","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"ClinVarVariant:179299","phenotype":{"types":[{"id":"HP:0004309","label":"Ventricular preexcitation"}]}},{"entity":"ClinVarVariant:50854","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:53945","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:25205","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:9120","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"ClinVarVariant:135872","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:56595","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"ClinVarVariant:56615","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"FlyBase:FBal0239685","phenotype":{"types":[{"id":"FBbt:00004729PHENOTYPE","label":"Drosophila wing phenotype"}]}},{"entity":"ClinVarVariant:9551","phenotype":{"types":[{"id":"HP:0002401","label":"Stroke-like episodes"}]}},{"entity":"ClinVarVariant:49651","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:110","phenotype":{"types":[{"id":"HP:0002321","label":"Vertigo"}]}},{"entity":"MGI:3054960","phenotype":{"types":[{"id":"MP:0001928","label":"abnormal ovulation"}]}},{"entity":"ClinVarVariant:82640","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:2216","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"ClinVarVariant:4034","phenotype":{"types":[{"id":"HP:0000158","label":"Macroglossia"}]}},{"entity":"ClinVarVariant:8963","phenotype":{"types":[{"id":"HP:0000126","label":"Hydronephrosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002251-WBRNAi00063113","phenotype":{"types":[{"id":"WBPhenotype:0000523","label":"chemical response variant"}]}},{"entity":"AQTL:25943","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:53544","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"FlyBase:FBal0258455","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:189716","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:135929","phenotype":{"types":[{"id":"HP:0100615","label":"Ovarian neoplasm"}]}},{"entity":"ClinVarVariant:39","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:215576","phenotype":{"types":[{"id":"HP:0005550","label":"Chronic lymphatic leukemia"}]}},{"entity":"MGI:1856699","phenotype":{"types":[{"id":"MP:0000376","label":"folliculitis"}]}},{"entity":"ClinVarVariant:127144","phenotype":{"types":[{"id":"HP:0002078","label":"Truncal ataxia"}]}},{"entity":"MGI:1857734","phenotype":{"types":[{"id":"MP:0011084","label":"lethality at weaning, incomplete penetrance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00018892-WBRNAi00000065","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:43612","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:163462","phenotype":{"types":[{"id":"HP:0002097","label":"Emphysema"}]}},{"entity":"FlyBase:FBal0128189","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:4387","phenotype":{"types":[{"id":"HP:0002486","label":"Myotonia"}]}},{"entity":"ClinVarVariant:95023","phenotype":{"types":[{"id":"HP:0007018","label":"Attention deficit hyperactivity disorder"}]}},{"entity":"ClinVarVariant:136194","phenotype":{"types":[{"id":"HP:0000157","label":"Abnormality of the tongue"}]}},{"entity":"ClinVarVariant:25320","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:38921","phenotype":{"types":[{"id":"HP:0001888","label":"Lymphopenia"}]}},{"entity":"ClinVarVariant:101118","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"dbSNP:rs41643216","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:211716","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"MGI:1857212","phenotype":{"types":[{"id":"GO:0030301PHENOTYPE","label":"cholesterol transport phenotype"}]}},{"entity":"ClinVarVariant:40562","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:97035","phenotype":{"types":[{"id":"HP:0000023","label":"Inguinal hernia"}]}},{"entity":"ClinVarVariant:24289","phenotype":{"types":[{"id":"HP:0000613","label":"Photophobia"}]}},{"entity":"AQTL:41940","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:68302","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"dbSNP:rs5219","phenotype":{"types":[{"id":"HP:0001254","label":"Lethargy"}]}},{"entity":"ClinVarVariant:83166","phenotype":{"types":[{"id":"HP:0006740","label":"Transitional cell carcinoma of the bladder"}]}},{"entity":"FlyBase:FBal0205897","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:21164","phenotype":{"types":[{"id":"HP:0002827","label":"Hip dislocation"}]}},{"entity":"FlyBase:FBal0102923","phenotype":{"types":[{"id":"FBbt:00005177PHENOTYPE","label":"Drosophila chaeta phenotype"}]}},{"entity":"MGI:1933748","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:135879","phenotype":{"types":[{"id":"HP:0010767","label":"Sacrococcygeal pilonidal abnormality"}]}},{"entity":"ClinVarVariant:56293","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:35835","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:39071","phenotype":{"types":[{"id":"HP:0009769","label":"Bullet-shaped phalanges of the hand"}]}},{"entity":"MGI:2668394","phenotype":{"types":[{"id":"HP:0002414","label":"Spina bifida"}]}},{"entity":"ClinVarVariant:38377","phenotype":{"types":[{"id":"HP:0002172","label":"Postural instability"}]}},{"entity":"ClinVarVariant:11846","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:53690","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00021829-WBRNAi00004730","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:53794","phenotype":{"types":[{"id":"HP:0100598","label":"Pulmonary edema"}]}},{"entity":"MGI:4948909","phenotype":{"types":[{"id":"MP:0004952","label":"increased spleen weight"}]}},{"entity":"ClinVarVariant:204087","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"MGI:2178475","phenotype":{"types":[{"id":"HP:0011014","label":"Abnormal glucose homeostasis"}]}},{"entity":"ClinVarVariant:132749","phenotype":{"types":[{"id":"HP:0011069","label":"Increased number of teeth"}]}},{"entity":"ClinVarVariant:49681","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"MGI:3530077","phenotype":{"types":[{"id":"MP:0001513","label":"limb grasping"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022017-WBRNAi00090877","phenotype":{"types":[{"id":"WBPhenotype:0002095","label":"lysosome-related organelle morphology variant"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-030131-1213-ZDB-MRPHLNO-131120-6","phenotype":{"types":[{"id":"ZP:0004518","label":"abnormal(ly) immature eye"}]}},{"entity":"ClinVarVariant:14214","phenotype":{"types":[{"id":"HP:0001732","label":"Abnormality of the pancreas"}]}},{"entity":"MGI:2180880","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"ClinVarVariant:216023","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:1855960","phenotype":{"types":[{"id":"MP:0005075","label":"abnormal melanosome morphology"}]}},{"entity":"ClinVarVariant:53370","phenotype":{"types":[{"id":"HP:0000027","label":"Azoospermia"}]}},{"entity":"ClinVarVariant:31851","phenotype":{"types":[{"id":"HP:0000944","label":"Abnormality of the metaphyses"}]}},{"entity":"MGI:1856209","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:3187","phenotype":{"types":[{"id":"HP:0010049","label":"Short metacarpal"}]}},{"entity":"ClinVarVariant:50040","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"ClinVarVariant:190786","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:161239","phenotype":{"types":[{"id":"HP:0007293","label":"Anterior sacral meningocele"}]}},{"entity":"ClinVarVariant:29943","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ZFIN:ZDB-ALT-030919-2","phenotype":{"types":[{"id":"ZP:0009068","label":"abnormal(ly) disrupted spinal cord oligodendrocyte cell differentiation"}]}},{"entity":"FlyBase:FBal0239048","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:14718","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:40186","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:156282","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"MGI:3845227","phenotype":{"types":[{"id":"HP:0005563","label":"Decreased numbers of nephrons"}]}},{"entity":"ClinVarVariant:53858","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"FlyBase:FBal0207413","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:4443","phenotype":{"types":[{"id":"HP:0008682","label":"Acute tubular necrosis"}]}},{"entity":"ClinVarVariant:13503","phenotype":{"types":[{"id":"HP:0002171","label":"Gliosis"}]}},{"entity":"ClinVarVariant:8189","phenotype":{"types":[{"id":"HP:0002196","label":"Myelopathy"}]}},{"entity":"ClinVarVariant:38980","phenotype":{"types":[{"id":"HP:0003458","label":"EMG: myopathic abnormalities"}]}},{"entity":"ClinVarVariant:136167","phenotype":{"types":[{"id":"HP:0001578","label":"Hypercortisolism"}]}},{"entity":"ClinVarVariant:13960","phenotype":{"types":[{"id":"HP:0001640","label":"Cardiomegaly"}]}},{"entity":"ClinVarVariant:21166","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:1333","phenotype":{"types":[{"id":"HP:0000601","label":"Hypotelorism"}]}},{"entity":"MGI:4429385","phenotype":{"types":[{"id":"MP:0001364","label":"decreased anxiety-related response"}]}},{"entity":"ClinVarVariant:53992","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:41462","phenotype":{"types":[{"id":"HP:0000473","label":"Torticollis"}]}},{"entity":"MGI:3716074","phenotype":{"types":[{"id":"MP:0005332","label":"abnormal amino acid level"}]}},{"entity":"ClinVarVariant:180305","phenotype":{"types":[{"id":"HP:0001519","label":"Disproportionate tall stature"}]}},{"entity":"ClinVarVariant:48806","phenotype":{"types":[{"id":"HP:0009720","label":"Adenoma sebaceum"}]}},{"entity":"FlyBase:FBal0183239","phenotype":{"types":[{"id":"FBbt:00005156PHENOTYPE","label":"Drosophila mechanosensory sensory organ phenotype"}]}},{"entity":"ClinVarVariant:49247","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"ClinVarVariant:35753","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"MGI:1931048","phenotype":{"types":[{"id":"MP:0005325","label":"abnormal renal glomerulus morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006917-WBRNAi00040864","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"ClinVarVariant:21779","phenotype":{"types":[{"id":"HP:0002411","label":"Myokymia"}]}},{"entity":"ClinVarVariant:127349","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:21218","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"WormBase:WBVar00143078","phenotype":{"types":[{"id":"WBPhenotype:0001652","label":"anchor cell invasion variant"}]}},{"entity":"ClinVarVariant:49810","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:53356","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:17272","phenotype":{"types":[{"id":"HP:0002273","label":"Tetraparesis"}]}},{"entity":"ClinVarVariant:211467","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:10204","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:6542","phenotype":{"types":[{"id":"HP:0001805","label":"Thick nail"}]}},{"entity":"ClinVarVariant:10822","phenotype":{"types":[{"id":"HP:0002757","label":"Recurrent fractures"}]}},{"entity":"ClinVarVariant:5449","phenotype":{"types":[{"id":"HP:0002671","label":"Basal cell carcinoma"}]}},{"entity":"ClinVarVariant:180392","phenotype":{"types":[{"id":"HP:0011034","label":"Amyloidosis"}]}},{"entity":"ClinVarVariant:5905","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:41187","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004506-WBRNAi00078787","phenotype":{"types":[{"id":"WBPhenotype:0001171","label":"shortened life span"}]}},{"entity":"ClinVarVariant:21451","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:2628","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:50060","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"ClinVarVariant:12965","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:2453","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:210427","phenotype":{"types":[{"id":"HP:0005599","label":"Hypopigmentation of hair"}]}},{"entity":"ClinVarVariant:53863","phenotype":{"types":[{"id":"HP:0010943","label":"Echogenic fetal bowel"}]}},{"entity":"ClinVarVariant:215894","phenotype":{"types":[{"id":"HP:0000012","label":"Urinary urgency"}]}},{"entity":"ClinVarVariant:9714","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"MGI:3836429","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:8061","phenotype":{"types":[{"id":"HP:0006443","label":"Patellar aplasia"}]}},{"entity":"ClinVarVariant:217068","phenotype":{"types":[{"id":"HP:0007440","label":"Generalized hyperpigmentation"}]}},{"entity":"ClinVarVariant:54053","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:209164","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"FlyBase:FBal0195554","phenotype":{"types":[{"id":"FBbt:00001311PHENOTYPE","label":"interface glial cell phenotype"}]}},{"entity":"FlyBase:FBal0209714","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"FlyBase:FBal0091132","phenotype":{"types":[{"id":"FBbt:00004642PHENOTYPE","label":"Drosophila tibia phenotype"}]}},{"entity":"ClinVarVariant:189261","phenotype":{"types":[{"id":"HP:0001284","label":"Areflexia"}]}},{"entity":"ClinVarVariant:10915","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:39848","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"dbSNP:rs110754910","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:93724","phenotype":{"types":[{"id":"HP:0006979","label":"Sleep-wake cycle disturbance"}]}},{"entity":"ClinVarVariant:25231","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"MGI:3656024","phenotype":{"types":[{"id":"MP:0000228","label":"abnormal thrombopoiesis"}]}},{"entity":"ClinVarVariant:5312","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004188-WBRNAi00095757","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:68288","phenotype":{"types":[{"id":"HP:0001874","label":"Abnormality of neutrophils"}]}},{"entity":"ClinVarVariant:53660","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"ClinVarVariant:8184","phenotype":{"types":[{"id":"HP:0003095","label":"Septic arthritis"}]}},{"entity":"ClinVarVariant:30988","phenotype":{"types":[{"id":"HP:0001845","label":"Overlapping toe"}]}},{"entity":"ZFIN:ZDB-ALT-050916-14","phenotype":{"types":[{"id":"ZP:0004993","label":"abnormal(ly) constricted heart"}]}},{"entity":"ClinVarVariant:53943","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"MGI:5466366","phenotype":{"types":[{"id":"MP:0001513","label":"limb grasping"}]}},{"entity":"ClinVarVariant:53935","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:56613","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:183678","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:16879","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:38752","phenotype":{"types":[{"id":"HP:0000519","label":"Congenital cataract"}]}},{"entity":"ClinVarVariant:182386","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:65739","phenotype":{"types":[{"id":"HP:0000691","label":"Microdontia"}]}},{"entity":"ClinVarVariant:53841","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:66439","phenotype":{"types":[{"id":"HP:0011441","label":"Abnormality of the medulla oblongata"}]}},{"entity":"ClinVarVariant:2259","phenotype":{"types":[{"id":"HP:0001287","label":"Meningitis"}]}},{"entity":"ClinVarVariant:1703","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"_:genid1976040","phenotype":{"types":[{"id":"ZP:0002310","label":"abnormal(ly) circling whole organism"}]}},{"entity":"dbSNP:rs12386026","phenotype":{"types":[{"id":"HP:0006516","label":"Hypersensitivity pneumonitis"}]}},{"entity":"MGI:3761621","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:211746","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:158392","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ClinVarVariant:12641","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"MGI:4432238","phenotype":{"types":[{"id":"MP:0004889","label":"increased energy expenditure"}]}},{"entity":"ClinVarVariant:217052","phenotype":{"types":[{"id":"HP:0100697","label":"Neurofibrosarcoma"}]}},{"entity":"ClinVarVariant:11129","phenotype":{"types":[{"id":"HP:0005549","label":"Congenital neutropenia"}]}},{"entity":"ClinVarVariant:56034","phenotype":{"types":[{"id":"HP:0000815","label":"Hypergonadotropic hypogonadism"}]}},{"entity":"ClinVarVariant:6286","phenotype":{"types":[{"id":"HP:0000925","label":"Abnormality of the vertebral column"}]}},{"entity":"ClinVarVariant:9960","phenotype":{"types":[{"id":"HP:0004936","label":"Venous thrombosis"}]}},{"entity":"ClinVarVariant:64779","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"ClinVarVariant:56635","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"MGI:2158457","phenotype":{"types":[{"id":"MP:0000527","label":"abnormal kidney development"}]}},{"entity":"ClinVarVariant:100671","phenotype":{"types":[{"id":"HP:0004719","label":"Hyperechogenic kidneys"}]}},{"entity":"ClinVarVariant:12791","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:101135","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"ClinVarVariant:189852","phenotype":{"types":[{"id":"HP:0002384","label":"Focal seizures with impairment of consciousness or awareness"}]}},{"entity":"AQTL:20678","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:13340","phenotype":{"types":[{"id":"HP:0004808","label":"Acute myeloid leukemia"}]}},{"entity":"ClinVarVariant:40490","phenotype":{"types":[{"id":"HP:0100495","label":"Mastocytosis"}]}},{"entity":"ClinVarVariant:94601","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"WormBase:WBVar00531947","phenotype":{"types":[{"id":"WBPhenotype:0000138","label":"lipid composition variant"}]}},{"entity":"MGI:3712283","phenotype":{"types":[{"id":"MP:0006316","label":"increased urine sodium level"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017983-WBRNAi00075550","phenotype":{"types":[{"id":"WBPhenotype:0000032","label":"sick"}]}},{"entity":"ClinVarVariant:44631","phenotype":{"types":[{"id":"HP:0000179","label":"Thick lower lip vermilion"}]}},{"entity":"MGI:5317762","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"MGI:2153094","phenotype":{"types":[{"id":"HP:0001397","label":"Hepatic steatosis"}]}},{"entity":"MGI:5467564","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:132733","phenotype":{"types":[{"id":"HP:0100777","label":"Exostoses"}]}},{"entity":"ClinVarVariant:53794","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:1568","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:5502","phenotype":{"types":[{"id":"HP:0200094","label":"Frontal open bite"}]}},{"entity":"MGI:3043520","phenotype":{"types":[{"id":"MP:0004952","label":"increased spleen weight"}]}},{"entity":"MGI:2157350","phenotype":{"types":[{"id":"GO:0030900PHENOTYPE","label":"forebrain development phenotype"}]}},{"entity":"ClinVarVariant:17189","phenotype":{"types":[{"id":"HP:0000768","label":"Pectus carinatum"}]}},{"entity":"ClinVarVariant:18025","phenotype":{"types":[{"id":"HP:0004850","label":"Recurrent deep vein thrombosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006975-WBRNAi00081919","phenotype":{"types":[{"id":"WBPhenotype:0001595","label":"somatic transgene silencing variant"}]}},{"entity":"ClinVarVariant:100719","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:9454","phenotype":{"types":[{"id":"HP:0000529","label":"Progressive visual loss"}]}},{"entity":"ClinVarVariant:53366","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004453-WBRNAi00072949","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:204127","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:1236","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"ClinVarVariant:48912","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"ClinVarVariant:8212","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:30180","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007030-WBRNAi00026587","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}}],"schema":"phenopacket-level-1"},"params":{"q":"*:*","fq":"(subject_closure:\"HP:0002548\")","personality":"variant_phenotype","showEmptyFields":false},"name":"Monarch Application","date":"Sun Jun 26 2016 12:07:13 GMT-0700 (PDT)"}
\ No newline at end of file
diff -r 000000000000 -r 850bb90bd667 test-data/phenotypes-for-variants-intersection.json
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/phenotypes-for-variants-intersection.json Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,1 @@
+{"phenopacket":{"phenotype_profile":[{"entity":"ClinVarVariant:217207","phenotype":{"types":[{"id":"HP:0010535","label":"Sleep apnea"}]}},{"entity":"FlyBase:FBal0213223","phenotype":{"types":[{"id":"FBcv:0000352","label":"partially lethal - majority die"}]}},{"entity":"ClinVarVariant:11487","phenotype":{"types":[{"id":"HP:0001829","label":"Foot polydactyly"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022219-WBRNAi00094335","phenotype":{"types":[{"id":"WBPhenotype:0000508","label":"nonsense mRNA accumulation"}]}},{"entity":"FlyBase:FBal0204990","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"FlyBase:FBal0094697","phenotype":{"types":[{"id":"FBcv:0000395","label":"locomotor rhythm defective"}]}},{"entity":"ClinVarVariant:126392","phenotype":{"types":[{"id":"HP:0001433","label":"Hepatosplenomegaly"}]}},{"entity":"ClinVarVariant:167486","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:161253","phenotype":{"types":[{"id":"HP:0011096","label":"Peripheral demyelination"}]}},{"entity":"ClinVarVariant:24488","phenotype":{"types":[{"id":"HP:0000517","label":"Abnormality of the lens"}]}},{"entity":"ClinVarVariant:10038","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"ClinVarVariant:120292","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:91630","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:188714","phenotype":{"types":[{"id":"HP:0002015","label":"Dysphagia"}]}},{"entity":"ClinVarVariant:65078","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:13919","phenotype":{"types":[{"id":"HP:0002527","label":"Falls"}]}},{"entity":"ClinVarVariant:166796","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"ClinVarVariant:53300","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:49671","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:6383","phenotype":{"types":[{"id":"HP:0002758","label":"Osteoarthritis"}]}},{"entity":"ClinVarVariant:12869","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:3241","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"MGI:1856875","phenotype":{"types":[{"id":"MP:0000377","label":"abnormal hair follicle morphology"}]}},{"entity":"ClinVarVariant:24448","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"NCBIGene:553991","phenotype":{"types":[{"id":"HP:0003805","label":"Rimmed vacuoles"}]}},{"entity":"ClinVarVariant:35614","phenotype":{"types":[{"id":"HP:0001518","label":"Small for gestational age"}]}},{"entity":"ClinVarVariant:24856","phenotype":{"types":[{"id":"HP:0001636","label":"Tetralogy of Fallot"}]}},{"entity":"ClinVarVariant:135244","phenotype":{"types":[{"id":"HP:0100819","label":"Intestinal fistula"}]}},{"entity":"MGI:3702572","phenotype":{"types":[{"id":"MP:0001327","label":"decreased retinal photoreceptor cell number"}]}},{"entity":"ClinVarVariant:204248","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002981-WBRNAi00083915","phenotype":{"types":[{"id":"WBPhenotype:0001171","label":"shortened life span"}]}},{"entity":"ClinVarVariant:10490","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007201-WBRNAi00062819","phenotype":{"types":[{"id":"WBPhenotype:0000691","label":"gonad development variant"}]}},{"entity":"MGI:2182460","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"dbSNP:rs2202157","phenotype":{"types":[{"id":"HP:0009733","label":"Glioma"}]}},{"entity":"ClinVarVariant:49410","phenotype":{"types":[{"id":"HP:0100764","label":"Lymphangioma"}]}},{"entity":"ClinVarVariant:101209","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"MGI:2684419","phenotype":{"types":[{"id":"MP:0008190","label":"decreased transitional stage B cell number"}]}},{"entity":"MGI:2671609","phenotype":{"types":[{"id":"MP:0011279","label":"decreased ear pigmentation"}]}},{"entity":"ClinVarVariant:215956","phenotype":{"types":[{"id":"HP:0000324","label":"Facial asymmetry"}]}},{"entity":"ClinVarVariant:49985","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"dbSNP:rs1819084","phenotype":{"types":[{"id":"HP:0002721","label":"Immunodeficiency"}]}},{"entity":"ClinVarVariant:42347","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"ClinVarVariant:10746","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"dbSNP:rs10720414","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"ClinVarVariant:100901","phenotype":{"types":[{"id":"HP:0008420","label":"Punctate vertebral calcifications"}]}},{"entity":"ClinVarVariant:40523","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:3975","phenotype":{"types":[{"id":"HP:0000121","label":"Nephrocalcinosis"}]}},{"entity":"ClinVarVariant:191776","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:3243","phenotype":{"types":[{"id":"HP:0001274","label":"Agenesis of corpus callosum"}]}},{"entity":"ClinVarVariant:49691","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:53303","phenotype":{"types":[{"id":"HP:0100732","label":"Pancreatic fibrosis"}]}},{"entity":"MGI:3046930","phenotype":{"types":[{"id":"MP:0008828","label":"abnormal lymph node cell ratio"}]}},{"entity":"ClinVarVariant:10947","phenotype":{"types":[{"id":"HP:0002007","label":"Frontal bossing"}]}},{"entity":"ClinVarVariant:208036","phenotype":{"types":[{"id":"HP:0000280","label":"Coarse facial features"}]}},{"entity":"ClinVarVariant:216123","phenotype":{"types":[{"id":"HP:0001350","label":"Slurred speech"}]}},{"entity":"ClinVarVariant:10634","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"ClinVarVariant:13684","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:53955","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:42536","phenotype":{"types":[{"id":"HP:0001297","label":"Stroke"}]}},{"entity":"dbSNP:rs109157116","phenotype":{"types":[{"id":"AQTLTrait:1067","label":"Length of productive life"}]}},{"entity":"ClinVarVariant:143822","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:208497","phenotype":{"types":[{"id":"HP:0002179","label":"Opisthotonus"}]}},{"entity":"ClinVarVariant:42838","phenotype":{"types":[{"id":"HP:0003712","label":"Skeletal muscle hypertrophy"}]}},{"entity":"ClinVarVariant:53165","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"MGI:2159365","phenotype":{"types":[{"id":"HP:0005528","label":"Bone marrow hypocellularity"}]}},{"entity":"ClinVarVariant:65088","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:40601","phenotype":{"types":[{"id":"HP:0008443","label":"Spinal deformities"}]}},{"entity":"ClinVarVariant:10128","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"MGI:2178049","phenotype":{"types":[{"id":"MP:0001405","label":"impaired coordination"}]}},{"entity":"FlyBase:FBal0294203","phenotype":{"types":[{"id":"FBbt:00001920PHENOTYPE","label":"embryonic/larval brain phenotype"}]}},{"entity":"ClinVarVariant:5007","phenotype":{"types":[{"id":"HP:0001182","label":"Tapered finger"}]}},{"entity":"ClinVarVariant:363","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:184551","phenotype":{"types":[{"id":"HP:0002216","label":"Premature graying of hair"}]}},{"entity":"MGI:3834217","phenotype":{"types":[{"id":"MP:0002841","label":"impaired skeletal muscle contractility"}]}},{"entity":"ClinVarVariant:45379","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:158297","phenotype":{"types":[{"id":"HP:0010761","label":"Broad columella"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004470-WBRNAi00085516","phenotype":{"types":[{"id":"WBPhenotype:0001954","label":"diplotene absent during oogenesis"}]}},{"entity":"ClinVarVariant:7309","phenotype":{"types":[{"id":"HP:0000954","label":"Single transverse palmar crease"}]}},{"entity":"ClinVarVariant:11580","phenotype":{"types":[{"id":"HP:0002007","label":"Frontal bossing"}]}},{"entity":"ClinVarVariant:7057","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:10283","phenotype":{"types":[{"id":"HP:0100710","label":"Impulsivity"}]}},{"entity":"ClinVarVariant:8492","phenotype":{"types":[{"id":"HP:0001332","label":"Dystonia"}]}},{"entity":"MGI:3841488","phenotype":{"types":[{"id":"HP:0004324","label":"Increased body weight"}]}},{"entity":"ClinVarVariant:189720","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"MGI:5140883","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"MGI:2182765","phenotype":{"types":[{"id":"MP:0001257","label":"increased body length"}]}},{"entity":"ClinVarVariant:39667","phenotype":{"types":[{"id":"HP:0001067","label":"Neurofibromas"}]}},{"entity":"ClinVarVariant:690","phenotype":{"types":[{"id":"HP:0010471","label":"Oligosacchariduria"}]}},{"entity":"ClinVarVariant:38952","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:215911","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:143120","phenotype":{"types":[{"id":"HP:0001653","label":"Mitral regurgitation"}]}},{"entity":"ClinVarVariant:159945","phenotype":{"types":[{"id":"HP:0002465","label":"Poor speech"}]}},{"entity":"ClinVarVariant:45183","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"ClinVarVariant:66101","phenotype":{"types":[{"id":"HP:0004469","label":"Chronic bronchitis"}]}},{"entity":"ClinVarVariant:127491","phenotype":{"types":[{"id":"HP:0000377","label":"Abnormality of the pinna"}]}},{"entity":"ClinVarVariant:208829","phenotype":{"types":[{"id":"HP:0009601","label":"Aplasia/Hypoplasia of the thumb"}]}},{"entity":"ClinVarVariant:24772","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:36051","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:158343","phenotype":{"types":[{"id":"HP:0000742","label":"Self-mutilation"}]}},{"entity":"dbSNP:rs10172646","phenotype":{"types":[{"id":"HP:0001931","label":"Hypochromic anemia"}]}},{"entity":"ClinVarVariant:56735","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:162049","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:12595","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"ClinVarVariant:13342","phenotype":{"types":[{"id":"HP:0002861","label":"Melanoma"}]}},{"entity":"ClinVarVariant:184560","phenotype":{"types":[{"id":"HP:0009734","label":"Optic glioma"}]}},{"entity":"ClinVarVariant:5985","phenotype":{"types":[{"id":"HP:0003119","label":"Abnormality of lipid metabolism"}]}},{"entity":"ClinVarVariant:92534","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:17178","phenotype":{"types":[{"id":"HP:0006149","label":"Increased laxity of fingers"}]}},{"entity":"FlyBase:FBal0137361","phenotype":{"types":[{"id":"FBbt:00005634PHENOTYPE","label":"Drosophila embryonic Malpighian tubule phenotype"}]}},{"entity":"ClinVarVariant:99942","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"MGI:1891594","phenotype":{"types":[{"id":"HP:0008222","label":"Female infertility"}]}},{"entity":"ClinVarVariant:53953","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:64885","phenotype":{"types":[{"id":"HP:0003881","label":"Humeral sclerosis"}]}},{"entity":"ClinVarVariant:180352","phenotype":{"types":[{"id":"HP:0002835","label":"Aspiration"}]}},{"entity":"ClinVarVariant:2023","phenotype":{"types":[{"id":"HP:0000830","label":"Anterior hypopituitarism"}]}},{"entity":"ClinVarVariant:94505","phenotype":{"types":[{"id":"HP:0002948","label":"Vertebral fusion"}]}},{"entity":"ClinVarVariant:12048","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"AQTL:20712","phenotype":{"types":[{"id":"AQTLTrait:1114","label":"Body length"}]}},{"entity":"MGI:1932294","phenotype":{"types":[{"id":"HP:0012819","label":"Myocarditis"}]}},{"entity":"ClinVarVariant:12493","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"ClinVarVariant:12589","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:24660","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:48937","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:13960","phenotype":{"types":[{"id":"HP:0002208","label":"Coarse hair"}]}},{"entity":"ClinVarVariant:21062","phenotype":{"types":[{"id":"HP:0000660","label":"Lipemia retinalis"}]}},{"entity":"ClinVarVariant:158712","phenotype":{"types":[{"id":"HP:0009237","label":"Short 5th finger"}]}},{"entity":"ClinVarVariant:11931","phenotype":{"types":[{"id":"HP:0001376","label":"Limitation of joint mobility"}]}},{"entity":"ClinVarVariant:204128","phenotype":{"types":[{"id":"HP:0100758","label":"Gangrene"}]}},{"entity":"ClinVarVariant:35880","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:155757","phenotype":{"types":[{"id":"HP:0001539","label":"Omphalocele"}]}},{"entity":"FlyBase:FBal0298766","phenotype":{"types":[{"id":"FBbt:00007250PHENOTYPE","label":"Drosophila inter-ommatidial cell phenotype"}]}},{"entity":"ClinVarVariant:189801","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"ClinVarVariant:167312","phenotype":{"types":[{"id":"HP:0002027","label":"Abdominal pain"}]}},{"entity":"ClinVarVariant:159955","phenotype":{"types":[{"id":"HP:0002465","label":"Poor speech"}]}},{"entity":"ClinVarVariant:127747","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:373","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"MGI:1861456","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"FlyBase:FBal0150123","phenotype":{"types":[{"id":"FBbt:00004970PHENOTYPE","label":"cuticle phenotype"}]}},{"entity":"FlyBase:FBal0183487","phenotype":{"types":[{"id":"FBcv:0000430","label":"cell polarity defective"}]}},{"entity":"ClinVarVariant:11218","phenotype":{"types":[{"id":"HP:0001685","label":"Myocardial fibrosis"}]}},{"entity":"MGI:5311370","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"ClinVarVariant:10497","phenotype":{"types":[{"id":"HP:0011855","label":"Pharyngeal edema"}]}},{"entity":"ClinVarVariant:53319","phenotype":{"types":[{"id":"HP:0100027","label":"Recurrent pancreatitis"}]}},{"entity":"ClinVarVariant:49838","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:68576","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:10572","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"MGI:4454555","phenotype":{"types":[{"id":"MP:0001745","label":"increased circulating corticosterone level"}]}},{"entity":"ClinVarVariant:97593","phenotype":{"types":[{"id":"HP:0005214","label":"Intestinal obstruction"}]}},{"entity":"ClinVarVariant:161981","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"ClinVarVariant:40512","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:188788","phenotype":{"types":[{"id":"HP:0000649","label":"Abnormality of visual evoked potentials"}]}},{"entity":"ClinVarVariant:10174","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:38289","phenotype":{"types":[{"id":"HP:0002196","label":"Myelopathy"}]}},{"entity":"ClinVarVariant:2334","phenotype":{"types":[{"id":"HP:0001315","label":"Reduced tendon reflexes"}]}},{"entity":"ClinVarVariant:64739","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:177995","phenotype":{"types":[{"id":"HP:0001279","label":"Syncope"}]}},{"entity":"ClinVarVariant:53999","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:181735","phenotype":{"types":[{"id":"HP:0008572","label":"External ear malformation"}]}},{"entity":"ClinVarVariant:11712","phenotype":{"types":[{"id":"HP:0001388","label":"Joint laxity"}]}},{"entity":"ClinVarVariant:38324","phenotype":{"types":[{"id":"HP:0000046","label":"Scrotal hypoplasia"}]}},{"entity":"ClinVarVariant:11077","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:7151","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:9141","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:188928","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:9064","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017241-WBRNAi00096241","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-001103-2-ZDB-MRPHLNO-041110-4-ZDB-MRPHLNO-050322-1","phenotype":{"types":[{"id":"ZP:0000064","label":"abnormal(ly) decreased size ceratohyal cartilage"}]}},{"entity":"ClinVarVariant:40680","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:210726","phenotype":{"types":[{"id":"HP:0001231","label":"Abnormality of the fingernails"}]}},{"entity":"MGI:3584018","phenotype":{"types":[{"id":"HP:0100827","label":"Lymphocytosis"}]}},{"entity":"NCBIGene:100526741","phenotype":{"types":[{"id":"HP:0002823","label":"Abnormality of the femur"}]}},{"entity":"ClinVarVariant:42317","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"ClinVarVariant:12786","phenotype":{"types":[{"id":"HP:0001028","label":"Hemangioma"}]}},{"entity":"MGI:4450934","phenotype":{"types":[{"id":"MP:0002188","label":"small heart"}]}},{"entity":"ClinVarVariant:43594","phenotype":{"types":[{"id":"HP:0002488","label":"Acute leukemia"}]}},{"entity":"ClinVarVariant:211626","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"FlyBase:FBal0206465","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:159239","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:156048","phenotype":{"types":[{"id":"HP:0002270","label":"Abnormality of the autonomic nervous system"}]}},{"entity":"ClinVarVariant:24478","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:40565","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"dbSNP:rs41625970","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:1461","phenotype":{"types":[{"id":"HP:0007359","label":"Focal seizures"}]}},{"entity":"ClinVarVariant:9581","phenotype":{"types":[{"id":"HP:0002401","label":"Stroke-like episodes"}]}},{"entity":"ClinVarVariant:21170","phenotype":{"types":[{"id":"HP:0001511","label":"Intrauterine growth retardation"}]}},{"entity":"ClinVarVariant:189700","phenotype":{"types":[{"id":"HP:0000478","label":"Abnormality of the eye"}]}},{"entity":"ClinVarVariant:14067","phenotype":{"types":[{"id":"HP:0001712","label":"Left ventricular hypertrophy"}]}},{"entity":"ClinVarVariant:49844","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:36848","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:16901","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:100938","phenotype":{"types":[{"id":"HP:0007018","label":"Attention deficit hyperactivity disorder"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000817-WBRNAi00073502","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:46499","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"dbSNP:rs41597892","phenotype":{"types":[{"id":"AQTLTrait:1101","label":"Foot angle"}]}},{"entity":"ClinVarVariant:167132","phenotype":{"types":[{"id":"HP:0000225","label":"Gingival bleeding"}]}},{"entity":"FlyBase:FBal0151927","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"AQTL:33210","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001210-WBRNAi00090496","phenotype":{"types":[{"id":"WBPhenotype:0001645","label":"protein degradation variant"}]}},{"entity":"ClinVarVariant:94504","phenotype":{"types":[{"id":"HP:0008443","label":"Spinal deformities"}]}},{"entity":"ClinVarVariant:4950","phenotype":{"types":[{"id":"HP:0005855","label":"Multiple prenatal fractures"}]}},{"entity":"ClinVarVariant:3331","phenotype":{"types":[{"id":"HP:0001575","label":"Mood changes"}]}},{"entity":"ClinVarVariant:210258","phenotype":{"types":[{"id":"HP:0007360","label":"Aplasia/Hypoplasia of the cerebellum"}]}},{"entity":"ClinVarVariant:101203","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"AQTL:1008","phenotype":{"types":[{"id":"AQTLTrait:3088","label":"Shoulder muscle weight"}]}},{"entity":"ClinVarVariant:24227","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:6011","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:43690","phenotype":{"types":[{"id":"HP:0000268","label":"Dolichocephaly"}]}},{"entity":"FlyBase:FBal0237989","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"MGI:2180062","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:25201","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:142320","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:36061","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:180362","phenotype":{"types":[{"id":"HP:0002835","label":"Aspiration"}]}},{"entity":"MGI:5301308","phenotype":{"types":[{"id":"MP:0004810","label":"decreased hematopoietic stem cell number"}]}},{"entity":"ClinVarVariant:156447","phenotype":{"types":[{"id":"HP:0000138","label":"Ovarian cyst"}]}},{"entity":"ClinVarVariant:10905","phenotype":{"types":[{"id":"HP:0002716","label":"Lymphadenopathy"}]}},{"entity":"ClinVarVariant:94260","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:3282","phenotype":{"types":[{"id":"HP:0009588","label":"Vestibular Schwannoma"}]}},{"entity":"ClinVarVariant:65095","phenotype":{"types":[{"id":"HP:0009727","label":"Achromatic retinal patches"}]}},{"entity":"ClinVarVariant:30186","phenotype":{"types":[{"id":"HP:0100021","label":"Cerebral palsy"}]}},{"entity":"ClinVarVariant:607","phenotype":{"types":[{"id":"HP:0100753","label":"Schizophrenia"}]}},{"entity":"ZFIN:ZDB-ALT-070117-12","phenotype":{"types":[{"id":"ZP:0008988","label":"abnormal(ly) disrupted regulation of hydrogen peroxide metabolic process"}]}},{"entity":"FlyBase:FBal0318121","phenotype":{"types":[{"id":"FBbt:00000015PHENOTYPE","label":"Drosophila thorax phenotype"}]}},{"entity":"ClinVarVariant:9153","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"ClinVarVariant:2240","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"WormBase:WBVar00087821","phenotype":{"types":[{"id":"WBPhenotype:0001384","label":"fertility reduced"}]}},{"entity":"ClinVarVariant:466","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:53630","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:136044","phenotype":{"types":[{"id":"HP:0001587","label":"Primary ovarian failure"}]}},{"entity":"ClinVarVariant:137633","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"MGI:2386179","phenotype":{"types":[{"id":"HP:0012533","label":"Allodynia"}]}},{"entity":"ClinVarVariant:217059","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:137950","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"ClinVarVariant:18045","phenotype":{"types":[{"id":"HP:0004850","label":"Recurrent deep vein thrombosis"}]}},{"entity":"ClinVarVariant:4407","phenotype":{"types":[{"id":"HP:0002200","label":"Pseudobulbar signs"}]}},{"entity":"FlyBase:FBal0045026","phenotype":{"types":[{"id":"FBbt:00004223PHENOTYPE","label":"Drosophila photoreceptor cell R6 phenotype"}]}},{"entity":"ClinVarVariant:36948","phenotype":{"types":[{"id":"HP:0002206","label":"Pulmonary fibrosis"}]}},{"entity":"ClinVarVariant:161343","phenotype":{"types":[{"id":"HP:0001038","label":"Warfarin-induced skin necrosis"}]}},{"entity":"dbSNP:rs6538140","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"MGI:5449877","phenotype":{"types":[{"id":"HP:0002069","label":"Generalized tonic-clonic seizures"}]}},{"entity":"MGI:3845814","phenotype":{"types":[{"id":"MP:0010957","label":"abnormal aerobic respiration"}]}},{"entity":"ClinVarVariant:11369","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:2821","phenotype":{"types":[{"id":"HP:0007074","label":"Thick corpus callosum"}]}},{"entity":"ClinVarVariant:101186","phenotype":{"types":[{"id":"HP:0000387","label":"Absent earlobe"}]}},{"entity":"ClinVarVariant:6059","phenotype":{"types":[{"id":"HP:0003693","label":"Distal amyotrophy"}]}},{"entity":"dbSNP:rs81270306","phenotype":{"types":[{"id":"AQTLTrait:1023","label":"Hindquarter muscle weight"}]}},{"entity":"ClinVarVariant:18277","phenotype":{"types":[{"id":"HP:0002381","label":"Aphasia"}]}},{"entity":"ClinVarVariant:159096","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:41068","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:4394","phenotype":{"types":[{"id":"HP:0000540","label":"Hypermetropia"}]}},{"entity":"ClinVarVariant:12761","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:39786","phenotype":{"types":[{"id":"HP:0000414","label":"Bulbous nose"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004891-WBRNAi00083804","phenotype":{"types":[{"id":"WBPhenotype:0000812","label":"germ cell development variant"}]}},{"entity":"ClinVarVariant:55942","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:35849","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:156130","phenotype":{"types":[{"id":"HP:0010808","label":"Protruding tongue"}]}},{"entity":"FlyBase:FBal0154542","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:35845","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:65098","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:4943","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:41155","phenotype":{"types":[{"id":"HP:0000286","label":"Epicanthus"}]}},{"entity":"ClinVarVariant:10269","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:211718","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"ClinVarVariant:25026","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"ClinVarVariant:37090","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"WormBase:WBVar00248883","phenotype":{"types":[{"id":"WBPhenotype:0001744","label":"cell adhesion variant"}]}},{"entity":"FlyBase:FBal0042573","phenotype":{"types":[{"id":"FBbt:00005744PHENOTYPE","label":"Drosophila embryonic dorsal epidermis phenotype"}]}},{"entity":"ClinVarVariant:64739","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:35723","phenotype":{"types":[{"id":"HP:0000934","label":"Chondrocalcinosis"}]}},{"entity":"ClinVarVariant:94179","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"ClinVarVariant:18333","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"MGI:2156985","phenotype":{"types":[{"id":"MP:0002177","label":"abnormal outer ear morphology"}]}},{"entity":"ClinVarVariant:6717","phenotype":{"types":[{"id":"HP:0001900","label":"Increased hemoglobin"}]}},{"entity":"ClinVarVariant:139529","phenotype":{"types":[{"id":"HP:0000179","label":"Thick lower lip vermilion"}]}},{"entity":"ClinVarVariant:190378","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-040426-2906-ZDB-MRPHLNO-100915-2-ZDB-MRPHLNO-100915-3","phenotype":{"types":[{"id":"ZP:0000962","label":"abnormal(ly) disrupted axonal fasciculation"}]}},{"entity":"ClinVarVariant:189083","phenotype":{"types":[{"id":"HP:0000510","label":"Rod-cone dystrophy"}]}},{"entity":"ClinVarVariant:21255","phenotype":{"types":[{"id":"HP:0002797","label":"Osteolysis"}]}},{"entity":"ClinVarVariant:7215","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:49540","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:209029","phenotype":{"types":[{"id":"HP:0000777","label":"Abnormality of the thymus"}]}},{"entity":"ClinVarVariant:10313","phenotype":{"types":[{"id":"HP:0100309","label":"Subdural hemorrhage"}]}},{"entity":"MGI:5462249","phenotype":{"types":[{"id":"MP:0004532","label":"abnormal inner hair cell stereociliary bundle morphology"}]}},{"entity":"ClinVarVariant:158349","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:12844","phenotype":{"types":[{"id":"HP:0008341","label":"Distal renal tubular acidosis"}]}},{"entity":"FlyBase:FBal0052396","phenotype":{"types":[{"id":"FBbt:00000155PHENOTYPE","label":"Drosophila embryonic head phenotype"}]}},{"entity":"MGI:2180685","phenotype":{"types":[{"id":"MP:0005093","label":"decreased B cell proliferation"}]}},{"entity":"ClinVarVariant:188728","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:10748","phenotype":{"types":[{"id":"HP:0000763","label":"Sensory neuropathy"}]}},{"entity":"ClinVarVariant:24841","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:7750","phenotype":{"types":[{"id":"HP:0012062","label":"Bone cyst"}]}},{"entity":"MGI:4431694","phenotype":{"types":[{"id":"HP:0009887","label":"Abnormality of hair pigmentation"}]}},{"entity":"MGI:3037859","phenotype":{"types":[{"id":"MP:0001394","label":"circling"}]}},{"entity":"ClinVarVariant:40553","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:6927","phenotype":{"types":[{"id":"HP:0004416","label":"Precocious atherosclerosis"}]}},{"entity":"ClinVarVariant:13361","phenotype":{"types":[{"id":"HP:0009830","label":"Peripheral neuropathy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011480-WBRNAi00071460","phenotype":{"types":[{"id":"WBPhenotype:0001425","label":"receptor mediated endocytosis defective"}]}},{"entity":"NCBIGene:100187724","phenotype":{"types":[{"id":"HP:0001161","label":"Hand polydactyly"}]}},{"entity":"ClinVarVariant:189254","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:210769","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:159222","phenotype":{"types":[{"id":"HP:0011951","label":"Aspiration pneumonia"}]}},{"entity":"ClinVarVariant:198999","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"ClinVarVariant:126817","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:189603","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:136156","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:6551","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"ClinVarVariant:128454","phenotype":{"types":[{"id":"HP:0100579","label":"Mucosal telangiectasiae"}]}},{"entity":"ClinVarVariant:93346","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"WormBase:WBVar00090199","phenotype":{"types":[{"id":"WBPhenotype:0001221","label":"nose touch defective"}]}},{"entity":"ClinVarVariant:2141","phenotype":{"types":[{"id":"HP:0009829","label":"Phocomelia"}]}},{"entity":"ClinVarVariant:940","phenotype":{"types":[{"id":"HP:0003053","label":"Epiphyseal deformities of tubular bones"}]}},{"entity":"ClinVarVariant:53705","phenotype":{"types":[{"id":"HP:0004936","label":"Venous thrombosis"}]}},{"entity":"ClinVarVariant:204184","phenotype":{"types":[{"id":"HP:0012622","label":"Chronic kidney disease"}]}},{"entity":"ClinVarVariant:5396","phenotype":{"types":[{"id":"HP:0001655","label":"Patent foramen ovale"}]}},{"entity":"MGI:1934013","phenotype":{"types":[{"id":"MP:0008810","label":"increased circulating iron level"}]}},{"entity":"ClinVarVariant:50009","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:211665","phenotype":{"types":[{"id":"HP:0000413","label":"Atresia of the external auditory canal"}]}},{"entity":"ClinVarVariant:24243","phenotype":{"types":[{"id":"HP:0012622","label":"Chronic kidney disease"}]}},{"entity":"MGI:4836722","phenotype":{"types":[{"id":"HP:0040216","label":"Hypoinsulinemia"}]}},{"entity":"ClinVarVariant:159226","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:143858","phenotype":{"types":[{"id":"HP:0002376","label":"Developmental regression"}]}},{"entity":"FlyBase:FBal0285352","phenotype":{"types":[{"id":"FBbt:00004580PHENOTYPE","label":"Drosophila mesothoracic tergum phenotype"}]}},{"entity":"ClinVarVariant:101219","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:25321","phenotype":{"types":[{"id":"HP:0100626","label":"Chronic hepatic failure"}]}},{"entity":"MGI:3775093","phenotype":{"types":[{"id":"MP:0002052","label":"decreased tumor incidence"}]}},{"entity":"ClinVarVariant:143832","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000201-WBRNAi00088651","phenotype":{"types":[{"id":"WBPhenotype:0002057","label":"Bacillus thuringiensis toxin hypersensitive"}]}},{"entity":"MGI:5295482","phenotype":{"types":[{"id":"HP:0012447","label":"Abnormal myelination"}]}},{"entity":"ClinVarVariant:40243","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:188151","phenotype":{"types":[{"id":"HP:0002894","label":"Neoplasm of the pancreas"}]}},{"entity":"ClinVarVariant:16332","phenotype":{"types":[{"id":"HP:0003811","label":"Neonatal death"}]}},{"entity":"ClinVarVariant:24723","phenotype":{"types":[{"id":"HP:0030034","label":"Diffuse glomerular basement membrane lamellation"}]}},{"entity":"ClinVarVariant:82781","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"MGI:2384028","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:48104","phenotype":{"types":[{"id":"HP:0100272","label":"Branchial sinus"}]}},{"entity":"ClinVarVariant:2666","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:5849","phenotype":{"types":[{"id":"HP:0000684","label":"Delayed eruption of teeth"}]}},{"entity":"MGI:3047571","phenotype":{"types":[{"id":"MP:0008178","label":"decreased germinal center B cell number"}]}},{"entity":"ClinVarVariant:141579","phenotype":{"types":[{"id":"HP:0002216","label":"Premature graying of hair"}]}},{"entity":"ClinVarVariant:6395","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"AQTL:2263","phenotype":{"types":[{"id":"AQTLTrait:2048","label":"Drumstick weight"}]}},{"entity":"ClinVarVariant:158183","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"MGI:3575756","phenotype":{"types":[{"id":"MP:0001874","label":"acanthosis"}]}},{"entity":"ClinVarVariant:53638","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"FlyBase:FBal0297233","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:17494","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:5033","phenotype":{"types":[{"id":"HP:0003477","label":"Peripheral axonal neuropathy"}]}},{"entity":"ClinVarVariant:17370","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:190796","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"MGI:4839367","phenotype":{"types":[{"id":"MP:0009716","label":"abnormal subcommissural organ morphology"}]}},{"entity":"ClinVarVariant:135746","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:188246","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:53626","phenotype":{"types":[{"id":"HP:0006510","label":"Chronic obstructive pulmonary disease"}]}},{"entity":"ClinVarVariant:215765","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:88863","phenotype":{"types":[{"id":"HP:0011108","label":"Recurrent sinusitis"}]}},{"entity":"ClinVarVariant:67956","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:159118","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:21249","phenotype":{"types":[{"id":"HP:0006487","label":"Bowing of the long bones"}]}},{"entity":"ClinVarVariant:207996","phenotype":{"types":[{"id":"HP:0002749","label":"Osteomalacia"}]}},{"entity":"ClinVarVariant:215985","phenotype":{"types":[{"id":"HP:0000612","label":"Iris coloboma"}]}},{"entity":"ClinVarVariant:36081","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:97710","phenotype":{"types":[{"id":"HP:0001596","label":"Alopecia"}]}},{"entity":"FlyBase:FBal0242010","phenotype":{"types":[{"id":"FBbt:00006029PHENOTYPE","label":"Drosophila wing pouch phenotype"}]}},{"entity":"ClinVarVariant:41196","phenotype":{"types":[{"id":"HP:0010535","label":"Sleep apnea"}]}},{"entity":"ClinVarVariant:10136","phenotype":{"types":[{"id":"HP:0005261","label":"Joint hemorrhage"}]}},{"entity":"ClinVarVariant:189623","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"FlyBase:FBal0159231","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:4280","phenotype":{"types":[{"id":"HP:0001053","label":"Hypopigmented skin patches"}]}},{"entity":"ClinVarVariant:65546","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"MGI:1857691","phenotype":{"types":[{"id":"MP:0013216","label":"absent ectoderm"}]}},{"entity":"ClinVarVariant:53178","phenotype":{"types":[{"id":"HP:0100582","label":"Nasal polyposis"}]}},{"entity":"ClinVarVariant:24385","phenotype":{"types":[{"id":"HP:0000093","label":"Proteinuria"}]}},{"entity":"ClinVarVariant:92893","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:21402","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:188745","phenotype":{"types":[{"id":"HP:0001982","label":"Sea-blue histiocytosis"}]}},{"entity":"MGI:1857129","phenotype":{"types":[{"id":"MP:0005386","label":"behavior/neurological phenotype"}]}},{"entity":"ClinVarVariant:159897","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"dbSNP:rs41581462","phenotype":{"types":[{"id":"AQTLTrait:1173","label":"Rear leg set"}]}},{"entity":"ClinVarVariant:41182","phenotype":{"types":[{"id":"HP:0003162","label":"Fasting hypoglycemia"}]}},{"entity":"ClinVarVariant:36062","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:21585","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:210013","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:7112","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:101239","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:41354","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:42353","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"ZFIN:ZDB-ALT-040721-22","phenotype":{"types":[{"id":"ZP:0000100","label":"abnormal(ly) morphology brain"}]}},{"entity":"ClinVarVariant:24444","phenotype":{"types":[{"id":"HP:0007763","label":"Retinal telangiectasia"}]}},{"entity":"MGI:2179136","phenotype":{"types":[{"id":"MP:0006011","label":"abnormal endolymphatic duct morphology"}]}},{"entity":"ClinVarVariant:167477","phenotype":{"types":[{"id":"HP:0005576","label":"Tubulointerstitial fibrosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003834-WBRNAi00040618","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:127355","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"MGI:3609477","phenotype":{"types":[{"id":"MP:0002169","label":"no abnormal phenotype detected"}]}},{"entity":"ClinVarVariant:215464","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"ClinVarVariant:36082","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"MGI:2158467","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:8880","phenotype":{"types":[{"id":"HP:0000863","label":"Central diabetes insipidus"}]}},{"entity":"ClinVarVariant:202211","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ClinVarVariant:48035","phenotype":{"types":[{"id":"HP:0003198","label":"Myopathy"}]}},{"entity":"MGI:1857117","phenotype":{"types":[{"id":"HP:0000961","label":"Cyanosis"}]}},{"entity":"ClinVarVariant:7175","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"MGI:1861705","phenotype":{"types":[{"id":"MP:0000133","label":"abnormal long bone metaphysis morphology"}]}},{"entity":"ZFIN:ZDB-ALT-150203-1","phenotype":{"types":[{"id":"ZP:0012596","label":"abnormal(ly) has extra parts of type compact layer of ventricle basal cortex towards compact layer of ventricle cardiac myofibril"}]}},{"entity":"ClinVarVariant:38975","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:38321","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"FlyBase:FBal0124001","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:143788","phenotype":{"types":[{"id":"HP:0000478","label":"Abnormality of the eye"}]}},{"entity":"ClinVarVariant:36072","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:100921","phenotype":{"types":[{"id":"HP:0007359","label":"Focal seizures"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00016117-WBRNAi00027443","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:211667","phenotype":{"types":[{"id":"HP:0000776","label":"Congenital diaphragmatic hernia"}]}},{"entity":"MGI:2388372","phenotype":{"types":[{"id":"HP:0001941","label":"Acidosis"}]}},{"entity":"ClinVarVariant:190366","phenotype":{"types":[{"id":"HP:0002493","label":"Upper motor neuron dysfunction"}]}},{"entity":"ClinVarVariant:5710","phenotype":{"types":[{"id":"HP:0002179","label":"Opisthotonus"}]}},{"entity":"ClinVarVariant:8470","phenotype":{"types":[{"id":"HP:0003551","label":"Difficulty climbing stairs"}]}},{"entity":"MGI:3775302","phenotype":{"types":[{"id":"HP:0010783","label":"Erythema"}]}},{"entity":"OMIM:242840","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"MGI:4949192","phenotype":{"types":[{"id":"HP:0002242","label":"Abnormality of the intestine"}]}},{"entity":"AQTL:32413","phenotype":{"types":[{"id":"AQTLTrait:1004","label":"Somatic cell count"}]}},{"entity":"ClinVarVariant:66013","phenotype":{"types":[{"id":"HP:0001075","label":"Atrophic scars"}]}},{"entity":"ClinVarVariant:24976","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:31196","phenotype":{"types":[{"id":"HP:0003805","label":"Rimmed vacuoles"}]}},{"entity":"ClinVarVariant:52358","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:162065","phenotype":{"types":[{"id":"HP:0009773","label":"Symphalangism affecting the phalanges of the hand"}]}},{"entity":"ClinVarVariant:197868","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"MGI:2663662","phenotype":{"types":[{"id":"HP:0001875","label":"Neutropenia"}]}},{"entity":"ClinVarVariant:3296","phenotype":{"types":[{"id":"HP:0008069","label":"Neoplasm of the skin"}]}},{"entity":"MGI:4999600","phenotype":{"types":[{"id":"MP:0004971","label":"dermal hyperplasia"}]}},{"entity":"FlyBase:FBal0207033","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:11510","phenotype":{"types":[{"id":"HP:0002938","label":"Lumbar hyperlordosis"}]}},{"entity":"ClinVarVariant:29737","phenotype":{"types":[{"id":"HP:0000602","label":"Ophthalmoplegia"}]}},{"entity":"ClinVarVariant:53902","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00015538-WBRNAi00027160","phenotype":{"types":[{"id":"WBPhenotype:0000697","label":"protruding vulva"}]}},{"entity":"ClinVarVariant:53905","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:36042","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:14889","phenotype":{"types":[{"id":"HP:0008740","label":"Longitudinal vaginal septum"}]}},{"entity":"ClinVarVariant:65064","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"FlyBase:FBal0210388","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:41141","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:10589","phenotype":{"types":[{"id":"HP:0100845","label":"Anaphylactic shock"}]}},{"entity":"ClinVarVariant:12464","phenotype":{"types":[{"id":"HP:0002058","label":"Myopathic facies"}]}},{"entity":"ClinVarVariant:8240","phenotype":{"types":[{"id":"HP:0008947","label":"Infantile muscular hypotonia"}]}},{"entity":"ClinVarVariant:135755","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:210036","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"FlyBase:FBal0240836","phenotype":{"types":[{"id":"FBbt:00004930PHENOTYPE","label":"hub cell phenotype"}]}},{"entity":"dbSNP:rs826221","phenotype":{"types":[{"id":"HP:0002063","label":"Rigidity"}]}},{"entity":"ClinVarVariant:181725","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:161997","phenotype":{"types":[{"id":"HP:0006280","label":"Chronic pancreatitis"}]}},{"entity":"ClinVarVariant:25370","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"dbSNP:rs4869931","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"ClinVarVariant:35870","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"MGI:3530536","phenotype":{"types":[{"id":"MP:0001475","label":"reduced long term depression"}]}},{"entity":"ClinVarVariant:5343","phenotype":{"types":[{"id":"HP:0000968","label":"Ectodermal dysplasia"}]}},{"entity":"MGI:4459078","phenotype":{"types":[{"id":"MP:0010053","label":"decreased grip strength"}]}},{"entity":"ClinVarVariant:132900","phenotype":{"types":[{"id":"HP:0000726","label":"Dementia"}]}},{"entity":"ClinVarVariant:35666","phenotype":{"types":[{"id":"HP:0100530","label":"Abnormality of calcium-phosphate metabolism"}]}},{"entity":"ClinVarVariant:159961","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ClinVarVariant:159118","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"MGI:2154514","phenotype":{"types":[{"id":"HP:0008516","label":"Abnormality of the vertebral spinous processes"}]}},{"entity":"ClinVarVariant:67814","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:840","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:127737","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:24696","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"ClinVarVariant:102431","phenotype":{"types":[{"id":"HP:0001800","label":"Hypoplastic toenails"}]}},{"entity":"MGI:1857257","phenotype":{"types":[{"id":"MP:0008214","label":"increased immature B cell number"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000066-WBRNAi00095708","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:36052","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:11520","phenotype":{"types":[{"id":"HP:0002938","label":"Lumbar hyperlordosis"}]}},{"entity":"ClinVarVariant:163758","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:127415","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:159007","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:9694","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"FlyBase:FBal0305269","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:5616","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:35865","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:43212","phenotype":{"types":[{"id":"HP:0000360","label":"Tinnitus"}]}},{"entity":"ClinVarVariant:24528","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:96387","phenotype":{"types":[{"id":"HP:0100720","label":"Hypoplasia of the ear cartilage"}]}},{"entity":"AQTL:27380","phenotype":{"types":[{"id":"AQTLTrait:1485","label":"Mean corpuscular volume"}]}},{"entity":"ClinVarVariant:156068","phenotype":{"types":[{"id":"HP:0002270","label":"Abnormality of the autonomic nervous system"}]}},{"entity":"ClinVarVariant:210773","phenotype":{"types":[{"id":"HP:0010562","label":"Keloids"}]}},{"entity":"ClinVarVariant:188044","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"FlyBase:FBal0249096","phenotype":{"types":[{"id":"FBbt:00100216PHENOTYPE","label":"dopaminergic PPM1 neuron phenotype"}]}},{"entity":"ClinVarVariant:197559","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:36963","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"dbSNP:rs80879875","phenotype":{"types":[{"id":"AQTLTrait:456","label":"Hemoglobin"}]}},{"entity":"ClinVarVariant:7442","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"MGI:3053810","phenotype":{"types":[{"id":"MP:0002404","label":"increased intestinal adenoma incidence"}]}},{"entity":"ClinVarVariant:190185","phenotype":{"types":[{"id":"HP:0002282","label":"Heterotopia"}]}},{"entity":"ClinVarVariant:138714","phenotype":{"types":[{"id":"HP:0200134","label":"Epileptic encephalopathy"}]}},{"entity":"ClinVarVariant:184231","phenotype":{"types":[{"id":"HP:0001376","label":"Limitation of joint mobility"}]}},{"entity":"ClinVarVariant:2915","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:29732","phenotype":{"types":[{"id":"HP:0002126","label":"Polymicrogyria"}]}},{"entity":"ClinVarVariant:54023","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:143714","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ZFIN:ZDB-ALT-060519-4","phenotype":{"types":[{"id":"ZP:0000041","label":"abnormal(ly) quality pharyngeal arch 3-7 skeleton"}]}},{"entity":"ClinVarVariant:24765","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:2666","phenotype":{"types":[{"id":"HP:0012368","label":"Flat face"}]}},{"entity":"ClinVarVariant:184969","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"ClinVarVariant:7935","phenotype":{"types":[{"id":"HP:0000077","label":"Abnormality of the kidney"}]}},{"entity":"ZFIN:ZDB-ALT-090424-3","phenotype":{"types":[{"id":"ZP:0008370","label":"abnormal(ly) absent gall bladder"}]}},{"entity":"ClinVarVariant:180710","phenotype":{"types":[{"id":"HP:0002151","label":"Increased serum lactate"}]}},{"entity":"ClinVarVariant:8427","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:156391","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:159254","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:31650","phenotype":{"types":[{"id":"HP:0001822","label":"Hallux valgus"}]}},{"entity":"AQTL:20631","phenotype":{"types":[{"id":"AQTLTrait:1112","label":"Withers height"}]}},{"entity":"ClinVarVariant:94585","phenotype":{"types":[{"id":"HP:0002948","label":"Vertebral fusion"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00018782-WBRNAi00099196","phenotype":{"types":[{"id":"WBPhenotype:0000961","label":"pattern of transgene expression variant"}]}},{"entity":"ClinVarVariant:159248","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"ClinVarVariant:160328","phenotype":{"types":[{"id":"HP:0001642","label":"Pulmonic stenosis"}]}},{"entity":"MGI:3832569","phenotype":{"types":[{"id":"MP:0006057","label":"decreased vascular endothelial cell number"}]}},{"entity":"ClinVarVariant:39111","phenotype":{"types":[{"id":"HP:0002721","label":"Immunodeficiency"}]}},{"entity":"ClinVarVariant:9106","phenotype":{"types":[{"id":"HP:0100615","label":"Ovarian neoplasm"}]}},{"entity":"ClinVarVariant:24697","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"MGI:1889550","phenotype":{"types":[{"id":"HP:0003826","label":"Stillbirth"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006768-WBRNAi00071339","phenotype":{"types":[{"id":"WBPhenotype:0000961","label":"pattern of transgene expression variant"}]}},{"entity":"ClinVarVariant:67947","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:53687","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:210474","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:49284","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:10935","phenotype":{"types":[{"id":"HP:0002716","label":"Lymphadenopathy"}]}},{"entity":"ClinVarVariant:13080","phenotype":{"types":[{"id":"HP:0002893","label":"Pituitary adenoma"}]}},{"entity":"_:genid1976017","phenotype":{"types":[{"id":"ZP:0003327","label":"abnormal(ly) disrupted cerebellum development"}]}},{"entity":"ClinVarVariant:189613","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"FlyBase:FBal0199281","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:156327","phenotype":{"types":[{"id":"HP:0006530","label":"Interstitial pulmonary disease"}]}},{"entity":"ClinVarVariant:11352","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"ClinVarVariant:102703","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:40512","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"ClinVarVariant:6433","phenotype":{"types":[{"id":"HP:0001939","label":"Abnormality of metabolism/homeostasis"}]}},{"entity":"ClinVarVariant:49241","phenotype":{"types":[{"id":"HP:0002103","label":"Abnormality of the pleura"}]}},{"entity":"ClinVarVariant:135779","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:56679","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:42900","phenotype":{"types":[{"id":"HP:0003128","label":"Lactic acidosis"}]}},{"entity":"ClinVarVariant:1175","phenotype":{"types":[{"id":"HP:0000013","label":"Hypoplasia of the uterus"}]}},{"entity":"ClinVarVariant:374","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"MGI:3709886","phenotype":{"types":[{"id":"HP:0011014","label":"Abnormal glucose homeostasis"}]}},{"entity":"ClinVarVariant:159181","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"dbSNP:rs29026584","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:65536","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:210471","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:53861","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:29690","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:3231","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"dbSNP:rs1768208","phenotype":{"types":[{"id":"HP:0000658","label":"Eyelid apraxia"}]}},{"entity":"ClinVarVariant:190356","phenotype":{"types":[{"id":"HP:0002493","label":"Upper motor neuron dysfunction"}]}},{"entity":"ClinVarVariant:5353","phenotype":{"types":[{"id":"HP:0001871","label":"Abnormality of blood and blood-forming tissues"}]}},{"entity":"ClinVarVariant:188802","phenotype":{"types":[{"id":"HP:0002487","label":"Hyperkinesis"}]}},{"entity":"ClinVarVariant:49761","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:30471","phenotype":{"types":[{"id":"HP:0004348","label":"Abnormality of bone mineral density"}]}},{"entity":"ClinVarVariant:36032","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-980526-332-ZDB-MRPHLNO-041217-12-ZDB-MRPHLNO-041217-13","phenotype":{"types":[{"id":"ZP:0000027","label":"abnormal(ly) decreased length post-vent region"}]}},{"entity":"ClinVarVariant:7235","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:54083","phenotype":{"types":[{"id":"HP:0000966","label":"Hypohidrosis"}]}},{"entity":"ClinVarVariant:97711","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"ClinVarVariant:159931","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:13090","phenotype":{"types":[{"id":"HP:0002893","label":"Pituitary adenoma"}]}},{"entity":"ClinVarVariant:8120","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:24856","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ClinVarVariant:5825","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:50191","phenotype":{"types":[{"id":"HP:0006772","label":"Renal angiomyolipoma"}]}},{"entity":"ClinVarVariant:2131","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:11161","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"MGI:3579497","phenotype":{"types":[{"id":"GO:0030154PHENOTYPE","label":"cell differentiation phenotype"}]}},{"entity":"AQTL:46070","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:136410","phenotype":{"types":[{"id":"HP:0200040","label":"Epidermoid cyst"}]}},{"entity":"AQTL:5491","phenotype":{"types":[{"id":"AQTLTrait:479","label":"Basophil number"}]}},{"entity":"dbSNP:rs110865743","phenotype":{"types":[{"id":"AQTLTrait:1004","label":"Somatic cell count"}]}},{"entity":"ClinVarVariant:198054","phenotype":{"types":[{"id":"HP:0011712","label":"Right bundle branch block"}]}},{"entity":"ClinVarVariant:13445","phenotype":{"types":[{"id":"HP:0001269","label":"Hemiparesis"}]}},{"entity":"ClinVarVariant:102806","phenotype":{"types":[{"id":"HP:0003231","label":"Hypertyrosinemia"}]}},{"entity":"ClinVarVariant:2657","phenotype":{"types":[{"id":"HP:0006101","label":"Finger syndactyly"}]}},{"entity":"ClinVarVariant:42307","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"ClinVarVariant:158297","phenotype":{"types":[{"id":"HP:0009911","label":"Abnormality of the temporal bone"}]}},{"entity":"ClinVarVariant:128211","phenotype":{"types":[{"id":"HP:0002488","label":"Acute leukemia"}]}},{"entity":"ClinVarVariant:9290","phenotype":{"types":[{"id":"HP:0002063","label":"Rigidity"}]}},{"entity":"ClinVarVariant:188893","phenotype":{"types":[{"id":"HP:0001947","label":"Renal tubular acidosis"}]}},{"entity":"ClinVarVariant:16788","phenotype":{"types":[{"id":"HP:0001274","label":"Agenesis of corpus callosum"}]}},{"entity":"MGI:2384513","phenotype":{"types":[{"id":"MP:0013184","label":"hemorrhagic ascites"}]}},{"entity":"AQTL:50226","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004460-WBRNAi00085472","phenotype":{"types":[{"id":"WBPhenotype:0001948","label":"diakinesis progression during oogenesis variant"}]}},{"entity":"ClinVarVariant:159180","phenotype":{"types":[{"id":"HP:0011951","label":"Aspiration pneumonia"}]}},{"entity":"FlyBase:FBal0040484","phenotype":{"types":[{"id":"FBbt:00004510PHENOTYPE","label":"Drosophila ommatidium phenotype"}]}},{"entity":"ClinVarVariant:8942","phenotype":{"types":[{"id":"HP:0100843","label":"Glioblastoma"}]}},{"entity":"ClinVarVariant:10100","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"MGI:3722325","phenotype":{"types":[{"id":"HP:0010772","label":"Anomalous pulmonary venous return"}]}},{"entity":"ClinVarVariant:49728","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:192299","phenotype":{"types":[{"id":"HP:0030034","label":"Diffuse glomerular basement membrane lamellation"}]}},{"entity":"ClinVarVariant:21101","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"ClinVarVariant:101229","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:10624","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"ClinVarVariant:12870","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:53975","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:6121","phenotype":{"types":[{"id":"HP:0003537","label":"Hypouricemia"}]}},{"entity":"MGI:1856173","phenotype":{"types":[{"id":"MP:0006030","label":"abnormal otic vesicle development"}]}},{"entity":"MGI:1857278","phenotype":{"types":[{"id":"HP:0000110","label":"Renal dysplasia"}]}},{"entity":"ClinVarVariant:212733","phenotype":{"types":[{"id":"HP:0100783","label":"Breast aplasia"}]}},{"entity":"ClinVarVariant:1902","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"ClinVarVariant:186916","phenotype":{"types":[{"id":"HP:0002858","label":"Meningioma"}]}},{"entity":"ClinVarVariant:94841","phenotype":{"types":[{"id":"HP:0003713","label":"Muscle fiber necrosis"}]}},{"entity":"ZFIN:ZDB-ALT-980520-19","phenotype":{"types":[{"id":"ZP:0000406","label":"abnormal(ly) quality sensory system"}]}},{"entity":"ClinVarVariant:9591","phenotype":{"types":[{"id":"HP:0002401","label":"Stroke-like episodes"}]}},{"entity":"ClinVarVariant:65859","phenotype":{"types":[{"id":"HP:0001182","label":"Tapered finger"}]}},{"entity":"ClinVarVariant:83189","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"ClinVarVariant:41057","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:64708","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"ClinVarVariant:209","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:182730","phenotype":{"types":[{"id":"HP:0003189","label":"Long nose"}]}},{"entity":"ClinVarVariant:41023","phenotype":{"types":[{"id":"HP:0009027","label":"Foot dorsiflexor weakness"}]}},{"entity":"ClinVarVariant:127338","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"ClinVarVariant:49450","phenotype":{"types":[{"id":"HP:0009719","label":"Hypomelanotic macule"}]}},{"entity":"ClinVarVariant:190346","phenotype":{"types":[{"id":"HP:0002493","label":"Upper motor neuron dysfunction"}]}},{"entity":"ClinVarVariant:3852","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"MGI:3779080","phenotype":{"types":[{"id":"MP:0010955","label":"abnormal respiratory electron transport chain"}]}},{"entity":"ClinVarVariant:216221","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:40563","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:35855","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"MGI:5635433","phenotype":{"types":[{"id":"MP:0004799","label":"increased susceptibility to experimental autoimmune encephalomyelitis"}]}},{"entity":"ClinVarVariant:24381","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"ClinVarVariant:35868","phenotype":{"types":[{"id":"HP:0100027","label":"Recurrent pancreatitis"}]}},{"entity":"ClinVarVariant:127830","phenotype":{"types":[{"id":"HP:0100585","label":"Telangiectasia of the skin"}]}},{"entity":"ClinVarVariant:143704","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ClinVarVariant:194332","phenotype":{"types":[{"id":"HP:0001350","label":"Slurred speech"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006944-WBRNAi00063314","phenotype":{"types":[{"id":"WBPhenotype:0000697","label":"protruding vulva"}]}},{"entity":"ClinVarVariant:3968","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"MGI:2677631","phenotype":{"types":[{"id":"HP:0010831","label":"Impaired proprioception"}]}},{"entity":"ClinVarVariant:4417","phenotype":{"types":[{"id":"HP:0002200","label":"Pseudobulbar signs"}]}},{"entity":"ClinVarVariant:53996","phenotype":{"types":[{"id":"HP:0010444","label":"Pulmonary insufficiency"}]}},{"entity":"ClinVarVariant:53726","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:25179","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:128201","phenotype":{"types":[{"id":"HP:0002488","label":"Acute leukemia"}]}},{"entity":"ClinVarVariant:207995","phenotype":{"types":[{"id":"HP:0002148","label":"Hypophosphatemia"}]}},{"entity":"MGI:5447471","phenotype":{"types":[{"id":"HP:0003097","label":"Short femur"}]}},{"entity":"ClinVarVariant:194115","phenotype":{"types":[{"id":"HP:0000232","label":"Everted lower lip vermilion"}]}},{"entity":"FlyBase:FBal0245644","phenotype":{"types":[{"id":"FBbt:00005378PHENOTYPE","label":"wing margin phenotype"}]}},{"entity":"FlyBase:FBal0125399","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:159093","phenotype":{"types":[{"id":"HP:0009937","label":"Facial hirsutism"}]}},{"entity":"ClinVarVariant:36093","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:209200","phenotype":{"types":[{"id":"HP:0002126","label":"Polymicrogyria"}]}},{"entity":"ClinVarVariant:12662","phenotype":{"types":[{"id":"HP:0000963","label":"Thin skin"}]}},{"entity":"ClinVarVariant:17247","phenotype":{"types":[{"id":"HP:0000772","label":"Abnormality of the ribs"}]}},{"entity":"ClinVarVariant:1589","phenotype":{"types":[{"id":"HP:0000140","label":"Abnormality of the menstrual cycle"}]}},{"entity":"ClinVarVariant:143113","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:6982","phenotype":{"types":[{"id":"HP:0002553","label":"Highly arched eyebrow"}]}},{"entity":"MGI:3711006","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:60534","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:143554","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"ClinVarVariant:56304","phenotype":{"types":[{"id":"HP:0001562","label":"Oligohydramnios"}]}},{"entity":"ClinVarVariant:10771","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:135886","phenotype":{"types":[{"id":"HP:0200042","label":"Skin ulcer"}]}},{"entity":"ClinVarVariant:101395","phenotype":{"types":[{"id":"HP:0005293","label":"Venous insufficiency"}]}},{"entity":"ClinVarVariant:38580","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"ClinVarVariant:10663","phenotype":{"types":[{"id":"HP:0005542","label":"Prolonged whole-blood clotting time"}]}},{"entity":"FlyBase:FBal0210316","phenotype":{"types":[{"id":"FBbt:00005149PHENOTYPE","label":"ganglion mother cell phenotype"}]}},{"entity":"ClinVarVariant:24412","phenotype":{"types":[{"id":"HP:0011508","label":"Macular hole"}]}},{"entity":"ClinVarVariant:4452","phenotype":{"types":[{"id":"HP:0001947","label":"Renal tubular acidosis"}]}},{"entity":"ClinVarVariant:156058","phenotype":{"types":[{"id":"HP:0002270","label":"Abnormality of the autonomic nervous system"}]}},{"entity":"ClinVarVariant:209163","phenotype":{"types":[{"id":"HP:0011220","label":"Prominent forehead"}]}},{"entity":"ClinVarVariant:7995","phenotype":{"types":[{"id":"HP:0002984","label":"Hypoplasia of the radius"}]}},{"entity":"ClinVarVariant:102626","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:10639","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"MGI:1856088","phenotype":{"types":[{"id":"MP:0006069","label":"abnormal retinal neuronal layer morphology"}]}},{"entity":"ClinVarVariant:7225","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:140867","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:36071","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:40370","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:11034","phenotype":{"types":[{"id":"HP:0001106","label":"Periorbital hyperpigmentation"}]}},{"entity":"ClinVarVariant:17219","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"MGI:3808477","phenotype":{"types":[{"id":"MP:0004920","label":"increased placenta weight"}]}},{"entity":"MGI:2183509","phenotype":{"types":[{"id":"MP:0004411","label":"decreased endocochlear potential"}]}},{"entity":"FlyBase:FBal0294937","phenotype":{"types":[{"id":"FBcv:0000440","label":"chemical sensitive"}]}},{"entity":"MGI:1857225","phenotype":{"types":[{"id":"MP:0004417","label":"decreased cochlear nerve compound action potential"}]}},{"entity":"ClinVarVariant:29700","phenotype":{"types":[{"id":"HP:0005900","label":"Fifth metacarpal with ulnar notch"}]}},{"entity":"ClinVarVariant:13070","phenotype":{"types":[{"id":"HP:0002893","label":"Pituitary adenoma"}]}},{"entity":"ClinVarVariant:21441","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:7179","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050103-13-ZDB-MRPHLNO-120727-1","phenotype":{"types":[{"id":"ZP:0002751","label":"abnormal(ly) hemorrhagic cranial vasculature"}]}},{"entity":"ClinVarVariant:211839","phenotype":{"types":[{"id":"HP:0007359","label":"Focal seizures"}]}},{"entity":"ClinVarVariant:65511","phenotype":{"types":[{"id":"HP:0002066","label":"Gait ataxia"}]}},{"entity":"ClinVarVariant:4465","phenotype":{"types":[{"id":"HP:0000988","label":"Skin rash"}]}},{"entity":"MGI:3852440","phenotype":{"types":[{"id":"MP:0010589","label":"common truncal valve"}]}},{"entity":"ClinVarVariant:195052","phenotype":{"types":[{"id":"HP:0004280","label":"Irregular ossification of hand bones"}]}},{"entity":"ClinVarVariant:56495","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:97701","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"ClinVarVariant:143714","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:2677647","phenotype":{"types":[{"id":"MP:0011088","label":"neonatal lethality, incomplete penetrance"}]}},{"entity":"ClinVarVariant:13396","phenotype":{"types":[{"id":"HP:0001260","label":"Dysarthria"}]}},{"entity":"ClinVarVariant:159973","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"ClinVarVariant:30664","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:31028","phenotype":{"types":[{"id":"HP:0010307","label":"Stridor"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006416-WBRNAi00095532","phenotype":{"types":[{"id":"WBPhenotype:0000402","label":"avoids bacterial lawn"}]}},{"entity":"ClinVarVariant:186867","phenotype":{"types":[{"id":"HP:0002073","label":"Progressive cerebellar ataxia"}]}},{"entity":"ClinVarVariant:11708","phenotype":{"types":[{"id":"HP:0008388","label":"Abnormality of the toenails"}]}},{"entity":"ClinVarVariant:36642","phenotype":{"types":[{"id":"HP:0004308","label":"Ventricular arrhythmia"}]}},{"entity":"ClinVarVariant:8965","phenotype":{"types":[{"id":"HP:0006561","label":"Lipid accumulation in hepatocytes"}]}},{"entity":"ClinVarVariant:25194","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:529","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"ClinVarVariant:156088","phenotype":{"types":[{"id":"HP:0002270","label":"Abnormality of the autonomic nervous system"}]}},{"entity":"ClinVarVariant:6111","phenotype":{"types":[{"id":"HP:0003537","label":"Hypouricemia"}]}},{"entity":"ClinVarVariant:189781","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ClinVarVariant:53484","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:53922","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"_:genid1976433","phenotype":{"types":[{"id":"ZP:0007732","label":"abnormal(ly) decreased amount skeletal muscle cell Z disc"}]}},{"entity":"ClinVarVariant:6718","phenotype":{"types":[{"id":"HP:0100587","label":"Abnormality of the preputium"}]}},{"entity":"ClinVarVariant:35755","phenotype":{"types":[{"id":"HP:0000137","label":"Abnormality of the ovary"}]}},{"entity":"ClinVarVariant:50081","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:1216","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"ClinVarVariant:137994","phenotype":{"types":[{"id":"HP:0000707","label":"Abnormality of the nervous system"}]}},{"entity":"ClinVarVariant:7142","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:10462","phenotype":{"types":[{"id":"HP:0003651","label":"Foam cells"}]}},{"entity":"ClinVarVariant:12063","phenotype":{"types":[{"id":"HP:0008321","label":"Reduced factor X activity"}]}},{"entity":"ClinVarVariant:2468","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:95939","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:39712","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004197-WBRNAi00007235","phenotype":{"types":[{"id":"WBPhenotype:0001263","label":"peroxisome morphology variant"}]}},{"entity":"ClinVarVariant:65124","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:215578","phenotype":{"types":[{"id":"HP:0008348","label":"Immunoglobulin IgG2 deficiency"}]}},{"entity":"ClinVarVariant:156238","phenotype":{"types":[{"id":"HP:0000496","label":"Abnormality of eye movement"}]}},{"entity":"ClinVarVariant:10279","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"AQTL:49858","phenotype":{"types":[{"id":"AQTLTrait:1004","label":"Somatic cell count"}]}},{"entity":"ClinVarVariant:48885","phenotype":{"types":[{"id":"HP:0100764","label":"Lymphangioma"}]}},{"entity":"FlyBase:FBal0236318","phenotype":{"types":[{"id":"FBbt:00000034PHENOTYPE","label":"Drosophila egg phenotype"}]}},{"entity":"ClinVarVariant:634","phenotype":{"types":[{"id":"HP:0004395","label":"Malnutrition"}]}},{"entity":"ClinVarVariant:6094","phenotype":{"types":[{"id":"HP:0006989","label":"Dysplastic corpus callosum"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001093-WBRNAi00026282","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:1932","phenotype":{"types":[{"id":"HP:0006573","label":"Acute hepatic steatosis"}]}},{"entity":"ClinVarVariant:2239","phenotype":{"types":[{"id":"HP:0001287","label":"Meningitis"}]}},{"entity":"ClinVarVariant:2020","phenotype":{"types":[{"id":"HP:0000992","label":"Cutaneous photosensitivity"}]}},{"entity":"ClinVarVariant:42391","phenotype":{"types":[{"id":"HP:0100775","label":"Dural ectasia"}]}},{"entity":"ClinVarVariant:48971","phenotype":{"types":[{"id":"HP:0009594","label":"Retinal hamartoma"}]}},{"entity":"MGI:1857149","phenotype":{"types":[{"id":"MP:0001191","label":"abnormal skin condition"}]}},{"entity":"ClinVarVariant:199656","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"ClinVarVariant:2824","phenotype":{"types":[{"id":"HP:0000297","label":"Facial hypotonia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022042-WBRNAi00081339","phenotype":{"types":[{"id":"WBPhenotype:0001027","label":"nuclear position defective early emb"}]}},{"entity":"ClinVarVariant:53705","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"MGI:4437094","phenotype":{"types":[{"id":"MP:0003059","label":"decreased insulin secretion"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004738-WBRNAi00065884","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:94537","phenotype":{"types":[{"id":"HP:0100595","label":"Camptocormia"}]}},{"entity":"ClinVarVariant:53663","phenotype":{"types":[{"id":"HP:0100651","label":"Type I diabetes mellitus"}]}},{"entity":"ClinVarVariant:136120","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:162048","phenotype":{"types":[{"id":"HP:0009830","label":"Peripheral neuropathy"}]}},{"entity":"ClinVarVariant:49800","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:39534","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:183820","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"MGI:1857227","phenotype":{"types":[{"id":"MP:0001921","label":"reduced fertility"}]}},{"entity":"ClinVarVariant:54030","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"ClinVarVariant:204016","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:2276","phenotype":{"types":[{"id":"HP:0002936","label":"Distal sensory impairment"}]}},{"entity":"ClinVarVariant:25211","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"MGI:2675121","phenotype":{"types":[{"id":"MP:0010979","label":"small ureteric bud"}]}},{"entity":"ClinVarVariant:11544","phenotype":{"types":[{"id":"HP:0006145","label":"Central Y-shaped metacarpal"}]}},{"entity":"ClinVarVariant:38302","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:161353","phenotype":{"types":[{"id":"HP:0001038","label":"Warfarin-induced skin necrosis"}]}},{"entity":"ClinVarVariant:5539","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"MGI:3583735","phenotype":{"types":[{"id":"MP:0000968","label":"abnormal sensory neuron innervation pattern"}]}},{"entity":"ClinVarVariant:11634","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"ZFIN:ZDB-ALT-050916-14","phenotype":{"types":[{"id":"ZP:0000530","label":"abnormal(ly) collapsed dorsal aorta"}]}},{"entity":"MGI:2156622","phenotype":{"types":[{"id":"MP:0001853","label":"heart inflammation"}]}},{"entity":"MGI:3578655","phenotype":{"types":[{"id":"GO:0021636PHENOTYPE","label":"trigeminal nerve morphogenesis phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004915-WBRNAi00075315","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:41172","phenotype":{"types":[{"id":"HP:0003162","label":"Fasting hypoglycemia"}]}},{"entity":"FlyBase:FBal0190540","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:5425","phenotype":{"types":[{"id":"HP:0004927","label":"Pulmonary artery dilatation"}]}},{"entity":"ClinVarVariant:36305","phenotype":{"types":[{"id":"HP:0001025","label":"Urticaria"}]}},{"entity":"ClinVarVariant:158359","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:53265","phenotype":{"types":[{"id":"HP:0011850","label":"Parotitis"}]}},{"entity":"ClinVarVariant:92564","phenotype":{"types":[{"id":"HP:0012702","label":"Tenesmus"}]}},{"entity":"ClinVarVariant:180310","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:212733","phenotype":{"types":[{"id":"HP:0003220","label":"Abnormality of chromosome stability"}]}},{"entity":"ClinVarVariant:17282","phenotype":{"types":[{"id":"HP:0004277","label":"Fractured hand bones"}]}},{"entity":"ClinVarVariant:41078","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:6935","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ZFIN:ZDB-ALT-060602-2","phenotype":{"types":[{"id":"ZP:0006118","label":"abnormal(ly) dilated enterocyte Golgi apparatus"}]}},{"entity":"ClinVarVariant:67937","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:204591","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"MGI:1856893","phenotype":{"types":[{"id":"HP:0012447","label":"Abnormal myelination"}]}},{"entity":"ClinVarVariant:101249","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:49468","phenotype":{"types":[{"id":"HP:0004755","label":"Supraventricular tachycardia"}]}},{"entity":"ClinVarVariant:157677","phenotype":{"types":[{"id":"HP:0008527","label":"Congenital sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:7132","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"MGI:3770133","phenotype":{"types":[{"id":"HP:0000618","label":"Blindness"}]}},{"entity":"ClinVarVariant:210023","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"MGI:2181380","phenotype":{"types":[{"id":"HP:0000029","label":"Testicular atrophy"}]}},{"entity":"ClinVarVariant:215572","phenotype":{"types":[{"id":"HP:0100242","label":"Sarcoma"}]}},{"entity":"ClinVarVariant:101405","phenotype":{"types":[{"id":"HP:0000963","label":"Thin skin"}]}},{"entity":"ClinVarVariant:2145","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"ClinVarVariant:53774","phenotype":{"types":[{"id":"HP:0011109","label":"Chronic sinusitis"}]}},{"entity":"ClinVarVariant:206816","phenotype":{"types":[{"id":"HP:0005484","label":"Postnatal microcephaly"}]}},{"entity":"ClinVarVariant:39442","phenotype":{"types":[{"id":"HP:0007333","label":"Hypoplasia of the frontal lobes"}]}},{"entity":"ClinVarVariant:6050","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:56814","phenotype":{"types":[{"id":"HP:0002676","label":"Cloverleaf skull"}]}},{"entity":"ClinVarVariant:3652","phenotype":{"types":[{"id":"HP:0002028","label":"Chronic diarrhea"}]}},{"entity":"MGI:3512077","phenotype":{"types":[{"id":"MP:0009419","label":"skeletal muscle fibrosis"}]}},{"entity":"ClinVarVariant:4954","phenotype":{"types":[{"id":"HP:0002315","label":"Headache"}]}},{"entity":"ClinVarVariant:101394","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:9219","phenotype":{"types":[{"id":"HP:0011157","label":"Auras"}]}},{"entity":"ClinVarVariant:3861","phenotype":{"types":[{"id":"HP:0000787","label":"Nephrolithiasis"}]}},{"entity":"ZFIN:ZDB-ALT-070309-1","phenotype":{"types":[{"id":"ZP:0010305","label":"abnormal(ly) decreased size atrioventricular canal"}]}},{"entity":"ClinVarVariant:197075","phenotype":{"types":[{"id":"HP:0000431","label":"Wide nasal bridge"}]}},{"entity":"ClinVarVariant:3612","phenotype":{"types":[{"id":"HP:0007819","label":"Presenile cataracts"}]}},{"entity":"ClinVarVariant:11340","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000912-WBRNAi00087983","phenotype":{"types":[{"id":"WBPhenotype:0001171","label":"shortened life span"}]}},{"entity":"ClinVarVariant:101155","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:53995","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:8663","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:10209","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:216067","phenotype":{"types":[{"id":"HP:0009736","label":"Tibial pseudoarthrosis"}]}},{"entity":"ClinVarVariant:211630","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00020051-WBRNAi00095700","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:18336","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:180210","phenotype":{"types":[{"id":"HP:0000974","label":"Hyperextensible skin"}]}},{"entity":"ClinVarVariant:10614","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"WormBase:WBVar00087953","phenotype":{"types":[{"id":"WBPhenotype:0001350","label":"protein phosphorylation increased"}]}},{"entity":"ClinVarVariant:189643","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:2119","phenotype":{"types":[{"id":"HP:0000174","label":"Abnormality of the palate"}]}},{"entity":"MGI:2148547","phenotype":{"types":[{"id":"MP:0006042","label":"increased apoptosis"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-110805-2-ZDB-MRPHLNO-111102-4","phenotype":{"types":[{"id":"ZP:0004922","label":"abnormal(ly) malformed neurohypophysis vasculature"}]}},{"entity":"ClinVarVariant:53748","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:208543","phenotype":{"types":[{"id":"HP:0001344","label":"Absent speech"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019481-WBRNAi00063437","phenotype":{"types":[{"id":"WBPhenotype:0000436","label":"protein subcellular localization variant"}]}},{"entity":"ClinVarVariant:53402","phenotype":{"types":[{"id":"HP:0001948","label":"Alkalosis"}]}},{"entity":"ClinVarVariant:35860","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:50235","phenotype":{"types":[{"id":"HP:0000322","label":"Short philtrum"}]}},{"entity":"ClinVarVariant:1068","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:127727","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:53640","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"MGI:1856656","phenotype":{"types":[{"id":"HP:0001254","label":"Lethargy"}]}},{"entity":"ClinVarVariant:46464","phenotype":{"types":[{"id":"HP:0000738","label":"Hallucinations"}]}},{"entity":"ClinVarVariant:54091","phenotype":{"types":[{"id":"HP:0011034","label":"Amyloidosis"}]}},{"entity":"ClinVarVariant:3221","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:159157","phenotype":{"types":[{"id":"HP:0100627","label":"Displacement of the external urethral meatus"}]}},{"entity":"ZFIN:ZDB-ALT-011017-8","phenotype":{"types":[{"id":"ZP:0013971","label":"abnormal(ly) disrupted caudal fin morphogenesis"}]}},{"entity":"ClinVarVariant:53714","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:16932","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:3157","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:216196","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:194808","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:101213","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"ClinVarVariant:46601","phenotype":{"types":[{"id":"HP:0003327","label":"Axial muscle weakness"}]}},{"entity":"ClinVarVariant:2139","phenotype":{"types":[{"id":"HP:0000089","label":"Renal hypoplasia"}]}},{"entity":"FlyBase:FBal0135890","phenotype":{"types":[{"id":"FBcv:0000411","label":"visual behavior defective"}]}},{"entity":"ClinVarVariant:126827","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:120272","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:200129","phenotype":{"types":[{"id":"HP:0001166","label":"Arachnodactyly"}]}},{"entity":"ClinVarVariant:198695","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:3773644","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"ClinVarVariant:53866","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:161355","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:13372","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004953-WBRNAi00038543","phenotype":{"types":[{"id":"WBPhenotype:0000034","label":"embryonic polarity variant"}]}},{"entity":"ClinVarVariant:56485","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:53446","phenotype":{"types":[{"id":"HP:0006538","label":"Recurrent bronchopulmonary infections"}]}},{"entity":"WormBase:WBVar00251819","phenotype":{"types":[{"id":"WBPhenotype:0000142","label":"cell stress response variant"}]}},{"entity":"ClinVarVariant:24866","phenotype":{"types":[{"id":"HP:0001636","label":"Tetralogy of Fallot"}]}},{"entity":"ClinVarVariant:4274","phenotype":{"types":[{"id":"HP:0000235","label":"Abnormality of the fontanelles or cranial sutures"}]}},{"entity":"ClinVarVariant:31695","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"FlyBase:FBal0151492","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:35875","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:36091","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"MGI:5438282","phenotype":{"types":[{"id":"MP:0005169","label":"abnormal male meiosis"}]}},{"entity":"dbSNP:rs109463474","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:21170","phenotype":{"types":[{"id":"HP:0001518","label":"Small for gestational age"}]}},{"entity":"MGI:3790794","phenotype":{"types":[{"id":"MP:0001302","label":"eyelids open at birth"}]}},{"entity":"ClinVarVariant:189730","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:182720","phenotype":{"types":[{"id":"HP:0003189","label":"Long nose"}]}},{"entity":"ClinVarVariant:53226","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:12995","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:53963","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:194320","phenotype":{"types":[{"id":"HP:0100689","label":"Decreased corneal thickness"}]}},{"entity":"ClinVarVariant:93888","phenotype":{"types":[{"id":"HP:0000311","label":"Round face"}]}},{"entity":"FlyBase:FBal0210205","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"MGI:1857326","phenotype":{"types":[{"id":"HP:0002251","label":"Aganglionic megacolon"}]}},{"entity":"ClinVarVariant:10350","phenotype":{"types":[{"id":"HP:0006380","label":"Knee flexion contracture"}]}},{"entity":"ClinVarVariant:53209","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"FlyBase:FBal0039464","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:11075","phenotype":{"types":[{"id":"HP:0100709","label":"Reduction of oligodendroglia"}]}},{"entity":"ClinVarVariant:10138","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"ClinVarVariant:39425","phenotype":{"types":[{"id":"HP:0003127","label":"Hypocalciuria"}]}},{"entity":"ClinVarVariant:35848","phenotype":{"types":[{"id":"HP:0006516","label":"Hypersensitivity pneumonitis"}]}},{"entity":"NCBIGene:791085","phenotype":{"types":[{"id":"HP:0000337","label":"Broad forehead"}]}},{"entity":"ClinVarVariant:49939","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"ClinVarVariant:30528","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"dbSNP:rs1819084","phenotype":{"types":[{"id":"HP:0002028","label":"Chronic diarrhea"}]}},{"entity":"FlyBase:FBal0219831","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:10868","phenotype":{"types":[{"id":"HP:0008572","label":"External ear malformation"}]}},{"entity":"ClinVarVariant:8267","phenotype":{"types":[{"id":"HP:0001082","label":"Cholecystitis"}]}},{"entity":"FlyBase:FBal0177466","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:11228","phenotype":{"types":[{"id":"HP:0001685","label":"Myocardial fibrosis"}]}},{"entity":"ClinVarVariant:159936","phenotype":{"types":[{"id":"HP:0040082","label":"Happy demeanor"}]}},{"entity":"ClinVarVariant:100921","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:45126","phenotype":{"types":[{"id":"HP:0002047","label":"Malignant hyperthermia"}]}},{"entity":"ClinVarVariant:12816","phenotype":{"types":[{"id":"HP:0008417","label":"Vertebral hypoplasia"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-070410-133-ZDB-MRPHLNO-130620-1","phenotype":{"types":[{"id":"ZP:0008698","label":"abnormal(ly) increased accumulation nucleate erythrocyte towards dorsal aorta"}]}},{"entity":"ClinVarVariant:127459","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"FlyBase:FBal0205974","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:163152","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:30999","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:101142","phenotype":{"types":[{"id":"HP:0000490","label":"Deeply set eye"}]}},{"entity":"FlyBase:FBal0198779","phenotype":{"types":[{"id":"FBbt:00005169PHENOTYPE","label":"Drosophila trichogen cell phenotype"}]}},{"entity":"ClinVarVariant:15644","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:210300","phenotype":{"types":[{"id":"HP:0000457","label":"Depressed nasal ridge"}]}},{"entity":"MGI:1857444","phenotype":{"types":[{"id":"GO:0045765PHENOTYPE","label":"regulation of angiogenesis phenotype"}]}},{"entity":"ClinVarVariant:49232","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:21410","phenotype":{"types":[{"id":"HP:0002069","label":"Generalized tonic-clonic seizures"}]}},{"entity":"ClinVarVariant:39727","phenotype":{"types":[{"id":"HP:0002910","label":"Elevated hepatic transaminases"}]}},{"entity":"ClinVarVariant:49105","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:53985","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:140517","phenotype":{"types":[{"id":"HP:0004540","label":"Congenital, generalized hypertrichosis"}]}},{"entity":"MGI:1933758","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:40522","phenotype":{"types":[{"id":"HP:0000276","label":"Long face"}]}},{"entity":"ClinVarVariant:4234","phenotype":{"types":[{"id":"HP:0010935","label":"Abnormality of the upper urinary tract"}]}},{"entity":"ClinVarVariant:36294","phenotype":{"types":[{"id":"HP:0000832","label":"Primary hypothyroidism"}]}},{"entity":"ClinVarVariant:65623","phenotype":{"types":[{"id":"HP:0001159","label":"Syndactyly"}]}},{"entity":"ClinVarVariant:8379","phenotype":{"types":[{"id":"HP:0003097","label":"Short femur"}]}},{"entity":"ClinVarVariant:3323","phenotype":{"types":[{"id":"HP:0008998","label":"Pectoralis hypoplasia"}]}},{"entity":"ClinVarVariant:41190","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:188880","phenotype":{"types":[{"id":"HP:0002835","label":"Aspiration"}]}},{"entity":"ClinVarVariant:36092","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:126948","phenotype":{"types":[{"id":"HP:0002435","label":"Meningocele"}]}},{"entity":"_:genid1972400","phenotype":{"types":[{"id":"ZP:0003234","label":"abnormal(ly) disrupted glomerular filtration"}]}},{"entity":"MGI:4361278","phenotype":{"types":[{"id":"HP:0003081","label":"Increased urinary potassium"}]}},{"entity":"ClinVarVariant:67539","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:53704","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"FlyBase:FBal0202908","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"MGI:1856241","phenotype":{"types":[{"id":"HP:0000134","label":"Female hypogonadism"}]}},{"entity":"WormBase:WBVar00144142","phenotype":{"types":[{"id":"WBPhenotype:0000229","label":"small"}]}},{"entity":"ClinVarVariant:210437","phenotype":{"types":[{"id":"HP:0005599","label":"Hypopigmentation of hair"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011043-WBRNAi00071240","phenotype":{"types":[{"id":"WBPhenotype:0001425","label":"receptor mediated endocytosis defective"}]}},{"entity":"MGI:3528447","phenotype":{"types":[{"id":"HP:0003138","label":"Increased blood urea nitrogen (BUN)"}]}},{"entity":"AQTL:37488","phenotype":{"types":[{"id":"AQTLTrait:1310","label":"Rabies antibody titer"}]}},{"entity":"ClinVarVariant:49163","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00020347-WBRNAi00072072","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:7178","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:45358","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"MGI:3581891","phenotype":{"types":[{"id":"MP:0004560","label":"abnormal chorionic plate morphology"}]}},{"entity":"ClinVarVariant:91610","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:30207","phenotype":{"types":[{"id":"HP:0011682","label":"Perimembranous ventricular septal defect"}]}},{"entity":"ClinVarVariant:210299","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007400-WBRNAi00080157","phenotype":{"types":[{"id":"ZP:0000676","label":"abnormal(ly) increased rate cell proliferation"}]}},{"entity":"FlyBase:FBal0258532","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:21168","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:158731","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:4889","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:3772","phenotype":{"types":[{"id":"HP:0001022","label":"Albinism"}]}},{"entity":"ClinVarVariant:49905","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:68266","phenotype":{"types":[{"id":"HP:0030273","label":"Reduced red cell adenosine deaminase activity"}]}},{"entity":"ClinVarVariant:5626","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:2446","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:9666","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:135716","phenotype":{"types":[{"id":"HP:0007649","label":"Congenital hypertrophy of retinal pigment epithelium"}]}},{"entity":"ClinVarVariant:190195","phenotype":{"types":[{"id":"HP:0002282","label":"Heterotopia"}]}},{"entity":"ClinVarVariant:42750","phenotype":{"types":[{"id":"HP:0002067","label":"Bradykinesia"}]}},{"entity":"ClinVarVariant:4335","phenotype":{"types":[{"id":"HP:0000751","label":"Personality changes"}]}},{"entity":"ClinVarVariant:204258","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:135754","phenotype":{"types":[{"id":"HP:0012539","label":"Non-Hodgkin lymphoma"}]}},{"entity":"MGI:1934195","phenotype":{"types":[{"id":"MP:0011089","label":"perinatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:35822","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"ClinVarVariant:101128","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"MGI:1856223","phenotype":{"types":[{"id":"HP:0000925","label":"Abnormality of the vertebral column"}]}},{"entity":"MGI:3848796","phenotype":{"types":[{"id":"MP:0001606","label":"impaired hematopoiesis"}]}},{"entity":"ClinVarVariant:13540","phenotype":{"types":[{"id":"HP:0001873","label":"Thrombocytopenia"}]}},{"entity":"dbSNP:rs110180463","phenotype":{"types":[{"id":"AQTLTrait:1289","label":"Milk beta-lactoglobulin protein content"}]}},{"entity":"ZFIN:ZDB-ALT-011017-8","phenotype":{"types":[{"id":"ZP:0003184","label":"abnormal(ly) aplastic dorsal longitudinal anastomotic vessel"}]}},{"entity":"MGI:2182093","phenotype":{"types":[{"id":"HP:0003323","label":"Progressive muscle weakness"}]}},{"entity":"ClinVarVariant:177941","phenotype":{"types":[{"id":"HP:0006579","label":"Prolonged neonatal jaundice"}]}},{"entity":"AQTL:5527","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:132740","phenotype":{"types":[{"id":"HP:0001578","label":"Hypercortisolism"}]}},{"entity":"ClinVarVariant:101400","phenotype":{"types":[{"id":"HP:0000790","label":"Hematuria"}]}},{"entity":"ClinVarVariant:65771","phenotype":{"types":[{"id":"HP:0002013","label":"Vomiting"}]}},{"entity":"ClinVarVariant:101174","phenotype":{"types":[{"id":"HP:0100718","label":"Uterine rupture"}]}},{"entity":"FlyBase:FBal0058990","phenotype":{"types":[{"id":"FBbt:00004508PHENOTYPE","label":"eye phenotype"}]}},{"entity":"ClinVarVariant:21502","phenotype":{"types":[{"id":"HP:0001374","label":"Congenital hip dislocation"}]}},{"entity":"ClinVarVariant:100735","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:186986","phenotype":{"types":[{"id":"HP:0002858","label":"Meningioma"}]}},{"entity":"ClinVarVariant:190262","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:56575","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"ClinVarVariant:181737","phenotype":{"types":[{"id":"HP:0009909","label":"Uplifted earlobe"}]}},{"entity":"ClinVarVariant:39095","phenotype":{"types":[{"id":"HP:0030148","label":"Heart murmur"}]}},{"entity":"ClinVarVariant:211726","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:53912","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:10184","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:56603","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:24285","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"ClinVarVariant:189633","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:25330","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:38497","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"MGI:2387580","phenotype":{"types":[{"id":"MP:0002896","label":"abnormal bone mineralization"}]}},{"entity":"ClinVarVariant:36082","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:193484","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"FlyBase:FBal0213151","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:42357","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"ClinVarVariant:6929","phenotype":{"types":[{"id":"HP:0000660","label":"Lipemia retinalis"}]}},{"entity":"ClinVarVariant:132708","phenotype":{"types":[{"id":"HP:0100242","label":"Sarcoma"}]}},{"entity":"AQTL:34784","phenotype":{"types":[{"id":"AQTLTrait:1326","label":"Milk pentadecylic acid percentage"}]}},{"entity":"ClinVarVariant:211636","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"ClinVarVariant:49721","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:10858","phenotype":{"types":[{"id":"HP:0001290","label":"Generalized hypotonia"}]}},{"entity":"ClinVarVariant:21458","phenotype":{"types":[{"id":"HP:0002511","label":"Alzheimer disease"}]}},{"entity":"MGI:4459519","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:12985","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:49995","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"ClinVarVariant:99928","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:67700","phenotype":{"types":[{"id":"HP:0006682","label":"Ventricular extrasystoles"}]}},{"entity":"ClinVarVariant:17093","phenotype":{"types":[{"id":"HP:0100615","label":"Ovarian neoplasm"}]}},{"entity":"MGI:3611770","phenotype":{"types":[{"id":"MP:0004043","label":"abnormal pH regulation"}]}},{"entity":"ClinVarVariant:10604","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"ClinVarVariant:159928","phenotype":{"types":[{"id":"HP:0001939","label":"Abnormality of metabolism/homeostasis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00009365-WBRNAi00002028","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:135765","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:67966","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:38752","phenotype":{"types":[{"id":"HP:0010741","label":"Edema of the lower limbs"}]}},{"entity":"ClinVarVariant:190261","phenotype":{"types":[{"id":"HP:0100699","label":"Scarring"}]}},{"entity":"ClinVarVariant:215580","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:15443","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"ClinVarVariant:143754","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ClinVarVariant:53204","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:39769","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:204046","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:53564","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"MGI:2152962","phenotype":{"types":[{"id":"MP:0003984","label":"embryonic growth retardation"}]}},{"entity":"ClinVarVariant:4800","phenotype":{"types":[{"id":"HP:0002754","label":"Osteomyelitis"}]}},{"entity":"ClinVarVariant:68716","phenotype":{"types":[{"id":"HP:0007109","label":"Periventricular cysts"}]}},{"entity":"ClinVarVariant:126966","phenotype":{"types":[{"id":"HP:0009713","label":"Spinal hemangioblastoma"}]}},{"entity":"ClinVarVariant:158339","phenotype":{"types":[{"id":"HP:0000343","label":"Long philtrum"}]}},{"entity":"ClinVarVariant:18035","phenotype":{"types":[{"id":"HP:0004850","label":"Recurrent deep vein thrombosis"}]}},{"entity":"ClinVarVariant:94804","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:188862","phenotype":{"types":[{"id":"HP:0002487","label":"Hyperkinesis"}]}},{"entity":"ClinVarVariant:12799","phenotype":{"types":[{"id":"HP:0000133","label":"Gonadal dysgenesis"}]}},{"entity":"ClinVarVariant:10163","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"ClinVarVariant:30294","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:159097","phenotype":{"types":[{"id":"HP:0005815","label":"Supernumerary ribs"}]}},{"entity":"ClinVarVariant:41245","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"ClinVarVariant:3196","phenotype":{"types":[{"id":"HP:0003411","label":"Proximal femoral metaphyseal irregularity"}]}},{"entity":"ClinVarVariant:13567","phenotype":{"types":[{"id":"HP:0000132","label":"Menorrhagia"}]}},{"entity":"ClinVarVariant:41132","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00077526-WBRNAi00070047","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:3813","phenotype":{"types":[{"id":"HP:0004332","label":"Abnormality of lymphocytes"}]}},{"entity":"ClinVarVariant:53734","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"_:genid1976152","phenotype":{"types":[{"id":"ZP:0001609","label":"abnormal(ly) morphology head"}]}},{"entity":"ClinVarVariant:68264","phenotype":{"types":[{"id":"HP:0002644","label":"Abnormality of pelvic girdle bone morphology"}]}},{"entity":"ClinVarVariant:8542","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:53935","phenotype":{"types":[{"id":"HP:0100512","label":"Vitamin D deficiency"}]}},{"entity":"ClinVarVariant:534","phenotype":{"types":[{"id":"HP:0000597","label":"Ophthalmoparesis"}]}},{"entity":"ClinVarVariant:9177","phenotype":{"types":[{"id":"HP:0000384","label":"Preauricular skin tag"}]}},{"entity":"ClinVarVariant:3684","phenotype":{"types":[{"id":"HP:0001114","label":"Xanthelasma"}]}},{"entity":"ClinVarVariant:94605","phenotype":{"types":[{"id":"HP:0002948","label":"Vertebral fusion"}]}},{"entity":"FlyBase:FBal0203313","phenotype":{"types":[{"id":"FBcv:0000352","label":"partially lethal - majority die"}]}},{"entity":"ClinVarVariant:211625","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"MGI:1861958","phenotype":{"types":[{"id":"MP:0009684","label":"abnormal spinal cord lateral motor column morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001746-WBRNAi00084506","phenotype":{"types":[{"id":"WBPhenotype:0001235","label":"cell division polarity variant"}]}},{"entity":"ClinVarVariant:2074","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:189159","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:1033","phenotype":{"types":[{"id":"HP:0003103","label":"Abnormal cortical bone morphology"}]}},{"entity":"ClinVarVariant:6834","phenotype":{"types":[{"id":"HP:0003422","label":"Vertebral segmentation defect"}]}},{"entity":"ClinVarVariant:2076","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"FlyBase:FBal0260715","phenotype":{"types":[{"id":"FBbt:00100529PHENOTYPE","label":"Drosophila embryonic/larval carpet glial cell phenotype"}]}},{"entity":"ClinVarVariant:7994","phenotype":{"types":[{"id":"HP:0009777","label":"Absent thumb"}]}},{"entity":"dbSNP:rs41649184","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:158353","phenotype":{"types":[{"id":"HP:0000742","label":"Self-mutilation"}]}},{"entity":"ClinVarVariant:21535","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:49711","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:35850","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"MGI:3847254","phenotype":{"types":[{"id":"MP:0008237","label":"abnormal ventral coat pigmentation"}]}},{"entity":"ClinVarVariant:36970","phenotype":{"types":[{"id":"HP:0007925","label":"Lacrimal duct aplasia"}]}},{"entity":"ClinVarVariant:13455","phenotype":{"types":[{"id":"HP:0001269","label":"Hemiparesis"}]}},{"entity":"ClinVarVariant:24427","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"ClinVarVariant:24538","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:6051","phenotype":{"types":[{"id":"HP:0100864","label":"Short femoral neck"}]}},{"entity":"ClinVarVariant:7172","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:197156","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:10756","phenotype":{"types":[{"id":"HP:0009830","label":"Peripheral neuropathy"}]}},{"entity":"ClinVarVariant:24299","phenotype":{"types":[{"id":"HP:0000613","label":"Photophobia"}]}},{"entity":"ClinVarVariant:24458","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:93896","phenotype":{"types":[{"id":"HP:0003236","label":"Elevated serum creatine phosphokinase"}]}},{"entity":"ClinVarVariant:159941","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:12403","phenotype":{"types":[{"id":"HP:0009727","label":"Achromatic retinal patches"}]}},{"entity":"ClinVarVariant:10713","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"dbSNP:rs12294076","phenotype":{"types":[{"id":"HP:0002102","label":"Pleuritis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011944-WBRNAi00072116","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"MGI:5615712","phenotype":{"types":[{"id":"MP:0020001","label":"decreased response to antigen"}]}},{"entity":"ClinVarVariant:67927","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:24498","phenotype":{"types":[{"id":"HP:0000517","label":"Abnormality of the lens"}]}},{"entity":"ClinVarVariant:31879","phenotype":{"types":[{"id":"HP:0001712","label":"Left ventricular hypertrophy"}]}},{"entity":"ClinVarVariant:12880","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:49701","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:54093","phenotype":{"types":[{"id":"HP:0004401","label":"Meconium ileus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00013532-WBRNAi00058395","phenotype":{"types":[{"id":"WBPhenotype:0000056","label":"late larval arrest"}]}},{"entity":"ZFIN:ZDB-ALT-150528-4","phenotype":{"types":[{"id":"ZP:0012747","label":"abnormal(ly) process quality cranial neural crest neural crest cell migration"}]}},{"entity":"ClinVarVariant:197759","phenotype":{"types":[{"id":"HP:0005107","label":"Abnormality of the sacrum"}]}},{"entity":"ClinVarVariant:8711","phenotype":{"types":[{"id":"HP:0001895","label":"Normochromic anemia"}]}},{"entity":"ClinVarVariant:196933","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:31592","phenotype":{"types":[{"id":"HP:0003034","label":"Diaphyseal sclerosis"}]}},{"entity":"ClinVarVariant:6221","phenotype":{"types":[{"id":"HP:0100335","label":"Non-midline cleft lip"}]}},{"entity":"ClinVarVariant:210043","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"MGI:3809665","phenotype":{"types":[{"id":"MP:0004946","label":"abnormal regulatory T cell physiology"}]}},{"entity":"ClinVarVariant:1569","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"_:genid1976482","phenotype":{"types":[{"id":"ZP:0010599","label":"abnormal(ly) position ceratohyal cartilage"}]}},{"entity":"ClinVarVariant:210790","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"MGI:3583779","phenotype":{"types":[{"id":"MP:0012113","label":"decreased inner cell mass proliferation"}]}},{"entity":"ClinVarVariant:56697","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"NCBIGene:1165","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:54033","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:210476","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"ClinVarVariant:204036","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:2236","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"MGI:1857189","phenotype":{"types":[{"id":"MP:0008211","label":"decreased mature B cell number"}]}},{"entity":"ClinVarVariant:35895","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:10110","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"ClinVarVariant:189153","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:36511","phenotype":{"types":[{"id":"HP:0002633","label":"Vasculitis"}]}},{"entity":"ClinVarVariant:135748","phenotype":{"types":[{"id":"HP:0008348","label":"Immunoglobulin IgG2 deficiency"}]}},{"entity":"MGI:3815539","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:5419","phenotype":{"types":[{"id":"HP:0002150","label":"Hypercalciuria"}]}},{"entity":"MGI:2668901","phenotype":{"types":[{"id":"MP:0002655","label":"abnormal keratinocyte morphology"}]}},{"entity":"ClinVarVariant:156349","phenotype":{"types":[{"id":"HP:0000227","label":"Tongue telangiectasia"}]}},{"entity":"ClinVarVariant:159039","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:29639","phenotype":{"types":[{"id":"HP:0000689","label":"Dental malocclusion"}]}},{"entity":"ClinVarVariant:297","phenotype":{"types":[{"id":"HP:0001873","label":"Thrombocytopenia"}]}},{"entity":"dbSNP:rs132692798","phenotype":{"types":[{"id":"AQTLTrait:1327","label":"Milk odd-chain fatty acid percentage"}]}},{"entity":"ClinVarVariant:216944","phenotype":{"types":[{"id":"HP:0002170","label":"Intracranial hemorrhage"}]}},{"entity":"ClinVarVariant:181713","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:53915","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"dbSNP:rs42436295","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:12661","phenotype":{"types":[{"id":"HP:0008981","label":"Calf muscle hypertrophy"}]}},{"entity":"ClinVarVariant:11040","phenotype":{"types":[{"id":"HP:0007411","label":"Hypoplastic-absent sebaceous glands"}]}},{"entity":"ClinVarVariant:143171","phenotype":{"types":[{"id":"HP:0001123","label":"Visual field defect"}]}},{"entity":"ClinVarVariant:53990","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"ClinVarVariant:24866","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"FlyBase:FBal0296742","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007029-WBRNAi00088606","phenotype":{"types":[{"id":"WBPhenotype:0002057","label":"Bacillus thuringiensis toxin hypersensitive"}]}},{"entity":"ClinVarVariant:161357","phenotype":{"types":[{"id":"HP:0000303","label":"Mandibular prognathia"}]}},{"entity":"FlyBase:FBal0204265","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:65606","phenotype":{"types":[{"id":"HP:0001507","label":"Growth abnormality"}]}},{"entity":"ClinVarVariant:53961","phenotype":{"types":[{"id":"HP:0011947","label":"Respiratory tract infection"}]}},{"entity":"ClinVarVariant:135882","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:38742","phenotype":{"types":[{"id":"HP:0000519","label":"Congenital cataract"}]}},{"entity":"ClinVarVariant:41146","phenotype":{"types":[{"id":"HP:0100267","label":"Lip pit"}]}},{"entity":"ClinVarVariant:53803","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:189663","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:24409","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"MGI:2449695","phenotype":{"types":[{"id":"MP:0002563","label":"shortened circadian period"}]}},{"entity":"ClinVarVariant:24611","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:53964","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:189931","phenotype":{"types":[{"id":"HP:0005484","label":"Postnatal microcephaly"}]}},{"entity":"ClinVarVariant:30665","phenotype":{"types":[{"id":"HP:0000230","label":"Gingivitis"}]}},{"entity":"ClinVarVariant:40257","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"MGI:1856209","phenotype":{"types":[{"id":"GO:0021953PHENOTYPE","label":"central nervous system neuron differentiation phenotype"}]}},{"entity":"ClinVarVariant:24512","phenotype":{"types":[{"id":"HP:0000099","label":"Glomerulonephritis"}]}},{"entity":"ClinVarVariant:44811","phenotype":{"types":[{"id":"HP:0009891","label":"Underdeveloped supraorbital ridges"}]}},{"entity":"ClinVarVariant:8870","phenotype":{"types":[{"id":"HP:0002823","label":"Abnormality of the femur"}]}},{"entity":"ClinVarVariant:10156","phenotype":{"types":[{"id":"HP:0005268","label":"Spontaneous abortion"}]}},{"entity":"ClinVarVariant:210476","phenotype":{"types":[{"id":"HP:0003819","label":"Death in childhood"}]}},{"entity":"MGI:4818801","phenotype":{"types":[{"id":"HP:0001899","label":"Increased hematocrit"}]}},{"entity":"ClinVarVariant:10733","phenotype":{"types":[{"id":"HP:0009763","label":"Limb pain"}]}},{"entity":"FlyBase:FBal0102482","phenotype":{"types":[{"id":"FBcv:0000377","label":"female fertile"}]}},{"entity":"AQTL:54943","phenotype":{"types":[{"id":"AQTLTrait:1004","label":"Somatic cell count"}]}},{"entity":"ClinVarVariant:56625","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:6574","phenotype":{"types":[{"id":"HP:0010783","label":"Erythema"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004813-WBRNAi00075001","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:13823","phenotype":{"types":[{"id":"HP:0002164","label":"Nail dysplasia"}]}},{"entity":"ClinVarVariant:195148","phenotype":{"types":[{"id":"HP:0004327","label":"Abnormality of the vitreous humor"}]}},{"entity":"ClinVarVariant:40502","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:135886","phenotype":{"types":[{"id":"HP:0009733","label":"Glioma"}]}},{"entity":"ClinVarVariant:53932","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:49565","phenotype":{"types":[{"id":"HP:0009716","label":"Subependymal nodules"}]}},{"entity":"ClinVarVariant:13658","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"ClinVarVariant:21160","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"MGI:1857872","phenotype":{"types":[{"id":"MP:0008813","label":"decreased common myeloid progenitor cell number"}]}},{"entity":"ClinVarVariant:183748","phenotype":{"types":[{"id":"HP:0100568","label":"Neoplasm of the endocrine system"}]}},{"entity":"ClinVarVariant:50050","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"ClinVarVariant:56475","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:17974","phenotype":{"types":[{"id":"HP:0002613","label":"Biliary cirrhosis"}]}},{"entity":"MGI:1860866","phenotype":{"types":[{"id":"GO:0051209PHENOTYPE","label":"release of sequestered calcium ion into cytosol phenotype"}]}},{"entity":"MGI:3044898","phenotype":{"types":[{"id":"MP:0013716","label":"hypolactation"}]}},{"entity":"ClinVarVariant:216231","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:188863","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"ClinVarVariant:162395","phenotype":{"types":[{"id":"HP:0010819","label":"Atonic seizures"}]}},{"entity":"MGI:3027823","phenotype":{"types":[{"id":"MP:0001929","label":"abnormal gametogenesis"}]}},{"entity":"ClinVarVariant:1075","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"WormBase:WBVar00094804","phenotype":{"types":[{"id":"WBPhenotype:0001059","label":"magnesium chemotaxis defective"}]}},{"entity":"ClinVarVariant:13001","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:4849547","phenotype":{"types":[{"id":"HP:0002213","label":"Fine hair"}]}},{"entity":"ClinVarVariant:143564","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"ClinVarVariant:209010","phenotype":{"types":[{"id":"HP:0100660","label":"Dyskinesia"}]}},{"entity":"ClinVarVariant:210389","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"MGI:3848347","phenotype":{"types":[{"id":"GO:0008584PHENOTYPE","label":"male gonad development phenotype"}]}},{"entity":"ClinVarVariant:24268","phenotype":{"types":[{"id":"HP:0100273","label":"Neoplasm of the colon"}]}},{"entity":"ClinVarVariant:143744","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ClinVarVariant:68490","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001337-WBRNAi00096891","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:132795","phenotype":{"types":[{"id":"HP:0001874","label":"Abnormality of neutrophils"}]}},{"entity":"ClinVarVariant:158349","phenotype":{"types":[{"id":"HP:0009765","label":"Low hanging columella"}]}},{"entity":"ClinVarVariant:65343","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:11642","phenotype":{"types":[{"id":"HP:0006887","label":"Intellectual disability, progressive"}]}},{"entity":"ClinVarVariant:161287","phenotype":{"types":[{"id":"HP:0001084","label":"Corneal arcus"}]}},{"entity":"ClinVarVariant:29790","phenotype":{"types":[{"id":"HP:0003690","label":"Limb muscle weakness"}]}},{"entity":"MGI:2682016","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"MGI:1932294","phenotype":{"types":[{"id":"HP:0012447","label":"Abnormal myelination"}]}},{"entity":"ClinVarVariant:6794","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:24762","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:21252","phenotype":{"types":[{"id":"HP:0000202","label":"Oral cleft"}]}},{"entity":"ClinVarVariant:53933","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:49411","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"MGI:2136432","phenotype":{"types":[{"id":"MP:0001284","label":"absent vibrissae"}]}},{"entity":"dbSNP:rs109445675","phenotype":{"types":[{"id":"AQTLTrait:1130","label":"Udder cleft"}]}},{"entity":"ClinVarVariant:10912","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"FlyBase:FBal0197136","phenotype":{"types":[{"id":"FBcv:0000397","label":"learning defective"}]}},{"entity":"ClinVarVariant:42756","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:36501","phenotype":{"types":[{"id":"HP:0002633","label":"Vasculitis"}]}},{"entity":"ClinVarVariant:101125","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"ClinVarVariant:6834","phenotype":{"types":[{"id":"HP:0000337","label":"Broad forehead"}]}},{"entity":"FlyBase:FBal0206542","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:9162","phenotype":{"types":[{"id":"HP:0011106","label":"Hypovolemia"}]}},{"entity":"ClinVarVariant:692","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:204026","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:1775","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:164883","phenotype":{"types":[{"id":"HP:0000540","label":"Hypermetropia"}]}},{"entity":"ClinVarVariant:10249","phenotype":{"types":[{"id":"HP:0100845","label":"Anaphylactic shock"}]}},{"entity":"ClinVarVariant:53724","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:24448","phenotype":{"types":[{"id":"HP:0200020","label":"Corneal erosion"}]}},{"entity":"ClinVarVariant:43146","phenotype":{"types":[{"id":"HP:0008555","label":"Absent vestibular function"}]}},{"entity":"ClinVarVariant:54021","phenotype":{"types":[{"id":"HP:0005948","label":"Cystic lung disease"}]}},{"entity":"ClinVarVariant:202199","phenotype":{"types":[{"id":"HP:0005257","label":"Thoracic hypoplasia"}]}},{"entity":"ClinVarVariant:24339","phenotype":{"types":[{"id":"HP:0100539","label":"Periorbital edema"}]}},{"entity":"ClinVarVariant:136155","phenotype":{"types":[{"id":"HP:0000582","label":"Upslanted palpebral fissure"}]}},{"entity":"ClinVarVariant:91600","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:50098","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"ZFIN:ZDB-ALT-071108-4","phenotype":{"types":[{"id":"ZP:0005125","label":"abnormal(ly) decreased size swim bladder"}]}},{"entity":"ClinVarVariant:1371","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"ClinVarVariant:56662","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:6540","phenotype":{"types":[{"id":"HP:0200042","label":"Skin ulcer"}]}},{"entity":"ClinVarVariant:210388","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"ClinVarVariant:40726","phenotype":{"types":[{"id":"HP:0000027","label":"Azoospermia"}]}},{"entity":"ClinVarVariant:24996","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:100739","phenotype":{"types":[{"id":"HP:0000484","label":"Hyperopic astigmatism"}]}},{"entity":"ClinVarVariant:189599","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"ClinVarVariant:158080","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:678","phenotype":{"types":[{"id":"HP:0005543","label":"Reduced protein C activity"}]}},{"entity":"ClinVarVariant:159036","phenotype":{"types":[{"id":"HP:0200054","label":"Monodactyly (feet)"}]}},{"entity":"ClinVarVariant:188984","phenotype":{"types":[{"id":"HP:0006887","label":"Intellectual disability, progressive"}]}},{"entity":"ClinVarVariant:6593","phenotype":{"types":[{"id":"HP:0003155","label":"Elevated alkaline phosphatase"}]}},{"entity":"ClinVarVariant:133628","phenotype":{"types":[{"id":"HP:0005425","label":"Recurrent sinopulmonary infections"}]}},{"entity":"ClinVarVariant:217297","phenotype":{"types":[{"id":"HP:0001144","label":"Orbital cyst"}]}},{"entity":"ClinVarVariant:40869","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004873-WBRNAi00037161","phenotype":{"types":[{"id":"WBPhenotype:0000025","label":"blistered"}]}},{"entity":"ClinVarVariant:41095","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:189125","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:6969","phenotype":{"types":[{"id":"HP:0003148","label":"Elevated serum acid phosphatase"}]}},{"entity":"ClinVarVariant:194120","phenotype":{"types":[{"id":"HP:0000657","label":"Oculomotor apraxia"}]}},{"entity":"ClinVarVariant:56314","phenotype":{"types":[{"id":"HP:0001562","label":"Oligohydramnios"}]}},{"entity":"MGI:2679338","phenotype":{"types":[{"id":"MP:0001473","label":"reduced long term potentiation"}]}},{"entity":"ClinVarVariant:56354","phenotype":{"types":[{"id":"HP:0012156","label":"Hemophagocytosis"}]}},{"entity":"ClinVarVariant:7152","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:210259","phenotype":{"types":[{"id":"HP:0002592","label":"Gastric ulcer"}]}},{"entity":"FlyBase:FBal0057699","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:10649","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:101259","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:157613","phenotype":{"types":[{"id":"HP:0000510","label":"Rod-cone dystrophy"}]}},{"entity":"ClinVarVariant:189653","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:210033","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:13343","phenotype":{"types":[{"id":"HP:0008357","label":"Reduced factor XIII activity"}]}},{"entity":"ClinVarVariant:40525","phenotype":{"types":[{"id":"HP:0030084","label":"Clinodactyly"}]}},{"entity":"ClinVarVariant:45358","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"ClinVarVariant:190395","phenotype":{"types":[{"id":"HP:0011100","label":"Intestinal atresia"}]}},{"entity":"MGI:2384087","phenotype":{"types":[{"id":"HP:0040171","label":"Decreased serum testosterone level"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008476-WBRNAi00024985","phenotype":{"types":[{"id":"WBPhenotype:0000054","label":"larval lethal"}]}},{"entity":"AQTL:30584","phenotype":{"types":[{"id":"AQTLTrait:1559","label":"Cell-mediated immune response"}]}},{"entity":"ClinVarVariant:204107","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:127339","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00018156-WBRNAi00087047","phenotype":{"types":[{"id":"WBPhenotype:0000038","label":"exploded through vulva"}]}},{"entity":"FlyBase:FBal0117671","phenotype":{"types":[{"id":"FBcv:0000358","label":"small body"}]}},{"entity":"MGI:1926498","phenotype":{"types":[{"id":"HP:0000962","label":"Hyperkeratosis"}]}},{"entity":"ClinVarVariant:52348","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"MGI:5297555","phenotype":{"types":[{"id":"MP:0001258","label":"decreased body length"}]}},{"entity":"AQTL:14959","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002226-WBRNAi00074011","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:17112","phenotype":{"types":[{"id":"HP:0007759","label":"Opacification of the corneal stroma"}]}},{"entity":"ClinVarVariant:7624","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:4566","phenotype":{"types":[{"id":"HP:0003487","label":"Babinski sign"}]}},{"entity":"ClinVarVariant:41167","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:132684","phenotype":{"types":[{"id":"HP:0000982","label":"Palmoplantar keratoderma"}]}},{"entity":"MGI:2183411","phenotype":{"types":[{"id":"HP:0011805","label":"Abnormality of muscle morphology"}]}},{"entity":"FlyBase:FBal0210631","phenotype":{"types":[{"id":"FBbt:00005179PHENOTYPE","label":"Drosophila macrochaeta phenotype"}]}},{"entity":"ClinVarVariant:11742","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:66001","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:97544","phenotype":{"types":[{"id":"HP:0000999","label":"Pyoderma"}]}},{"entity":"ClinVarVariant:3364","phenotype":{"types":[{"id":"HP:0001012","label":"Multiple lipomas"}]}},{"entity":"MGI:1857711","phenotype":{"types":[{"id":"GO:0007281PHENOTYPE","label":"germ cell development phenotype"}]}},{"entity":"ClinVarVariant:97000","phenotype":{"types":[{"id":"HP:0000012","label":"Urinary urgency"}]}},{"entity":"MGI:3762119","phenotype":{"types":[{"id":"HP:0011018","label":"Abnormality of the cell cycle"}]}},{"entity":"ClinVarVariant:682","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:159807","phenotype":{"types":[{"id":"HP:0000405","label":"Conductive hearing impairment"}]}},{"entity":"ClinVarVariant:16635","phenotype":{"types":[{"id":"HP:0002027","label":"Abdominal pain"}]}},{"entity":"ClinVarVariant:49482","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"ClinVarVariant:68721","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"dbSNP:rs41668337","phenotype":{"types":[{"id":"AQTLTrait:1115","label":"Chest width"}]}},{"entity":"FlyBase:FBal0239202","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:196726","phenotype":{"types":[{"id":"HP:0001030","label":"Fragile skin"}]}},{"entity":"ClinVarVariant:45344","phenotype":{"types":[{"id":"HP:0004808","label":"Acute myeloid leukemia"}]}},{"entity":"AQTL:3668","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:189693","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:53715","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"dbSNP:rs109089392","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"ClinVarVariant:49560","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:54195","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:204076","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:67917","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:5823","phenotype":{"types":[{"id":"HP:0008472","label":"Prominent protruding coccyx"}]}},{"entity":"ClinVarVariant:2656","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:17112","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"dbSNP:rs3800569","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:40522","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"MGI:1857826","phenotype":{"types":[{"id":"MP:0004453","label":"abnormal pterygoid bone morphology"}]}},{"entity":"ClinVarVariant:66473","phenotype":{"types":[{"id":"HP:0007360","label":"Aplasia/Hypoplasia of the cerebellum"}]}},{"entity":"ClinVarVariant:43580","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"MGI:2656537","phenotype":{"types":[{"id":"HP:0001322","label":"Brain very small"}]}},{"entity":"ClinVarVariant:49781","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:31562","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:39479","phenotype":{"types":[{"id":"HP:0000944","label":"Abnormality of the metaphyses"}]}},{"entity":"ClinVarVariant:188339","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:35840","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:39824","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:211909","phenotype":{"types":[{"id":"HP:0007772","label":"Impaired smooth pursuit"}]}},{"entity":"ClinVarVariant:1078","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:127707","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008053-WBRNAi00093392","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"MGI:3772332","phenotype":{"types":[{"id":"MP:0008209","label":"decreased pre-B cell number"}]}},{"entity":"ClinVarVariant:65877","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:31054","phenotype":{"types":[{"id":"HP:0000625","label":"Cleft eyelid"}]}},{"entity":"ClinVarVariant:18337","phenotype":{"types":[{"id":"HP:0009773","label":"Symphalangism affecting the phalanges of the hand"}]}},{"entity":"ClinVarVariant:53397","phenotype":{"types":[{"id":"HP:0005214","label":"Intestinal obstruction"}]}},{"entity":"WormBase:WBVar00089700","phenotype":{"types":[{"id":"WBPhenotype:0000216","label":"cell fate specification variant"}]}},{"entity":"MGI:5691529","phenotype":{"types":[{"id":"HP:0003196","label":"Short nose"}]}},{"entity":"FlyBase:FBal0117901","phenotype":{"types":[{"id":"FBbt:00001055PHENOTYPE","label":"presumptive embryonic/larval nervous system phenotype"}]}},{"entity":"ClinVarVariant:53754","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"MGI:4881474","phenotype":{"types":[{"id":"MP:0002945","label":"abnormal inhibitory postsynaptic currents"}]}},{"entity":"ClinVarVariant:42177","phenotype":{"types":[{"id":"HP:0002110","label":"Bronchiectasis"}]}},{"entity":"ClinVarVariant:101218","phenotype":{"types":[{"id":"HP:0100585","label":"Telangiectasia of the skin"}]}},{"entity":"ClinVarVariant:209131","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:7393","phenotype":{"types":[{"id":"HP:0000135","label":"Hypogonadism"}]}},{"entity":"ClinVarVariant:95639","phenotype":{"types":[{"id":"HP:0009909","label":"Uplifted earlobe"}]}},{"entity":"ClinVarVariant:49771","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:101223","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"ClinVarVariant:10053","phenotype":{"types":[{"id":"HP:0007325","label":"Generalized dystonia"}]}},{"entity":"ClinVarVariant:56402","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:3862","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"_:genid1975835","phenotype":{"types":[{"id":"ZP:0001663","label":"abnormal(ly) increased branchiness motor neuron axon"}]}},{"entity":"ClinVarVariant:24237","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"FlyBase:FBal0268981","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:166813","phenotype":{"types":[{"id":"HP:0010780","label":"Hyperacusis"}]}},{"entity":"ClinVarVariant:181733","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"MGI:3691651","phenotype":{"types":[{"id":"HP:0003330","label":"Abnormal bone structure"}]}},{"entity":"FlyBase:FBal0200319","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:215765","phenotype":{"types":[{"id":"HP:0005562","label":"Multiple renal cysts"}]}},{"entity":"FlyBase:FBal0190677","phenotype":{"types":[{"id":"FBbt:00005378PHENOTYPE","label":"wing margin phenotype"}]}},{"entity":"ClinVarVariant:53650","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:13329","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:54009","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"MGI:5297120","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:7184","phenotype":{"types":[{"id":"HP:0100027","label":"Recurrent pancreatitis"}]}},{"entity":"ClinVarVariant:49286","phenotype":{"types":[{"id":"HP:0009717","label":"Cortical tubers"}]}},{"entity":"ClinVarVariant:101289","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:11707","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:99920","phenotype":{"types":[{"id":"HP:0000289","label":"Broad philtrum"}]}},{"entity":"ClinVarVariant:17229","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1756","phenotype":{"types":[{"id":"ZP:0000212","label":"abnormal(ly) viability whole organism"}]}},{"entity":"ClinVarVariant:156620","phenotype":{"types":[{"id":"HP:0100021","label":"Cerebral palsy"}]}},{"entity":"ClinVarVariant:54067","phenotype":{"types":[{"id":"HP:0011109","label":"Chronic sinusitis"}]}},{"entity":"ClinVarVariant:53736","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"MGI:2179460","phenotype":{"types":[{"id":"MP:0009678","label":"abnormal spinal cord lateral column morphology"}]}},{"entity":"ClinVarVariant:188794","phenotype":{"types":[{"id":"HP:0002015","label":"Dysphagia"}]}},{"entity":"ClinVarVariant:12000","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00020263-WBRNAi00026196","phenotype":{"types":[{"id":"WBPhenotype:0000697","label":"protruding vulva"}]}},{"entity":"ClinVarVariant:68596","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:210780","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:41258","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"ClinVarVariant:4627","phenotype":{"types":[{"id":"HP:0003390","label":"Sensory axonal neuropathy"}]}},{"entity":"ClinVarVariant:21156","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ZFIN:ZDB-ALT-080325-1","phenotype":{"types":[{"id":"ZP:0015389","label":"abnormal(ly) non-functional sperm mitochondrion"}]}},{"entity":"ClinVarVariant:159236","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:30170","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:12672","phenotype":{"types":[{"id":"HP:0000963","label":"Thin skin"}]}},{"entity":"ClinVarVariant:9001","phenotype":{"types":[{"id":"HP:0010971","label":"Absence of Lutheran antigen on erythrocytes"}]}},{"entity":"ClinVarVariant:210789","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"MGI:3576671","phenotype":{"types":[{"id":"HP:0000021","label":"Megacystis"}]}},{"entity":"ClinVarVariant:10758","phenotype":{"types":[{"id":"HP:0000763","label":"Sensory neuropathy"}]}},{"entity":"ClinVarVariant:10063","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:53952","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050913-84-ZDB-MRPHLNO-070713-2","phenotype":{"types":[{"id":"ZP:0007928","label":"abnormal(ly) edematous heart sarcolemma"}]}},{"entity":"ClinVarVariant:66925","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"MGI:2150346","phenotype":{"types":[{"id":"MP:0009039","label":"absent inferior colliculus"}]}},{"entity":"ClinVarVariant:12607","phenotype":{"types":[{"id":"HP:0000474","label":"Thickened nuchal skin fold"}]}},{"entity":"FlyBase:FBal0230895","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:36132","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:180361","phenotype":{"types":[{"id":"HP:0011645","label":"Sinus of Valsalva aneurysm"}]}},{"entity":"ClinVarVariant:11010","phenotype":{"types":[{"id":"HP:0002021","label":"Pyloric stenosis"}]}},{"entity":"ClinVarVariant:9378","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:65730","phenotype":{"types":[{"id":"HP:0000722","label":"Obsessive-compulsive behavior"}]}},{"entity":"MGI:3036704","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"ClinVarVariant:14087","phenotype":{"types":[{"id":"HP:0001712","label":"Left ventricular hypertrophy"}]}},{"entity":"FlyBase:FBal0204597","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:16911","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:53117","phenotype":{"types":[{"id":"HP:0006696","label":"Polymorphic and polytopic ventricular extrasystoles"}]}},{"entity":"ClinVarVariant:56312","phenotype":{"types":[{"id":"HP:0002323","label":"Anencephaly"}]}},{"entity":"ClinVarVariant:24391","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"ClinVarVariant:94001","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:10289","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:6207","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:127348","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"FlyBase:FBal0202458","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:180411","phenotype":{"types":[{"id":"HP:0100749","label":"Chest pain"}]}},{"entity":"ClinVarVariant:200598","phenotype":{"types":[{"id":"HP:0006696","label":"Polymorphic and polytopic ventricular extrasystoles"}]}},{"entity":"ClinVarVariant:53214","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:11819","phenotype":{"types":[{"id":"HP:0000721","label":"Lack of spontaneous play"}]}},{"entity":"AQTL:51680","phenotype":{"types":[{"id":"AQTLTrait:1120","label":"Thurl width"}]}},{"entity":"FlyBase:FBal0124348","phenotype":{"types":[{"id":"FBcv:0000432","label":"mitotic cell cycle defective"}]}},{"entity":"ClinVarVariant:5086","phenotype":{"types":[{"id":"HP:0000666","label":"Horizontal nystagmus"}]}},{"entity":"dbSNP:rs16879552","phenotype":{"types":[{"id":"HP:0005249","label":"Functional intestinal obstruction"}]}},{"entity":"ClinVarVariant:101196","phenotype":{"types":[{"id":"HP:0000387","label":"Absent earlobe"}]}},{"entity":"MGI:4318693","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006366-WBRNAi00086348","phenotype":{"types":[{"id":"WBPhenotype:0000154","label":"reduced brood size"}]}},{"entity":"WormBase:WBVar00143937","phenotype":{"types":[{"id":"WBPhenotype:0000502","label":"right handed roller"}]}},{"entity":"ClinVarVariant:93356","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:55952","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:155982","phenotype":{"types":[{"id":"HP:0200085","label":"Limb tremor"}]}},{"entity":"ClinVarVariant:204102","phenotype":{"types":[{"id":"HP:0000121","label":"Nephrocalcinosis"}]}},{"entity":"MGI:3837125","phenotype":{"types":[{"id":"MP:0005154","label":"increased B cell proliferation"}]}},{"entity":"ClinVarVariant:36122","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:189043","phenotype":{"types":[{"id":"HP:0002967","label":"Cubitus valgus"}]}},{"entity":"ClinVarVariant:167563","phenotype":{"types":[{"id":"HP:0007018","label":"Attention deficit hyperactivity disorder"}]}},{"entity":"ClinVarVariant:216025","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:5973","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"MGI:2156086","phenotype":{"types":[{"id":"MP:0003645","label":"increased pancreatic beta cell number"}]}},{"entity":"ClinVarVariant:25340","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:216143","phenotype":{"types":[{"id":"HP:0001350","label":"Slurred speech"}]}},{"entity":"AQTL:49968","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"MGI:4440831","phenotype":{"types":[{"id":"MP:0011095","label":"embryonic lethality between implantation and placentation, complete penetrance"}]}},{"entity":"WormBase:WBVar00146423","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:7460","phenotype":{"types":[{"id":"HP:0000069","label":"Abnormality of the ureter"}]}},{"entity":"ClinVarVariant:157618","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"ClinVarVariant:10198","phenotype":{"types":[{"id":"HP:0100310","label":"Epidural hemorrhage"}]}},{"entity":"ClinVarVariant:53412","phenotype":{"types":[{"id":"HP:0001948","label":"Alkalosis"}]}},{"entity":"ClinVarVariant:189740","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:12016","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"MGI:4839231","phenotype":{"types":[{"id":"MP:0009977","label":"abnormal cerebellar granule cell migration"}]}},{"entity":"ClinVarVariant:50019","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:829","phenotype":{"types":[{"id":"HP:0000706","label":"Unerupted tooth"}]}},{"entity":"ClinVarVariant:66105","phenotype":{"types":[{"id":"HP:0001742","label":"Nasal obstruction"}]}},{"entity":"ClinVarVariant:10148","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"MGI:3510641","phenotype":{"types":[{"id":"MP:0003081","label":"abnormal soleus morphology"}]}},{"entity":"FlyBase:FBal0190270","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:204066","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:53902","phenotype":{"types":[{"id":"HP:0001082","label":"Cholecystitis"}]}},{"entity":"ClinVarVariant:18427","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00013144-WBRNAi00082701","phenotype":{"types":[{"id":"MP:0002209","label":"decreased germ cell number"}]}},{"entity":"ClinVarVariant:35733","phenotype":{"types":[{"id":"HP:0000934","label":"Chondrocalcinosis"}]}},{"entity":"ClinVarVariant:82630","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:11379","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:56465","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:48762","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:25036","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"ClinVarVariant:24670","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:162009","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:24292","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:189710","phenotype":{"types":[{"id":"HP:0000478","label":"Abnormality of the eye"}]}},{"entity":"AQTL:25469","phenotype":{"types":[{"id":"AQTLTrait:1044","label":"Milk yield"}]}},{"entity":"ClinVarVariant:24488","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:24581","phenotype":{"types":[{"id":"HP:0100586","label":"Aseptic leukocyturia"}]}},{"entity":"ClinVarVariant:183145","phenotype":{"types":[{"id":"HP:0010318","label":"Aplasia/Hypoplasia of the abdominal wall musculature"}]}},{"entity":"ClinVarVariant:49761","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:41939","phenotype":{"types":[{"id":"HP:0003741","label":"Congenital muscular dystrophy"}]}},{"entity":"ClinVarVariant:126837","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001929-WBRNAi00026532","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:97695","phenotype":{"types":[{"id":"HP:0100537","label":"Fasciitis"}]}},{"entity":"ClinVarVariant:139033","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:53744","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:9990","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"MGI:3811233","phenotype":{"types":[{"id":"MP:0000060","label":"delayed bone ossification"}]}},{"entity":"ClinVarVariant:92205","phenotype":{"types":[{"id":"HP:0000131","label":"Uterine leiomyoma"}]}},{"entity":"ClinVarVariant:53973","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:35456","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:55938","phenotype":{"types":[{"id":"HP:0006887","label":"Intellectual disability, progressive"}]}},{"entity":"ClinVarVariant:189683","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:143543","phenotype":{"types":[{"id":"HP:0010521","label":"Gait apraxia"}]}},{"entity":"ClinVarVariant:210299","phenotype":{"types":[{"id":"HP:0002592","label":"Gastric ulcer"}]}},{"entity":"ClinVarVariant:36794","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"ClinVarVariant:217164","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"AQTL:31966","phenotype":{"types":[{"id":"AQTLTrait:2161","label":"Femur length"}]}},{"entity":"ClinVarVariant:53219","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"ClinVarVariant:13325","phenotype":{"types":[{"id":"HP:0001644","label":"Dilated cardiomyopathy"}]}},{"entity":"ClinVarVariant:208080","phenotype":{"types":[{"id":"HP:0005478","label":"Prominent frontal sinuses"}]}},{"entity":"ClinVarVariant:42420","phenotype":{"types":[{"id":"HP:0000646","label":"Amblyopia"}]}},{"entity":"ClinVarVariant:35832","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"ClinVarVariant:36764","phenotype":{"types":[{"id":"HP:0006682","label":"Ventricular extrasystoles"}]}},{"entity":"ClinVarVariant:53493","phenotype":{"types":[{"id":"HP:0011109","label":"Chronic sinusitis"}]}},{"entity":"MGI:3590264","phenotype":{"types":[{"id":"MP:0001987","label":"alcohol preference"}]}},{"entity":"ClinVarVariant:6213","phenotype":{"types":[{"id":"HP:0003218","label":"Oroticaciduria"}]}},{"entity":"ClinVarVariant:53158","phenotype":{"types":[{"id":"HP:0004395","label":"Malnutrition"}]}},{"entity":"ClinVarVariant:188948","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00014883-WBRNAi00077884","phenotype":{"types":[{"id":"WBPhenotype:0001824","label":"meiotic progression prophase variant"}]}},{"entity":"ClinVarVariant:183330","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:41088","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:66501","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"MGI:2135666","phenotype":{"types":[{"id":"MP:0000166","label":"abnormal chondrocyte morphology"}]}},{"entity":"ClinVarVariant:2608","phenotype":{"types":[{"id":"HP:0011096","label":"Peripheral demyelination"}]}},{"entity":"ClinVarVariant:45017","phenotype":{"types":[{"id":"HP:0011663","label":"Right ventricular cardiomyopathy"}]}},{"entity":"ClinVarVariant:217252","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:6021","phenotype":{"types":[{"id":"HP:0002230","label":"Generalized hirsutism"}]}},{"entity":"ClinVarVariant:11755","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"MGI:2388715","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"MGI:4888719","phenotype":{"types":[{"id":"MP:0006060","label":"increased cerebral infarction size"}]}},{"entity":"ClinVarVariant:49751","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:162613","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:92705","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00016493-WBRNAi00096905","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"ClinVarVariant:36112","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:36577","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"FlyBase:FBal0209323","phenotype":{"types":[{"id":"FBcv:0000352","label":"partially lethal - majority die"}]}},{"entity":"ClinVarVariant:13162","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:25340","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:5509","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003084-WBRNAi00078913","phenotype":{"types":[{"id":"WBPhenotype:0000700","label":"multivulva"}]}},{"entity":"ClinVarVariant:211736","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"MGI:3775648","phenotype":{"types":[{"id":"HP:0012465","label":"Elevated hepatic iron concentration"}]}},{"entity":"ClinVarVariant:65274","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:11811","phenotype":{"types":[{"id":"HP:0000248","label":"Brachycephaly"}]}},{"entity":"ClinVarVariant:49741","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:158612","phenotype":{"types":[{"id":"HP:0007266","label":"Cerebral dysmyelination"}]}},{"entity":"MGI:2181021","phenotype":{"types":[{"id":"MP:0011086","label":"postnatal lethality, incomplete penetrance"}]}},{"entity":"MGI:4362924","phenotype":{"types":[{"id":"HP:0010976","label":"B lymphocytopenia"}]}},{"entity":"ClinVarVariant:2017","phenotype":{"types":[{"id":"HP:0000230","label":"Gingivitis"}]}},{"entity":"ClinVarVariant:2945","phenotype":{"types":[{"id":"HP:0000662","label":"Nyctalopia"}]}},{"entity":"ClinVarVariant:42325","phenotype":{"types":[{"id":"HP:0004933","label":"Ascending aortic dissection"}]}},{"entity":"WormBase:WBVar00252220","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:1451","phenotype":{"types":[{"id":"HP:0006597","label":"Diaphragmatic paralysis"}]}},{"entity":"ClinVarVariant:11082","phenotype":{"types":[{"id":"HP:0002361","label":"Psychomotor deterioration"}]}},{"entity":"ClinVarVariant:7192","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:5280","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:36102","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:2250","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"ClinVarVariant:101138","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"ClinVarVariant:10253","phenotype":{"types":[{"id":"HP:0005681","label":"Juvenile rheumatoid arthritis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00009882-WBRNAi00085534","phenotype":{"types":[{"id":"WBPhenotype:0001810","label":"oocyte septum formation variant"}]}},{"entity":"FlyBase:FBal0302452","phenotype":{"types":[{"id":"FBcv:0000316","label":"homeotic"}]}},{"entity":"ClinVarVariant:6810","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000962-WBRNAi00085605","phenotype":{"types":[{"id":"WBPhenotype:0001028","label":"nuclear appearance variant"}]}},{"entity":"ClinVarVariant:137950","phenotype":{"types":[{"id":"HP:0009765","label":"Low hanging columella"}]}},{"entity":"ClinVarVariant:53851","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:3670","phenotype":{"types":[{"id":"HP:0007957","label":"Corneal opacity"}]}},{"entity":"ClinVarVariant:143152","phenotype":{"types":[{"id":"HP:0002251","label":"Aganglionic megacolon"}]}},{"entity":"ClinVarVariant:162134","phenotype":{"types":[{"id":"HP:0007754","label":"Macular dystrophy"}]}},{"entity":"ClinVarVariant:211254","phenotype":{"types":[{"id":"HP:0001973","label":"Autoimmune thrombocytopenia"}]}},{"entity":"ClinVarVariant:167491","phenotype":{"types":[{"id":"HP:0002089","label":"Pulmonary hypoplasia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006928-WBRNAi00095274","phenotype":{"types":[{"id":"WBPhenotype:0001013","label":"pathogen susceptibility increased"}]}},{"entity":"ClinVarVariant:40678","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:42545","phenotype":{"types":[{"id":"HP:0000859","label":"Hyperaldosteronism"}]}},{"entity":"ClinVarVariant:180643","phenotype":{"types":[{"id":"HP:0002359","label":"Frequent falls"}]}},{"entity":"ClinVarVariant:65302","phenotype":{"types":[{"id":"HP:0000826","label":"Precocious puberty"}]}},{"entity":"ClinVarVariant:48947","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:4182","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:52338","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:41162","phenotype":{"types":[{"id":"HP:0003162","label":"Fasting hypoglycemia"}]}},{"entity":"MGI:2177337","phenotype":{"types":[{"id":"MP:0003934","label":"abnormal pancreas development"}]}},{"entity":"ClinVarVariant:2033","phenotype":{"types":[{"id":"HP:0000830","label":"Anterior hypopituitarism"}]}},{"entity":"ClinVarVariant:21244","phenotype":{"types":[{"id":"HP:0011362","label":"Abnormal hair quantity"}]}},{"entity":"MGI:2155977","phenotype":{"types":[{"id":"GO:0043066PHENOTYPE","label":"negative regulation of apoptotic process phenotype"}]}},{"entity":"ClinVarVariant:13903","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:184187","phenotype":{"types":[{"id":"HP:0005523","label":"Lymphoproliferative disorder"}]}},{"entity":"ClinVarVariant:126446","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:181723","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:3160","phenotype":{"types":[{"id":"HP:0001254","label":"Lethargy"}]}},{"entity":"ClinVarVariant:204097","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:10108","phenotype":{"types":[{"id":"HP:0005542","label":"Prolonged whole-blood clotting time"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000376-WBRNAi00027553","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"FlyBase:FBal0203410","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:49731","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:11736","phenotype":{"types":[{"id":"HP:0010808","label":"Protruding tongue"}]}},{"entity":"dbSNP:rs9268905","phenotype":{"types":[{"id":"HP:0002331","label":"Headache (with pheochromocytoma)"}]}},{"entity":"MGI:5548388","phenotype":{"types":[{"id":"HP:0005736","label":"Short tibia"}]}},{"entity":"WormBase:WBVar00242226","phenotype":{"types":[{"id":"WBPhenotype:0000470","label":"HSN migration variant"}]}},{"entity":"FlyBase:FBal0207110","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:41191","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:38985","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:204056","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:56302","phenotype":{"types":[{"id":"HP:0002323","label":"Anencephaly"}]}},{"entity":"ClinVarVariant:101279","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:196934","phenotype":{"types":[{"id":"HP:0002512","label":"Brain stem compression"}]}},{"entity":"MGI:2653045","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:4888","phenotype":{"types":[{"id":"HP:0100639","label":"Erectile abnormalities"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-990415-279-ZDB-MRPHLNO-070116-1","phenotype":{"types":[{"id":"GO:0021854PHENOTYPE","label":"hypothalamus development phenotype"}]}},{"entity":"ClinVarVariant:21595","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:41158","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"AQTL:15956","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:101279","phenotype":{"types":[{"id":"HP:0000015","label":"Bladder diverticulum"}]}},{"entity":"ClinVarVariant:13396","phenotype":{"types":[{"id":"HP:0007772","label":"Impaired smooth pursuit"}]}},{"entity":"ClinVarVariant:143704","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:5634328","phenotype":{"types":[{"id":"HP:0011970","label":"Cerebral amyloid angiopathy"}]}},{"entity":"AQTL:18099","phenotype":{"types":[{"id":"AQTLTrait:1153","label":"Stillbirth"}]}},{"entity":"ClinVarVariant:216145","phenotype":{"types":[{"id":"HP:0009806","label":"Nephrogenic diabetes insipidus"}]}},{"entity":"ClinVarVariant:53643","phenotype":{"types":[{"id":"HP:0100732","label":"Pancreatic fibrosis"}]}},{"entity":"ClinVarVariant:217069","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:1955","phenotype":{"types":[{"id":"HP:0001890","label":"Autoimmune hemolytic anemia"}]}},{"entity":"ClinVarVariant:39667","phenotype":{"types":[{"id":"HP:0006380","label":"Knee flexion contracture"}]}},{"entity":"AQTL:13689","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:209143","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:8762","phenotype":{"types":[{"id":"HP:0000988","label":"Skin rash"}]}},{"entity":"ZFIN:ZDB-ALT-050913-4","phenotype":{"types":[{"id":"ZP:0010859","label":"abnormal(ly) lacks parts or has fewer parts of type olfactory epithelium towards olfactory epithelium microvillous olfactory receptor neuron"}]}},{"entity":"ClinVarVariant:1221","phenotype":{"types":[{"id":"HP:0002063","label":"Rigidity"}]}},{"entity":"FlyBase:FBal0199572","phenotype":{"types":[{"id":"FBbt:00005169PHENOTYPE","label":"Drosophila trichogen cell phenotype"}]}},{"entity":"ClinVarVariant:7161","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"MGI:1931048","phenotype":{"types":[{"id":"GO:0001525PHENOTYPE","label":"angiogenesis phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001686-WBRNAi00023783","phenotype":{"types":[{"id":"WBPhenotype:0001183","label":"fat content reduced"}]}},{"entity":"ClinVarVariant:49805","phenotype":{"types":[{"id":"HP:0009720","label":"Adenoma sebaceum"}]}},{"entity":"ClinVarVariant:50874","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:53942","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"AQTL:20964","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"ClinVarVariant:183242","phenotype":{"types":[{"id":"HP:0003687","label":"Centrally nucleated skeletal muscle fibers"}]}},{"entity":"ClinVarVariant:21057","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:49848","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"MGI:4367072","phenotype":{"types":[{"id":"MP:0004753","label":"abnormal miniature excitatory postsynaptic currents"}]}},{"entity":"FlyBase:FBal0292824","phenotype":{"types":[{"id":"FBcv:0000366","label":"female sterile"}]}},{"entity":"FlyBase:FBal0130285","phenotype":{"types":[{"id":"FBcv:0000449","label":"planar polarity defective"}]}},{"entity":"ClinVarVariant:38887","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-001212-6-ZDB-MRPHLNO-060215-2","phenotype":{"types":[{"id":"ZP:0000955","label":"abnormal(ly) disrupted determination of heart left/right asymmetry"}]}},{"entity":"MGI:3528994","phenotype":{"types":[{"id":"MP:0005463","label":"abnormal CD4-positive, alpha-beta T cell physiology"}]}},{"entity":"ClinVarVariant:68698","phenotype":{"types":[{"id":"HP:0002900","label":"Hypokalemia"}]}},{"entity":"ClinVarVariant:53390","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:216707","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"ClinVarVariant:56027","phenotype":{"types":[{"id":"HP:0008434","label":"Hypoplastic cervical vertebrae"}]}},{"entity":"ClinVarVariant:126651","phenotype":{"types":[{"id":"HP:0000864","label":"Abnormality of the hypothalamus-pituitary axis"}]}},{"entity":"ClinVarVariant:82337","phenotype":{"types":[{"id":"HP:0006753","label":"Neoplasm of the stomach"}]}},{"entity":"dbSNP:rs29015207","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:4881","phenotype":{"types":[{"id":"HP:0000771","label":"Gynecomastia"}]}},{"entity":"ClinVarVariant:156326","phenotype":{"types":[{"id":"HP:0001762","label":"Talipes equinovarus"}]}},{"entity":"ClinVarVariant:3211","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007385-WBRNAi00028603","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"ClinVarVariant:92521","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"ClinVarVariant:10756","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"ClinVarVariant:11000","phenotype":{"types":[{"id":"HP:0002021","label":"Pyloric stenosis"}]}},{"entity":"MGI:3698867","phenotype":{"types":[{"id":"MP:0002047","label":"increased hepatic hemangioma incidence"}]}},{"entity":"ClinVarVariant:53648","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:53396","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:126952","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:135756","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:10194","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:204268","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:1641","phenotype":{"types":[{"id":"HP:0002942","label":"Thoracic kyphosis"}]}},{"entity":"WormBase:WBVar00089870","phenotype":{"types":[{"id":"WBPhenotype:0000425","label":"antibody staining reduced"}]}},{"entity":"ClinVarVariant:135702","phenotype":{"types":[{"id":"HP:0000684","label":"Delayed eruption of teeth"}]}},{"entity":"MGI:2137553","phenotype":{"types":[{"id":"MP:0001698","label":"decreased embryo size"}]}},{"entity":"MGI:1933761","phenotype":{"types":[{"id":"HP:0100522","label":"Thymoma"}]}},{"entity":"ClinVarVariant:135767","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:1391","phenotype":{"types":[{"id":"HP:0004639","label":"Elevated amniotic fluid alpha-fetoprotein"}]}},{"entity":"ClinVarVariant:49307","phenotype":{"types":[{"id":"HP:0009554","label":"Projection of scalp hair onto lateral cheek"}]}},{"entity":"MGI:5629408","phenotype":{"types":[{"id":"HP:0003097","label":"Short femur"}]}},{"entity":"ClinVarVariant:18334","phenotype":{"types":[{"id":"HP:0007110","label":"Central hypoventilation"}]}},{"entity":"_:genid1976156","phenotype":{"types":[{"id":"ZP:0000038","label":"abnormal(ly) edematous pericardium"}]}},{"entity":"ClinVarVariant:24775","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:9450","phenotype":{"types":[{"id":"HP:0000455","label":"Broad nasal tip"}]}},{"entity":"ClinVarVariant:204096","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:2764","phenotype":{"types":[{"id":"HP:0003019","label":"Abnormality of the wrist"}]}},{"entity":"ClinVarVariant:16814","phenotype":{"types":[{"id":"HP:0011663","label":"Right ventricular cardiomyopathy"}]}},{"entity":"ClinVarVariant:29667","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"ClinVarVariant:16303","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:181735","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:161992","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"ClinVarVariant:17272","phenotype":{"types":[{"id":"HP:0004277","label":"Fractured hand bones"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002202-WBRNAi00101493","phenotype":{"types":[{"id":"WBPhenotype:0001887","label":"excess seam cells"}]}},{"entity":"ClinVarVariant:13898","phenotype":{"types":[{"id":"HP:0001558","label":"Decreased fetal movement"}]}},{"entity":"ClinVarVariant:49526","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:24694","phenotype":{"types":[{"id":"HP:0011502","label":"Posterior lenticonus"}]}},{"entity":"FlyBase:FBal0204414","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:40983","phenotype":{"types":[{"id":"HP:0002757","label":"Recurrent fractures"}]}},{"entity":"ClinVarVariant:102723","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:14700","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:54043","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:55824","phenotype":{"types":[{"id":"HP:0001900","label":"Increased hemoglobin"}]}},{"entity":"ClinVarVariant:160314","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:159229","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:8882","phenotype":{"types":[{"id":"HP:0006989","label":"Dysplastic corpus callosum"}]}},{"entity":"ClinVarVariant:3167","phenotype":{"types":[{"id":"HP:0003419","label":"Low back pain"}]}},{"entity":"MGI:2152978","phenotype":{"types":[{"id":"HP:0008873","label":"Disproportionate short-limb short stature"}]}},{"entity":"ClinVarVariant:12975","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:127425","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:7519","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:54073","phenotype":{"types":[{"id":"HP:0006536","label":"Obstructive lung disease"}]}},{"entity":"ClinVarVariant:163768","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ZFIN:ZDB-ALT-980203-483","phenotype":{"types":[{"id":"ZP:0001317","label":"abnormal(ly) condensed pharyngeal arch cartilage"}]}},{"entity":"ClinVarVariant:192382","phenotype":{"types":[{"id":"HP:0000303","label":"Mandibular prognathia"}]}},{"entity":"ClinVarVariant:120303","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:157598","phenotype":{"types":[{"id":"HP:0001231","label":"Abnormality of the fingernails"}]}},{"entity":"MGI:3620559","phenotype":{"types":[{"id":"MP:0003719","label":"abnormal pericyte morphology"}]}},{"entity":"ClinVarVariant:216935","phenotype":{"types":[{"id":"HP:0000900","label":"Thickened ribs"}]}},{"entity":"ClinVarVariant:24548","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:143491","phenotype":{"types":[{"id":"HP:0010521","label":"Gait apraxia"}]}},{"entity":"MGI:3797077","phenotype":{"types":[{"id":"MP:0013283","label":"failure of ventral body wall closure"}]}},{"entity":"ClinVarVariant:8814","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:140832","phenotype":{"types":[{"id":"HP:0002344","label":"Progressive neurologic deterioration"}]}},{"entity":"MGI:2180365","phenotype":{"types":[{"id":"MP:0000097","label":"short maxilla"}]}},{"entity":"ClinVarVariant:56455","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:94811","phenotype":{"types":[{"id":"HP:0003713","label":"Muscle fiber necrosis"}]}},{"entity":"MGI:3579497","phenotype":{"types":[{"id":"MP:0001728","label":"failure of embryo implantation"}]}},{"entity":"ClinVarVariant:36113","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:7185","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"FlyBase:FBal0244010","phenotype":{"types":[{"id":"FBbt:00004283PHENOTYPE","label":"Drosophila prothoracic tarsal bristle phenotype"}]}},{"entity":"ClinVarVariant:101145","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:7444","phenotype":{"types":[{"id":"HP:0000771","label":"Gynecomastia"}]}},{"entity":"MGI:4457504","phenotype":{"types":[{"id":"HP:0003076","label":"Glycosuria"}]}},{"entity":"ClinVarVariant:50854","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"MGI:2449290","phenotype":{"types":[{"id":"HP:0100738","label":"Abnormal eating behavior"}]}},{"entity":"ClinVarVariant:5859","phenotype":{"types":[{"id":"HP:0000684","label":"Delayed eruption of teeth"}]}},{"entity":"ClinVarVariant:41151","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:1985","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:66441","phenotype":{"types":[{"id":"HP:0100707","label":"Abnormality of the astrocytes"}]}},{"entity":"MGI:2386172","phenotype":{"types":[{"id":"MP:0002118","label":"abnormal lipid homeostasis"}]}},{"entity":"ClinVarVariant:53972","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:42363","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"MGI:2150350","phenotype":{"types":[{"id":"HP:0001669","label":"Transposition of the great arteries"}]}},{"entity":"ClinVarVariant:127150","phenotype":{"types":[{"id":"HP:0001321","label":"Cerebellar hypoplasia"}]}},{"entity":"MGI:1855936","phenotype":{"types":[{"id":"HP:0009887","label":"Abnormality of hair pigmentation"}]}},{"entity":"_:genid1972365","phenotype":{"types":[{"id":"ZP:0014893","label":"abnormal(ly) process quality response to gamma radiation"}]}},{"entity":"ClinVarVariant:30547","phenotype":{"types":[{"id":"HP:0000972","label":"Palmoplantar hyperkeratosis"}]}},{"entity":"ClinVarVariant:53788","phenotype":{"types":[{"id":"HP:0100646","label":"Thyroiditis"}]}},{"entity":"MGI:3041864","phenotype":{"types":[{"id":"MP:0008395","label":"abnormal osteoblast differentiation"}]}},{"entity":"MGI:1856910","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:142043","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:216224","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:210843","phenotype":{"types":[{"id":"HP:0100495","label":"Mastocytosis"}]}},{"entity":"ClinVarVariant:25184","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:143181","phenotype":{"types":[{"id":"HP:0001123","label":"Visual field defect"}]}},{"entity":"FlyBase:FBal0198615","phenotype":{"types":[{"id":"FBcv:0000386","label":"long lived"}]}},{"entity":"ClinVarVariant:189163","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:41364","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:7945","phenotype":{"types":[{"id":"HP:0000077","label":"Abnormality of the kidney"}]}},{"entity":"MGI:3051523","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"FlyBase:FBal0213272","phenotype":{"types":[{"id":"FBcv:0000356","label":"body color defective"}]}},{"entity":"ClinVarVariant:9143","phenotype":{"types":[{"id":"HP:0003455","label":"Elevated long chain fatty acids"}]}},{"entity":"ClinVarVariant:35823","phenotype":{"types":[{"id":"HP:0001742","label":"Nasal obstruction"}]}},{"entity":"ClinVarVariant:10460","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:101300","phenotype":{"types":[{"id":"HP:0100784","label":"Peripheral arteriovenous fistula"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022281-WBRNAi00098373","phenotype":{"types":[{"id":"WBPhenotype:0001566","label":"ventral enclosure variant"}]}},{"entity":"AQTL:28586","phenotype":{"types":[{"id":"AQTLTrait:1169","label":"Interval to first estrus after calving"}]}},{"entity":"dbSNP:rs43697015","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:10723","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"AQTL:13101","phenotype":{"types":[{"id":"AQTLTrait:1110","label":"Muscle protein percentage"}]}},{"entity":"ClinVarVariant:53234","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:17380","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:133325","phenotype":{"types":[{"id":"HP:0002317","label":"Unsteady gait"}]}},{"entity":"ClinVarVariant:93761","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"MGI:5320677","phenotype":{"types":[{"id":"HP:0001899","label":"Increased hematocrit"}]}},{"entity":"ClinVarVariant:159128","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:49173","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:36035","phenotype":{"types":[{"id":"HP:0000541","label":"Retinal detachment"}]}},{"entity":"ClinVarVariant:209052","phenotype":{"types":[{"id":"HP:0002107","label":"Pneumothorax"}]}},{"entity":"ClinVarVariant:204278","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:13560","phenotype":{"types":[{"id":"HP:0001873","label":"Thrombocytopenia"}]}},{"entity":"ClinVarVariant:2456","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"MGI:5548068","phenotype":{"types":[{"id":"MP:0001265","label":"decreased body size"}]}},{"entity":"ClinVarVariant:834","phenotype":{"types":[{"id":"HP:0006000","label":"Ureteral obstruction"}]}},{"entity":"ClinVarVariant:1676","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"FlyBase:FBal0125280","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"dbSNP:rs41628993","phenotype":{"types":[{"id":"AQTLTrait:1067","label":"Length of productive life"}]}},{"entity":"ClinVarVariant:3445","phenotype":{"types":[{"id":"HP:0000085","label":"Horseshoe kidney"}]}},{"entity":"ClinVarVariant:101410","phenotype":{"types":[{"id":"HP:0000790","label":"Hematuria"}]}},{"entity":"ClinVarVariant:53404","phenotype":{"types":[{"id":"HP:0100512","label":"Vitamin D deficiency"}]}},{"entity":"ClinVarVariant:197210","phenotype":{"types":[{"id":"HP:0008261","label":"Pancreatic islet cell adenoma"}]}},{"entity":"MGI:2387852","phenotype":{"types":[{"id":"GO:0070192PHENOTYPE","label":"chromosome organization involved in meiosis phenotype"}]}},{"entity":"FlyBase:FBal0044814","phenotype":{"types":[{"id":"FBbt:00003479PHENOTYPE","label":"Drosophila abdominal ventral muscle phenotype"}]}},{"entity":"ClinVarVariant:177938","phenotype":{"types":[{"id":"HP:0100749","label":"Chest pain"}]}},{"entity":"ClinVarVariant:2139","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ClinVarVariant:24395","phenotype":{"types":[{"id":"HP:0000093","label":"Proteinuria"}]}},{"entity":"MGI:3696958","phenotype":{"types":[{"id":"HP:0100678","label":"Premature skin wrinkling"}]}},{"entity":"ClinVarVariant:36123","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:156339","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:67976","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:157934","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"ClinVarVariant:5408","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:30450","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000209-WBRNAi00073191","phenotype":{"types":[{"id":"WBPhenotype:0001037","label":"sterile progeny"}]}},{"entity":"ClinVarVariant:8814","phenotype":{"types":[{"id":"HP:0004964","label":"Pulmonary arterial medial hypertrophy"}]}},{"entity":"ClinVarVariant:6465","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"MGI:3047647","phenotype":{"types":[{"id":"GO:0043249PHENOTYPE","label":"erythrocyte maturation phenotype"}]}},{"entity":"FlyBase:FBal0204879","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:17309","phenotype":{"types":[{"id":"HP:0007759","label":"Opacification of the corneal stroma"}]}},{"entity":"ClinVarVariant:9368","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:126748","phenotype":{"types":[{"id":"HP:0100760","label":"Clubbing of toes"}]}},{"entity":"ClinVarVariant:161993","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"MGI:2156498","phenotype":{"types":[{"id":"MP:0011086","label":"postnatal lethality, incomplete penetrance"}]}},{"entity":"ClinVarVariant:428","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:53316","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:67838","phenotype":{"types":[{"id":"HP:0004756","label":"Ventricular tachycardia"}]}},{"entity":"ClinVarVariant:211468","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:158542","phenotype":{"types":[{"id":"HP:0010719","label":"Abnormality of hair texture"}]}},{"entity":"ClinVarVariant:158830","phenotype":{"types":[{"id":"HP:0008678","label":"Renal hypoplasia/aplasia"}]}},{"entity":"MGI:1858030","phenotype":{"types":[{"id":"MP:0000819","label":"abnormal olfactory bulb morphology"}]}},{"entity":"MGI:4421413","phenotype":{"types":[{"id":"HP:0011373","label":"Incomplete partition of the cochlea"}]}},{"entity":"ClinVarVariant:25287","phenotype":{"types":[{"id":"HP:0008209","label":"Premature ovarian failure"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004306-WBRNAi00027441","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:161401","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"ClinVarVariant:12010","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"ClinVarVariant:49791","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:49215","phenotype":{"types":[{"id":"HP:0009719","label":"Hypomelanotic macule"}]}},{"entity":"ClinVarVariant:94759","phenotype":{"types":[{"id":"HP:0001644","label":"Dilated cardiomyopathy"}]}},{"entity":"ClinVarVariant:4531","phenotype":{"types":[{"id":"HP:0000144","label":"Decreased fertility"}]}},{"entity":"ClinVarVariant:37353","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:97583","phenotype":{"types":[{"id":"HP:0005214","label":"Intestinal obstruction"}]}},{"entity":"ClinVarVariant:194555","phenotype":{"types":[{"id":"HP:0200134","label":"Epileptic encephalopathy"}]}},{"entity":"FlyBase:FBal0208599","phenotype":{"types":[{"id":"FBcv:0000393","label":"pain response defective"}]}},{"entity":"MGI:5295237","phenotype":{"types":[{"id":"MP:0008498","label":"decreased IgG3 level"}]}},{"entity":"ClinVarVariant:10606","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"MGI:3043578","phenotype":{"types":[{"id":"MP:0001382","label":"abnormal nursing"}]}},{"entity":"ClinVarVariant:10251","phenotype":{"types":[{"id":"HP:0100773","label":"Cartilage destruction"}]}},{"entity":"ClinVarVariant:97709","phenotype":{"types":[{"id":"HP:0001677","label":"Coronary artery disease"}]}},{"entity":"ClinVarVariant:53959","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ClinVarVariant:54093","phenotype":{"types":[{"id":"HP:0000966","label":"Hypohidrosis"}]}},{"entity":"ClinVarVariant:64918","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:4348","phenotype":{"types":[{"id":"HP:0002839","label":"Urinary bladder sphincter dysfunction"}]}},{"entity":"MGI:3610995","phenotype":{"types":[{"id":"MP:0002910","label":"abnormal excitatory postsynaptic currents"}]}},{"entity":"AQTL:55082","phenotype":{"types":[{"id":"AQTLTrait:1153","label":"Stillbirth"}]}},{"entity":"ClinVarVariant:4380","phenotype":{"types":[{"id":"HP:0001281","label":"Tetany"}]}},{"entity":"ClinVarVariant:198424","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"ClinVarVariant:188978","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:6029","phenotype":{"types":[{"id":"HP:0003693","label":"Distal amyotrophy"}]}},{"entity":"ClinVarVariant:5243","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:11483","phenotype":{"types":[{"id":"HP:0003462","label":"Elevated 8-dehydrocholesterol"}]}},{"entity":"ClinVarVariant:49772","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:41177","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"MGI:1857718","phenotype":{"types":[{"id":"MP:0003691","label":"abnormal microglial cell physiology"}]}},{"entity":"ClinVarVariant:158369","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:217105","phenotype":{"types":[{"id":"HP:0001012","label":"Multiple lipomas"}]}},{"entity":"ClinVarVariant:55823","phenotype":{"types":[{"id":"HP:0000864","label":"Abnormality of the hypothalamus-pituitary axis"}]}},{"entity":"ClinVarVariant:14364","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"ClinVarVariant:127699","phenotype":{"types":[{"id":"HP:0002576","label":"Intussusception"}]}},{"entity":"ClinVarVariant:66051","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:4868762","phenotype":{"types":[{"id":"MP:0000428","label":"abnormal craniofacial morphology"}]}},{"entity":"ClinVarVariant:4305","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"MGI:3717494","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"WormBase:WBVar00142947","phenotype":{"types":[{"id":"WBPhenotype:0000644","label":"paralyzed"}]}},{"entity":"dbSNP:rs1896295","phenotype":{"types":[{"id":"HP:0002754","label":"Osteomyelitis"}]}},{"entity":"ClinVarVariant:65505","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:333","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:11675","phenotype":{"types":[{"id":"HP:0000233","label":"Thin vermilion border"}]}},{"entity":"ClinVarVariant:204117","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:8804","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:64705","phenotype":{"types":[{"id":"HP:0009716","label":"Subependymal nodules"}]}},{"entity":"dbSNP:rs1427407","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"FlyBase:FBal0285746","phenotype":{"types":[{"id":"FBbt:00005201PHENOTYPE","label":"denticle belt phenotype"}]}},{"entity":"ClinVarVariant:217428","phenotype":{"types":[{"id":"HP:0001231","label":"Abnormality of the fingernails"}]}},{"entity":"ClinVarVariant:95624","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ZFIN:ZDB-ALT-020426-56","phenotype":{"types":[{"id":"GO:0060036PHENOTYPE","label":"notochord cell vacuolation phenotype"}]}},{"entity":"dbSNP:rs11986414","phenotype":{"types":[{"id":"HP:0002756","label":"Pathologic fracture"}]}},{"entity":"ClinVarVariant:188893","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"ClinVarVariant:7404","phenotype":{"types":[{"id":"HP:0002226","label":"White eyebrow"}]}},{"entity":"ClinVarVariant:25390","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"dbSNP:rs3105491","phenotype":{"types":[{"id":"HP:0004825","label":"Increased hemoglobin oxygen affinity"}]}},{"entity":"ClinVarVariant:204086","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:49792","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:136076","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003992-WBRNAi00084326","phenotype":{"types":[{"id":"WBPhenotype:0000061","label":"extended life span"}]}},{"entity":"ClinVarVariant:38917","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:8137","phenotype":{"types":[{"id":"HP:0001002","label":"Decreased subcutaneous fat"}]}},{"entity":"ClinVarVariant:16085","phenotype":{"types":[{"id":"HP:0000055","label":"Abnormality of female external genitalia"}]}},{"entity":"ClinVarVariant:11362","phenotype":{"types":[{"id":"HP:0200042","label":"Skin ulcer"}]}},{"entity":"ClinVarVariant:101206","phenotype":{"types":[{"id":"HP:0000023","label":"Inguinal hernia"}]}},{"entity":"ClinVarVariant:53224","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:39727","phenotype":{"types":[{"id":"HP:0002239","label":"Gastrointestinal hemorrhage"}]}},{"entity":"ClinVarVariant:21106","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:91405","phenotype":{"types":[{"id":"HP:0002472","label":"Small cerebral cortex"}]}},{"entity":"FlyBase:FBal0144279","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011897-WBRNAi00095734","phenotype":{"types":[{"id":"WBPhenotype:0000402","label":"avoids bacterial lawn"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008149-WBRNAi00029911","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"ClinVarVariant:161364","phenotype":{"types":[{"id":"HP:0002486","label":"Myotonia"}]}},{"entity":"ClinVarVariant:2249","phenotype":{"types":[{"id":"HP:0001287","label":"Meningitis"}]}},{"entity":"FlyBase:FBal0270164","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:56689","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:102786","phenotype":{"types":[{"id":"HP:0005599","label":"Hypopigmentation of hair"}]}},{"entity":"ClinVarVariant:25221","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"AQTL:39589","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"dbSNP:rs10005603","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:35514","phenotype":{"types":[{"id":"HP:0000622","label":"Blurred vision"}]}},{"entity":"ClinVarVariant:179339","phenotype":{"types":[{"id":"HP:0001696","label":"Situs inversus totalis"}]}},{"entity":"ClinVarVariant:52328","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"dbSNP:rs6545883","phenotype":{"types":[{"id":"HP:0008207","label":"Primary adrenal insufficiency"}]}},{"entity":"AQTL:16175","phenotype":{"types":[{"id":"AQTLTrait:1044","label":"Milk yield"}]}},{"entity":"WormBase:WBVar00242144","phenotype":{"types":[{"id":"WBPhenotype:0000116","label":"mid larval lethal"}]}},{"entity":"ClinVarVariant:53973","phenotype":{"types":[{"id":"HP:0100582","label":"Nasal polyposis"}]}},{"entity":"ClinVarVariant:10872","phenotype":{"types":[{"id":"HP:0000286","label":"Epicanthus"}]}},{"entity":"ClinVarVariant:159191","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"ClinVarVariant:210786","phenotype":{"types":[{"id":"HP:0005306","label":"Capillary hemangiomas"}]}},{"entity":"ClinVarVariant:133075","phenotype":{"types":[{"id":"HP:0003738","label":"Exercise-induced myalgia"}]}},{"entity":"ClinVarVariant:211503","phenotype":{"types":[{"id":"HP:0000171","label":"Microglossia"}]}},{"entity":"ClinVarVariant:21274","phenotype":{"types":[{"id":"HP:0002827","label":"Hip dislocation"}]}},{"entity":"ClinVarVariant:14662","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:189027","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"MGI:3777553","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:16869","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ZFIN:ZDB-ALT-090625-1","phenotype":{"types":[{"id":"ZP:0004126","label":"abnormal(ly) absent intrahepatic bile duct"}]}},{"entity":"ClinVarVariant:35575","phenotype":{"types":[{"id":"HP:0001061","label":"Acne"}]}},{"entity":"ClinVarVariant:41181","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:7435","phenotype":{"types":[{"id":"HP:0000581","label":"Blepharophimosis"}]}},{"entity":"ClinVarVariant:56414","phenotype":{"types":[{"id":"HP:0003452","label":"Increased serum iron"}]}},{"entity":"ClinVarVariant:11159","phenotype":{"types":[{"id":"HP:0011948","label":"Acute respiratory tract infection"}]}},{"entity":"MGI:5311612","phenotype":{"types":[{"id":"MP:0002080","label":"prenatal lethality"}]}},{"entity":"ClinVarVariant:5116","phenotype":{"types":[{"id":"HP:0002857","label":"Genu valgum"}]}},{"entity":"ClinVarVariant:198034","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"FlyBase:FBal0244011","phenotype":{"types":[{"id":"FBbt:00004233PHENOTYPE","label":"Drosophila tertiary pigment cell phenotype"}]}},{"entity":"ClinVarVariant:97913","phenotype":{"types":[{"id":"HP:0001917","label":"Renal amyloidosis"}]}},{"entity":"ClinVarVariant:159983","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"ClinVarVariant:157955","phenotype":{"types":[{"id":"HP:0100022","label":"Abnormality of movement"}]}},{"entity":"ClinVarVariant:38312","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:158564","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"MGI:2674291","phenotype":{"types":[{"id":"MP:0000031","label":"abnormal cochlea morphology"}]}},{"entity":"ClinVarVariant:7230","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"NCBIGene:7467","phenotype":{"types":[{"id":"HP:0009778","label":"Short thumb"}]}},{"entity":"ClinVarVariant:56562","phenotype":{"types":[{"id":"HP:0000457","label":"Depressed nasal ridge"}]}},{"entity":"ClinVarVariant:155828","phenotype":{"types":[{"id":"HP:0000189","label":"Narrow palate"}]}},{"entity":"ClinVarVariant:182975","phenotype":{"types":[{"id":"HP:0002666","label":"Pheochromocytoma"}]}},{"entity":"FlyBase:FBal0206553","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:53925","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"NCBIGene:140906","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"FlyBase:FBal0159762","phenotype":{"types":[{"id":"FBbt:00005838PHENOTYPE","label":"NMJ bouton phenotype"}]}},{"entity":"ClinVarVariant:96117","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:14347","phenotype":{"types":[{"id":"HP:0002013","label":"Vomiting"}]}},{"entity":"ClinVarVariant:41334","phenotype":{"types":[{"id":"HP:0007067","label":"Distal peripheral sensory neuropathy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019801-WBRNAi00082236","phenotype":{"types":[{"id":"WBPhenotype:0001541","label":"dauer gonad arrest variant"}]}},{"entity":"ClinVarVariant:49738","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"MGI:2388352","phenotype":{"types":[{"id":"MP:0001274","label":"curly vibrissae"}]}},{"entity":"MGI:3690317","phenotype":{"types":[{"id":"HP:0012184","label":"Hyperalphalipoproteinemia"}]}},{"entity":"ClinVarVariant:159478","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"ClinVarVariant:4296","phenotype":{"types":[{"id":"HP:0011857","label":"Plasmacytoma"}]}},{"entity":"ClinVarVariant:53697","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019268-WBRNAi00008936","phenotype":{"types":[{"id":"WBPhenotype:0000032","label":"sick"}]}},{"entity":"ClinVarVariant:181743","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:1381","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"MGI:5520177","phenotype":{"types":[{"id":"HP:0000752","label":"Hyperactivity"}]}},{"entity":"FlyBase:FBal0208692","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:4613","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"MGI:1857196","phenotype":{"types":[{"id":"MP:0006082","label":"CNS inflammation"}]}},{"entity":"ClinVarVariant:216024","phenotype":{"types":[{"id":"HP:0002073","label":"Progressive cerebellar ataxia"}]}},{"entity":"ClinVarVariant:101299","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:36103","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:36315","phenotype":{"types":[{"id":"HP:0001025","label":"Urticaria"}]}},{"entity":"ClinVarVariant:181495","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:11362","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"FlyBase:FBal0147448","phenotype":{"types":[{"id":"FBcv:0000414","label":"locomotor behavior defective"}]}},{"entity":"ClinVarVariant:180350","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:1185","phenotype":{"types":[{"id":"HP:0000013","label":"Hypoplasia of the uterus"}]}},{"entity":"FlyBase:FBal0305239","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"dbSNP:rs41648982","phenotype":{"types":[{"id":"AQTLTrait:1120","label":"Thurl width"}]}},{"entity":"ClinVarVariant:159128","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"ClinVarVariant:6097","phenotype":{"types":[{"id":"HP:0006315","label":"Single median maxillary incisor"}]}},{"entity":"ClinVarVariant:10219","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:188945","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:101148","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00014088-WBRNAi00027107","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:53370","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:38995","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"dbSNP:rs109034504","phenotype":{"types":[{"id":"AQTLTrait:1070","label":"Inseminations per conception"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003026-WBRNAi00085490","phenotype":{"types":[{"id":"WBPhenotype:0001973","label":"germ cell compartment size variant"}]}},{"entity":"ClinVarVariant:18346","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:6094","phenotype":{"types":[{"id":"HP:0000748","label":"Inappropriate laughter"}]}},{"entity":"ClinVarVariant:56708","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"FlyBase:FBal0181584","phenotype":{"types":[{"id":"FBcv:0000450","label":"developmental rate defective"}]}},{"entity":"ClinVarVariant:159663","phenotype":{"types":[{"id":"HP:0006461","label":"Proximal femoral epiphysiolysis"}]}},{"entity":"MGI:104735","phenotype":{"types":[{"id":"MP:0002169","label":"no abnormal phenotype detected"}]}},{"entity":"ClinVarVariant:30538","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:17168","phenotype":{"types":[{"id":"HP:0006149","label":"Increased laxity of fingers"}]}},{"entity":"FlyBase:FBal0058344","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:21208","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:29973","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:2618","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:68708","phenotype":{"types":[{"id":"HP:0002900","label":"Hypokalemia"}]}},{"entity":"MGI:3620798","phenotype":{"types":[{"id":"MP:0002410","label":"decreased susceptibility to viral infection"}]}},{"entity":"MGI:3774341","phenotype":{"types":[{"id":"MP:0003203","label":"increased neuron apoptosis"}]}},{"entity":"ClinVarVariant:6552","phenotype":{"types":[{"id":"HP:0002213","label":"Fine hair"}]}},{"entity":"ClinVarVariant:56706","phenotype":{"types":[{"id":"HP:0002074","label":"Increased neuronal autofluorescent lipopigment"}]}},{"entity":"ClinVarVariant:40494","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"ClinVarVariant:10299","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:3050446","phenotype":{"types":[{"id":"MP:0004564","label":"enlarged myocardial fiber"}]}},{"entity":"ClinVarVariant:209062","phenotype":{"types":[{"id":"HP:0002107","label":"Pneumothorax"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001031-WBRNAi00072843","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:53980","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"ClinVarVariant:36058","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"AQTL:16912","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:211716","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:9319","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:30750","phenotype":{"types":[{"id":"HP:0003228","label":"Hypernatremia"}]}},{"entity":"ClinVarVariant:188958","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:211640","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:35842","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"ClinVarVariant:162384","phenotype":{"types":[{"id":"HP:0008070","label":"Sparse hair"}]}},{"entity":"MGI:5430994","phenotype":{"types":[{"id":"HP:0005576","label":"Tubulointerstitial fibrosis"}]}},{"entity":"ClinVarVariant:5645","phenotype":{"types":[{"id":"HP:0030507","label":"Retinal crystals"}]}},{"entity":"ClinVarVariant:40164","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00077457-WBRNAi00063328","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:14209","phenotype":{"types":[{"id":"HP:0000960","label":"Sacral dimple"}]}},{"entity":"ClinVarVariant:14097","phenotype":{"types":[{"id":"HP:0001712","label":"Left ventricular hypertrophy"}]}},{"entity":"ClinVarVariant:198504","phenotype":{"types":[{"id":"HP:0008443","label":"Spinal deformities"}]}},{"entity":"MGI:3695137","phenotype":{"types":[{"id":"MP:0005463","label":"abnormal CD4-positive, alpha-beta T cell physiology"}]}},{"entity":"ClinVarVariant:6067","phenotype":{"types":[{"id":"HP:0200055","label":"Small hand"}]}},{"entity":"ClinVarVariant:2669","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:97554","phenotype":{"types":[{"id":"HP:0000999","label":"Pyoderma"}]}},{"entity":"ClinVarVariant:24752","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:67777","phenotype":{"types":[{"id":"HP:0001696","label":"Situs inversus totalis"}]}},{"entity":"ClinVarVariant:6820","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"AQTL:41673","phenotype":{"types":[{"id":"AQTLTrait:1136","label":"Bone quality"}]}},{"entity":"ClinVarVariant:14209","phenotype":{"types":[{"id":"HP:0001875","label":"Neutropenia"}]}},{"entity":"ClinVarVariant:36946","phenotype":{"types":[{"id":"HP:0001915","label":"Aplastic anemia"}]}},{"entity":"ClinVarVariant:210456","phenotype":{"types":[{"id":"HP:0003819","label":"Death in childhood"}]}},{"entity":"ClinVarVariant:30945","phenotype":{"types":[{"id":"HP:0000388","label":"Otitis media"}]}},{"entity":"ClinVarVariant:49452","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:181763","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:6625","phenotype":{"types":[{"id":"HP:0000998","label":"Hypertrichosis"}]}},{"entity":"ClinVarVariant:83156","phenotype":{"types":[{"id":"HP:0006740","label":"Transitional cell carcinoma of the bladder"}]}},{"entity":"ClinVarVariant:36913","phenotype":{"types":[{"id":"HP:0002664","label":"Neoplasm"}]}},{"entity":"ClinVarVariant:42284","phenotype":{"types":[{"id":"HP:0004935","label":"Pulmonary artery atresia"}]}},{"entity":"MGI:1888408","phenotype":{"types":[{"id":"MP:0005641","label":"increased mean corpuscular hemoglobin concentration"}]}},{"entity":"ClinVarVariant:17696","phenotype":{"types":[{"id":"HP:0004370","label":"Abnormality of temperature regulation"}]}},{"entity":"ClinVarVariant:211746","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:25350","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:53346","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:13346","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"FlyBase:FBal0205447","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:65275","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"ClinVarVariant:53784","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:16623","phenotype":{"types":[{"id":"HP:0001371","label":"Flexion contracture"}]}},{"entity":"ClinVarVariant:48902","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"ClinVarVariant:189811","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:53373","phenotype":{"types":[{"id":"HP:0006706","label":"Cystic liver disease"}]}},{"entity":"ClinVarVariant:53337","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"MGI:4868451","phenotype":{"types":[{"id":"GO:0021697PHENOTYPE","label":"cerebellar cortex formation phenotype"}]}},{"entity":"AQTL:27090","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:92715","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:91403","phenotype":{"types":[{"id":"HP:0008678","label":"Renal hypoplasia/aplasia"}]}},{"entity":"ClinVarVariant:42015","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:68718","phenotype":{"types":[{"id":"HP:0002900","label":"Hypokalemia"}]}},{"entity":"ClinVarVariant:136097","phenotype":{"types":[{"id":"HP:0001166","label":"Arachnodactyly"}]}},{"entity":"ClinVarVariant:93448","phenotype":{"types":[{"id":"HP:0003271","label":"Visceromegaly"}]}},{"entity":"ClinVarVariant:10158","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"ClinVarVariant:188958","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"FlyBase:FBal0093398","phenotype":{"types":[{"id":"FBbt:00007115PHENOTYPE","label":"embryonic/larval neuroblast phenotype"}]}},{"entity":"ClinVarVariant:6066","phenotype":{"types":[{"id":"HP:0011318","label":"Bicoronal synostosis"}]}},{"entity":"ClinVarVariant:12534","phenotype":{"types":[{"id":"HP:0004493","label":"Craniofacial hyperostosis"}]}},{"entity":"ClinVarVariant:25214","phenotype":{"types":[{"id":"HP:0010741","label":"Edema of the lower limbs"}]}},{"entity":"FlyBase:FBal0263650","phenotype":{"types":[{"id":"FBbt:00004193PHENOTYPE","label":"cone cell phenotype"}]}},{"entity":"ClinVarVariant:53702","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"ClinVarVariant:2691","phenotype":{"types":[{"id":"HP:0011073","label":"Abnormality of dental color"}]}},{"entity":"ClinVarVariant:2143","phenotype":{"types":[{"id":"HP:0003083","label":"Dislocated radial head"}]}},{"entity":"ClinVarVariant:54083","phenotype":{"types":[{"id":"HP:0004401","label":"Meconium ileus"}]}},{"entity":"ClinVarVariant:35862","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"ClinVarVariant:158299","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:11515","phenotype":{"types":[{"id":"HP:0004594","label":"Hump-shaped mound of bone in central and posterior portions of vertebral endplate"}]}},{"entity":"ClinVarVariant:189750","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:16425","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"ClinVarVariant:60494","phenotype":{"types":[{"id":"HP:0002652","label":"Skeletal dysplasia"}]}},{"entity":"ClinVarVariant:216824","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:12281","phenotype":{"types":[{"id":"HP:0002908","label":"Conjugated hyperbilirubinemia"}]}},{"entity":"AQTL:46013","phenotype":{"types":[{"id":"AQTLTrait:1115","label":"Chest width"}]}},{"entity":"ClinVarVariant:135760","phenotype":{"types":[{"id":"HP:0012189","label":"Hodgkin lymphoma"}]}},{"entity":"MGI:5510759","phenotype":{"types":[{"id":"MP:0004794","label":"increased anti-nuclear antigen antibody level"}]}},{"entity":"MGI:2679886","phenotype":{"types":[{"id":"HP:0002011","label":"Morphological abnormality of the central nervous system"}]}},{"entity":"MGI:1857437","phenotype":{"types":[{"id":"MP:0003477","label":"abnormal nerve fiber response"}]}},{"entity":"MGI:1931041","phenotype":{"types":[{"id":"MP:0013164","label":"abnormal forelimb bud morphology"}]}},{"entity":"ClinVarVariant:56445","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:21512","phenotype":{"types":[{"id":"HP:0003233","label":"Hypoalphalipoproteinemia"}]}},{"entity":"ClinVarVariant:50091","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:2149","phenotype":{"types":[{"id":"HP:0000089","label":"Renal hypoplasia"}]}},{"entity":"ClinVarVariant:143395","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:30199","phenotype":{"types":[{"id":"HP:0001220","label":"Interphalangeal joint contracture of finger"}]}},{"entity":"ClinVarVariant:12524","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:36101","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:139581","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"ClinVarVariant:211726","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"FlyBase:FBal0150725","phenotype":{"types":[{"id":"FBbt:00003361PHENOTYPE","label":"indirect flight muscle phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019218-WBRNAi00086983","phenotype":{"types":[{"id":"WBPhenotype:0000038","label":"exploded through vulva"}]}},{"entity":"ClinVarVariant:216978","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"FlyBase:FBal0189919","phenotype":{"types":[{"id":"FBcv:0000356","label":"body color defective"}]}},{"entity":"ClinVarVariant:12048","phenotype":{"types":[{"id":"HP:0004947","label":"Arteriovenous fistula"}]}},{"entity":"ClinVarVariant:25350","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:5983","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:9521","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:5198","phenotype":{"types":[{"id":"HP:0100261","label":"Abnormal tendon morphology"}]}},{"entity":"ClinVarVariant:179126","phenotype":{"types":[{"id":"HP:0003805","label":"Rimmed vacuoles"}]}},{"entity":"MGI:1857150","phenotype":{"types":[{"id":"MP:0006413","label":"increased T cell apoptosis"}]}},{"entity":"MGI:3833397","phenotype":{"types":[{"id":"HP:0100763","label":"Abnormality of the lymphatic system"}]}},{"entity":"ClinVarVariant:3364","phenotype":{"types":[{"id":"HP:0200040","label":"Epidermoid cyst"}]}},{"entity":"MGI:3613611","phenotype":{"types":[{"id":"MP:0002836","label":"abnormal chorion morphology"}]}},{"entity":"ClinVarVariant:50874","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"FlyBase:FBal0283530","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"AQTL:50857","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"dbSNP:rs12386026","phenotype":{"types":[{"id":"HP:0001510","label":"Growth delay"}]}},{"entity":"ClinVarVariant:30725","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:11422","phenotype":{"types":[{"id":"HP:0011003","label":"Severe Myopia"}]}},{"entity":"ClinVarVariant:2915","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1443","phenotype":{"types":[{"id":"ZP:0001246","label":"abnormal(ly) morphology inner ear"}]}},{"entity":"MGI:2387973","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:53725","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"MGI:2386460","phenotype":{"types":[{"id":"MP:0000880","label":"decreased Purkinje cell number"}]}},{"entity":"ClinVarVariant:189842","phenotype":{"types":[{"id":"HP:0002384","label":"Focal seizures with impairment of consciousness or awareness"}]}},{"entity":"ClinVarVariant:162019","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:9590","phenotype":{"types":[{"id":"HP:0000762","label":"Decreased nerve conduction velocity"}]}},{"entity":"ClinVarVariant:53660","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"MGI:3628446","phenotype":{"types":[{"id":"MP:0004379","label":"wide frontal bone"}]}},{"entity":"ClinVarVariant:16330","phenotype":{"types":[{"id":"HP:0000256","label":"Macrocephaly"}]}},{"entity":"ClinVarVariant:2577","phenotype":{"types":[{"id":"HP:0000660","label":"Lipemia retinalis"}]}},{"entity":"ClinVarVariant:157514","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"ClinVarVariant:2627","phenotype":{"types":[{"id":"HP:0010743","label":"Short metatarsal"}]}},{"entity":"ClinVarVariant:10194","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:88859","phenotype":{"types":[{"id":"HP:0000091","label":"Abnormality of the renal tubule"}]}},{"entity":"ClinVarVariant:56718","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"ClinVarVariant:53254","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:3792","phenotype":{"types":[{"id":"HP:0001022","label":"Albinism"}]}},{"entity":"ClinVarVariant:53912","phenotype":{"types":[{"id":"HP:0001082","label":"Cholecystitis"}]}},{"entity":"ClinVarVariant:42566","phenotype":{"types":[{"id":"HP:0001297","label":"Stroke"}]}},{"entity":"ClinVarVariant:10669","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:6895","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"ClinVarVariant:12414","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"WormBase:WBVar01473710","phenotype":{"types":[{"id":"WBPhenotype:0000643","label":"locomotion variant"}]}},{"entity":"ClinVarVariant:182828","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:7984","phenotype":{"types":[{"id":"HP:0003189","label":"Long nose"}]}},{"entity":"ClinVarVariant:186330","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"MGI:3702746","phenotype":{"types":[{"id":"HP:0012087","label":"Abnormal mitochondrial shape"}]}},{"entity":"ClinVarVariant:216684","phenotype":{"types":[{"id":"HP:0000020","label":"Urinary incontinence"}]}},{"entity":"ClinVarVariant:65134","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:65092","phenotype":{"types":[{"id":"HP:0009719","label":"Hypomelanotic macule"}]}},{"entity":"ClinVarVariant:101385","phenotype":{"types":[{"id":"HP:0005293","label":"Venous insufficiency"}]}},{"entity":"ClinVarVariant:159912","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:181753","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"WormBase:WBVar00240990","phenotype":{"types":[{"id":"MP:0002209","label":"decreased germ cell number"}]}},{"entity":"ClinVarVariant:21729","phenotype":{"types":[{"id":"HP:0001080","label":"Biliary tract abnormality"}]}},{"entity":"ClinVarVariant:180360","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:53458","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"ClinVarVariant:6668","phenotype":{"types":[{"id":"HP:0009025","label":"Increased connective tissue"}]}},{"entity":"ClinVarVariant:2086","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"AQTL:12518","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"ClinVarVariant:54185","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:3965","phenotype":{"types":[{"id":"HP:0007633","label":"Bilateral microphthalmos"}]}},{"entity":"AQTL:26646","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:210770","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:166724","phenotype":{"types":[{"id":"HP:0003774","label":"Stage 5 chronic kidney disease"}]}},{"entity":"ClinVarVariant:143294","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"ClinVarVariant:36126","phenotype":{"types":[{"id":"HP:0008132","label":"Medial rotation of the medial malleolus"}]}},{"entity":"ClinVarVariant:36092","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:53574","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"ClinVarVariant:158741","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:12780","phenotype":{"types":[{"id":"HP:0006880","label":"Cerebellar hemangioblastoma"}]}},{"entity":"ClinVarVariant:21545","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1436","phenotype":{"types":[{"id":"ZP:0007196","label":"abnormal(ly) structure optic tract"}]}},{"entity":"ClinVarVariant:167709","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:35830","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:49922","phenotype":{"types":[{"id":"HP:0006772","label":"Renal angiomyolipoma"}]}},{"entity":"ClinVarVariant:6384","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"MGI:1933835","phenotype":{"types":[{"id":"MP:0010500","label":"myocardium hypoplasia"}]}},{"entity":"MGI:1857208","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:67907","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"FlyBase:FBal0210831","phenotype":{"types":[{"id":"FBcv:0000665","label":"body size defective"}]}},{"entity":"ClinVarVariant:136160","phenotype":{"types":[{"id":"HP:0001679","label":"Abnormality of the aorta"}]}},{"entity":"AQTL:39150","phenotype":{"types":[{"id":"AQTLTrait:1096","label":"Teat length"}]}},{"entity":"ClinVarVariant:48426","phenotype":{"types":[{"id":"HP:0010780","label":"Hyperacusis"}]}},{"entity":"ClinVarVariant:100768","phenotype":{"types":[{"id":"HP:0011448","label":"Ankle clonus"}]}},{"entity":"ClinVarVariant:158764","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"dbSNP:rs1934954","phenotype":{"types":[{"id":"HP:0000988","label":"Skin rash"}]}},{"entity":"ClinVarVariant:53774","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:1965","phenotype":{"types":[{"id":"HP:0001890","label":"Autoimmune hemolytic anemia"}]}},{"entity":"ClinVarVariant:215590","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:6542","phenotype":{"types":[{"id":"HP:0002213","label":"Fine hair"}]}},{"entity":"ClinVarVariant:39867","phenotype":{"types":[{"id":"HP:0002910","label":"Elevated hepatic transaminases"}]}},{"entity":"ClinVarVariant:53327","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"ClinVarVariant:14005","phenotype":{"types":[{"id":"HP:0100783","label":"Breast aplasia"}]}},{"entity":"ClinVarVariant:189048","phenotype":{"types":[{"id":"HP:0005598","label":"Facial telangiectasia in butterfly midface distribution"}]}},{"entity":"ZFIN:ZDB-ALT-051223-6","phenotype":{"types":[{"id":"ZP:0011581","label":"abnormal(ly) malformed post-vent vasculature"}]}},{"entity":"ClinVarVariant:16685","phenotype":{"types":[{"id":"HP:0002027","label":"Abdominal pain"}]}},{"entity":"ClinVarVariant:9659","phenotype":{"types":[{"id":"HP:0002891","label":"Uterine leiomyosarcoma"}]}},{"entity":"MGI:1857211","phenotype":{"types":[{"id":"MP:0008070","label":"absent T cells"}]}},{"entity":"ClinVarVariant:13370","phenotype":{"types":[{"id":"HP:0001894","label":"Thrombocytosis"}]}},{"entity":"ClinVarVariant:53565","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"ClinVarVariant:216937","phenotype":{"types":[{"id":"HP:0006960","label":"Choroid plexus calcification"}]}},{"entity":"MGI:3529581","phenotype":{"types":[{"id":"MP:0009967","label":"abnormal neuron proliferation"}]}},{"entity":"MGI:2156458","phenotype":{"types":[{"id":"HP:0006270","label":"Hypoplastic spleen"}]}},{"entity":"ClinVarVariant:68700","phenotype":{"types":[{"id":"HP:0000843","label":"Hyperparathyroidism"}]}},{"entity":"ClinVarVariant:53326","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:161123","phenotype":{"types":[{"id":"HP:0000496","label":"Abnormality of eye movement"}]}},{"entity":"ClinVarVariant:10486","phenotype":{"types":[{"id":"HP:0001922","label":"Vacuolated lymphocytes"}]}},{"entity":"ClinVarVariant:53236","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:24442","phenotype":{"types":[{"id":"HP:0008619","label":"Bilateral sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:4617","phenotype":{"types":[{"id":"HP:0003390","label":"Sensory axonal neuropathy"}]}},{"entity":"ClinVarVariant:101415","phenotype":{"types":[{"id":"HP:0000963","label":"Thin skin"}]}},{"entity":"FlyBase:FBal0239918","phenotype":{"types":[{"id":"FBcv:0000408","label":"stress response defective"}]}},{"entity":"ClinVarVariant:42377","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"dbSNP:rs110204815","phenotype":{"types":[{"id":"AQTLTrait:1081","label":"Age at puberty"}]}},{"entity":"ClinVarVariant:3694","phenotype":{"types":[{"id":"HP:0001114","label":"Xanthelasma"}]}},{"entity":"FlyBase:FBal0038994","phenotype":{"types":[{"id":"FBbt:00002142PHENOTYPE","label":"Drosophila metathoracic intersegmental nerve phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008852-WBRNAi00093225","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"ClinVarVariant:35521","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:36133","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:181833","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"ClinVarVariant:25300","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"AQTL:23571","phenotype":{"types":[{"id":"AQTLTrait:2252","label":"LDL cholesterol level"}]}},{"entity":"ClinVarVariant:159421","phenotype":{"types":[{"id":"HP:0100627","label":"Displacement of the external urethral meatus"}]}},{"entity":"MGI:2389580","phenotype":{"types":[{"id":"MP:0000952","label":"abnormal CNS glial cell morphology"}]}},{"entity":"ClinVarVariant:100651","phenotype":{"types":[{"id":"HP:0002553","label":"Highly arched eyebrow"}]}},{"entity":"FlyBase:FBal0277412","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:135775","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:189124","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:42053","phenotype":{"types":[{"id":"HP:0003281","label":"Increased serum ferritin"}]}},{"entity":"ClinVarVariant:18426","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:5965","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"ClinVarVariant:10867","phenotype":{"types":[{"id":"HP:0010972","label":"Anemia of inadequate production"}]}},{"entity":"ClinVarVariant:24410","phenotype":{"types":[{"id":"HP:0100633","label":"Esophagitis"}]}},{"entity":"AQTL:7240","phenotype":{"types":[{"id":"AQTLTrait:554","label":"Anal atresia"}]}},{"entity":"ClinVarVariant:97813","phenotype":{"types":[{"id":"HP:0001974","label":"Leukocytosis"}]}},{"entity":"ClinVarVariant:3642","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:49340","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"ClinVarVariant:24295","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"MGI:4849540","phenotype":{"types":[{"id":"MP:0009420","label":"skeletal muscle endomysial fibrosis"}]}},{"entity":"FlyBase:FBal0204839","phenotype":{"types":[{"id":"FBbt:00004729PHENOTYPE","label":"Drosophila wing phenotype"}]}},{"entity":"ClinVarVariant:96617","phenotype":{"types":[{"id":"HP:0006846","label":"Acute encephalopathy"}]}},{"entity":"ClinVarVariant:135766","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:38889","phenotype":{"types":[{"id":"HP:0002634","label":"Arteriosclerosis"}]}},{"entity":"MGI:1856150","phenotype":{"types":[{"id":"MP:0000159","label":"abnormal xiphoid process morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004887-WBRNAi00030287","phenotype":{"types":[{"id":"WBPhenotype:0000054","label":"larval lethal"}]}},{"entity":"ClinVarVariant:15282","phenotype":{"types":[{"id":"HP:0005505","label":"Refractory anemia"}]}},{"entity":"ClinVarVariant:21759","phenotype":{"types":[{"id":"HP:0002411","label":"Myokymia"}]}},{"entity":"AQTL:42663","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"ClinVarVariant:11445","phenotype":{"types":[{"id":"HP:0002136","label":"Broad-based gait"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001486-WBRNAi00102268","phenotype":{"types":[{"id":"WBPhenotype:0001900","label":"reduced levels of reduced glutathione"}]}},{"entity":"ClinVarVariant:194287","phenotype":{"types":[{"id":"HP:0004404","label":"Abnormality of the nipple"}]}},{"entity":"ClinVarVariant:167080","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:65853","phenotype":{"types":[{"id":"HP:0001274","label":"Agenesis of corpus callosum"}]}},{"entity":"ClinVarVariant:101152","phenotype":{"types":[{"id":"HP:0000490","label":"Deeply set eye"}]}},{"entity":"ClinVarVariant:180194","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"ClinVarVariant:60506","phenotype":{"types":[{"id":"HP:0003510","label":"Severe short stature"}]}},{"entity":"ClinVarVariant:159910","phenotype":{"types":[{"id":"HP:0003881","label":"Humeral sclerosis"}]}},{"entity":"FlyBase:FBal0244148","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:53229","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"AQTL:408","phenotype":{"types":[{"id":"AQTLTrait:2056","label":"Skin fat weight"}]}},{"entity":"NCBIGene:100302680","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"MGI:4429538","phenotype":{"types":[{"id":"MP:0008025","label":"brain vacuoles"}]}},{"entity":"ClinVarVariant:65014","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:162525","phenotype":{"types":[{"id":"HP:0008281","label":"Acute hyperammonemia"}]}},{"entity":"ClinVarVariant:157514","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001177-WBRNAi00061092","phenotype":{"types":[{"id":"WBPhenotype:0000279","label":"spicule insertion defective"}]}},{"entity":"FlyBase:FBal0258005","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:53758","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:53983","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:53422","phenotype":{"types":[{"id":"HP:0001948","label":"Alkalosis"}]}},{"entity":"FlyBase:FBal0042573","phenotype":{"types":[{"id":"FBbt:00000008PHENOTYPE","label":"Drosophila labral segment phenotype"}]}},{"entity":"ClinVarVariant:41171","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:188881","phenotype":{"types":[{"id":"HP:0001874","label":"Abnormality of neutrophils"}]}},{"entity":"ClinVarVariant:40291","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:7502","phenotype":{"types":[{"id":"HP:0007468","label":"Perifollicular hyperkeratosis"}]}},{"entity":"ClinVarVariant:7725","phenotype":{"types":[{"id":"HP:0007552","label":"Abnormal subcutaneous fat tissue distribution"}]}},{"entity":"ClinVarVariant:11577","phenotype":{"types":[{"id":"HP:0007018","label":"Attention deficit hyperactivity disorder"}]}},{"entity":"MGI:3771073","phenotype":{"types":[{"id":"MP:0003017","label":"decreased circulating bicarbonate level"}]}},{"entity":"ClinVarVariant:13335","phenotype":{"types":[{"id":"HP:0001644","label":"Dilated cardiomyopathy"}]}},{"entity":"ClinVarVariant:53336","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:49180","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:52318","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"MGI:1857270","phenotype":{"types":[{"id":"MP:0002655","label":"abnormal keratinocyte morphology"}]}},{"entity":"ClinVarVariant:161210","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:162038","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:31100","phenotype":{"types":[{"id":"HP:0002558","label":"Supernumerary nipple"}]}},{"entity":"ClinVarVariant:41098","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:167222","phenotype":{"types":[{"id":"HP:0002566","label":"Intestinal malrotation"}]}},{"entity":"ClinVarVariant:216765","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:10753","phenotype":{"types":[{"id":"HP:0012622","label":"Chronic kidney disease"}]}},{"entity":"ClinVarVariant:53982","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:184580","phenotype":{"types":[{"id":"HP:0100777","label":"Exostoses"}]}},{"entity":"ClinVarVariant:8986","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007704-WBRNAi00066087","phenotype":{"types":[{"id":"WBPhenotype:0000541","label":"cord commissures fail to reach target"}]}},{"entity":"MGI:2681122","phenotype":{"types":[{"id":"MP:0003868","label":"abnormal feces composition"}]}},{"entity":"dbSNP:rs6538140","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:53000","phenotype":{"types":[{"id":"HP:0000598","label":"Abnormality of the ear"}]}},{"entity":"ClinVarVariant:158819","phenotype":{"types":[{"id":"HP:0000340","label":"Sloping forehead"}]}},{"entity":"ClinVarVariant:15202","phenotype":{"types":[{"id":"HP:0008151","label":"Prolonged prothrombin time"}]}},{"entity":"MGI:2385836","phenotype":{"types":[{"id":"MP:0004087","label":"abnormal muscle fiber morphology"}]}},{"entity":"ClinVarVariant:3961","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:38352","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:8870","phenotype":{"types":[{"id":"HP:0001216","label":"Delayed ossification of carpal bones"}]}},{"entity":"ClinVarVariant:10053","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:49410","phenotype":{"types":[{"id":"HP:0002617","label":"Aneurysm"}]}},{"entity":"ClinVarVariant:49858","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"MGI:3838346","phenotype":{"types":[{"id":"MP:0003917","label":"increased kidney weight"}]}},{"entity":"MGI:2181194","phenotype":{"types":[{"id":"MP:0010970","label":"abnormal compact bone lamellar structure"}]}},{"entity":"ClinVarVariant:53813","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:6278","phenotype":{"types":[{"id":"HP:0011362","label":"Abnormal hair quantity"}]}},{"entity":"ClinVarVariant:24558","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"MGI:4843437","phenotype":{"types":[{"id":"MP:0010268","label":"decreased lymphoma incidence"}]}},{"entity":"ClinVarVariant:7993","phenotype":{"types":[{"id":"HP:0000912","label":"Sprengel anomaly"}]}},{"entity":"ClinVarVariant:11313","phenotype":{"types":[{"id":"HP:0003455","label":"Elevated long chain fatty acids"}]}},{"entity":"AQTL:13657","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"ClinVarVariant:66802","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:42315","phenotype":{"types":[{"id":"HP:0004933","label":"Ascending aortic dissection"}]}},{"entity":"ClinVarVariant:2827","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"ClinVarVariant:127449","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"MGI:3845884","phenotype":{"types":[{"id":"MP:0008019","label":"increased liver tumor incidence"}]}},{"entity":"ClinVarVariant:210769","phenotype":{"types":[{"id":"HP:0000336","label":"Prominent supraorbital ridges"}]}},{"entity":"ClinVarVariant:14051","phenotype":{"types":[{"id":"HP:0002359","label":"Frequent falls"}]}},{"entity":"ClinVarVariant:7224","phenotype":{"types":[{"id":"HP:0100651","label":"Type I diabetes mellitus"}]}},{"entity":"ClinVarVariant:196495","phenotype":{"types":[{"id":"HP:0002179","label":"Opisthotonus"}]}},{"entity":"ClinVarVariant:24621","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:201582","phenotype":{"types":[{"id":"HP:0100749","label":"Chest pain"}]}},{"entity":"ClinVarVariant:38322","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"MGI:1856691","phenotype":{"types":[{"id":"MP:0011101","label":"prenatal lethality, incomplete penetrance"}]}},{"entity":"ClinVarVariant:12207","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"ClinVarVariant:5028","phenotype":{"types":[{"id":"HP:0000230","label":"Gingivitis"}]}},{"entity":"MGI:3574072","phenotype":{"types":[{"id":"GO:0014037PHENOTYPE","label":"Schwann cell differentiation phenotype"}]}},{"entity":"FlyBase:FBal0206015","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:52308","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:53376","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:135892","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"AQTL:9532","phenotype":{"types":[{"id":"AQTLTrait:2029","label":"Tibia bone mineral content"}]}},{"entity":"ClinVarVariant:82771","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"ClinVarVariant:53264","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"FlyBase:FBal0218574","phenotype":{"types":[{"id":"FBbt:00004889PHENOTYPE","label":"karyosome phenotype"}]}},{"entity":"ClinVarVariant:35967","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"dbSNP:rs17135859","phenotype":{"types":[{"id":"HP:0002140","label":"Ischemic stroke"}]}},{"entity":"ClinVarVariant:159941","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"MGI:2181294","phenotype":{"types":[{"id":"MP:0009409","label":"abnormal skeletal muscle fiber type ratio"}]}},{"entity":"ClinVarVariant:211646","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"MGI:5056148","phenotype":{"types":[{"id":"MP:0001923","label":"reduced female fertility"}]}},{"entity":"ClinVarVariant:6711","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:163766","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ZFIN:ZDB-ALT-091112-20","phenotype":{"types":[{"id":"ZP:0001833","label":"abnormal(ly) deformed cranial cartilage"}]}},{"entity":"ClinVarVariant:39297","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"MGI:5441069","phenotype":{"types":[{"id":"MP:0004046","label":"abnormal mitosis"}]}},{"entity":"ClinVarVariant:24468","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:216732","phenotype":{"types":[{"id":"HP:0001541","label":"Ascites"}]}},{"entity":"FlyBase:FBal0316487","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"MGI:2183949","phenotype":{"types":[{"id":"MP:0003786","label":"premature aging"}]}},{"entity":"ClinVarVariant:41161","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:36567","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:24386","phenotype":{"types":[{"id":"HP:0008063","label":"Aplasia/Hypoplasia of the lens"}]}},{"entity":"AQTL:10182","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:158363","phenotype":{"types":[{"id":"HP:0000742","label":"Self-mutilation"}]}},{"entity":"ClinVarVariant:100721","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"MGI:3664305","phenotype":{"types":[{"id":"MP:0003137","label":"abnormal impulse conducting system conduction"}]}},{"entity":"ClinVarVariant:17282","phenotype":{"types":[{"id":"HP:0002273","label":"Tetraparesis"}]}},{"entity":"ClinVarVariant:159049","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:21789","phenotype":{"types":[{"id":"HP:0002411","label":"Myokymia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004726-WBRNAi00008634","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:4531","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:36309","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"ClinVarVariant:4367","phenotype":{"types":[{"id":"HP:0001776","label":"Bilateral talipes equinovarus"}]}},{"entity":"ClinVarVariant:67986","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:41142","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-030616-579-ZDB-MRPHLNO-070531-6","phenotype":{"types":[{"id":"GO:0031016PHENOTYPE","label":"pancreas development phenotype"}]}},{"entity":"ClinVarVariant:31224","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:199204","phenotype":{"types":[{"id":"HP:0002153","label":"Hyperkalemia"}]}},{"entity":"ClinVarVariant:13419","phenotype":{"types":[{"id":"HP:0002315","label":"Headache"}]}},{"entity":"ClinVarVariant:64785","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:198957","phenotype":{"types":[{"id":"HP:0010454","label":"Acetabular spurs"}]}},{"entity":"ClinVarVariant:6542","phenotype":{"types":[{"id":"HP:0007476","label":"Anhidrotic ectodermal dysplasia"}]}},{"entity":"ClinVarVariant:2648","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"FlyBase:FBal0051173","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:10766","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"AQTL:8854","phenotype":{"types":[{"id":"AQTLTrait:491","label":"Ear size"}]}},{"entity":"ClinVarVariant:136109","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:29986","phenotype":{"types":[{"id":"HP:0001376","label":"Limitation of joint mobility"}]}},{"entity":"ClinVarVariant:211645","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"ClinVarVariant:158349","phenotype":{"types":[{"id":"HP:0000343","label":"Long philtrum"}]}},{"entity":"ClinVarVariant:134889","phenotype":{"types":[{"id":"HP:0100634","label":"Neuroendocrine neoplasm"}]}},{"entity":"ClinVarVariant:10738","phenotype":{"types":[{"id":"HP:0100699","label":"Scarring"}]}},{"entity":"FlyBase:FBal0209081","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:190276","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"ClinVarVariant:14271","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:204288","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:155948","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:48922","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"ClinVarVariant:83179","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"ClinVarVariant:30382","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:204092","phenotype":{"types":[{"id":"HP:0009830","label":"Peripheral neuropathy"}]}},{"entity":"ClinVarVariant:13714","phenotype":{"types":[{"id":"HP:0002155","label":"Hypertriglyceridemia"}]}},{"entity":"ClinVarVariant:10130","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022792-WBRNAi00100525","phenotype":{"types":[{"id":"WBPhenotype:0000154","label":"reduced brood size"}]}},{"entity":"ClinVarVariant:38788","phenotype":{"types":[{"id":"HP:0011507","label":"Macular flecks"}]}},{"entity":"ClinVarVariant:16636","phenotype":{"types":[{"id":"HP:0007110","label":"Central hypoventilation"}]}},{"entity":"ClinVarVariant:215714","phenotype":{"types":[{"id":"HP:0002076","label":"Migraine"}]}},{"entity":"ClinVarVariant:92913","phenotype":{"types":[{"id":"HP:0100670","label":"Rough bone trabeculation"}]}},{"entity":"ClinVarVariant:142700","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:161996","phenotype":{"types":[{"id":"HP:0006538","label":"Recurrent bronchopulmonary infections"}]}},{"entity":"ClinVarVariant:162456","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:195849","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"AQTL:27763","phenotype":{"types":[{"id":"AQTLTrait:1485","label":"Mean corpuscular volume"}]}},{"entity":"ClinVarVariant:41168","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"AQTL:44243","phenotype":{"types":[{"id":"AQTLTrait:1136","label":"Bone quality"}]}},{"entity":"MGI:3772332","phenotype":{"types":[{"id":"MP:0000490","label":"abnormal crypts of Lieberkuhn morphology"}]}},{"entity":"ClinVarVariant:38414","phenotype":{"types":[{"id":"HP:0100790","label":"Hernia"}]}},{"entity":"ClinVarVariant:48957","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:65312","phenotype":{"types":[{"id":"HP:0000826","label":"Precocious puberty"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-060908-2-ZDB-MRPHLNO-100616-1","phenotype":{"types":[{"id":"ZP:0001349","label":"abnormal(ly) apoptotic eye"}]}},{"entity":"ClinVarVariant:5595","phenotype":{"types":[{"id":"HP:0002013","label":"Vomiting"}]}},{"entity":"AQTL:32791","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:160181","phenotype":{"types":[{"id":"HP:0001321","label":"Cerebellar hypoplasia"}]}},{"entity":"AQTL:53986","phenotype":{"types":[{"id":"AQTLTrait:1153","label":"Stillbirth"}]}},{"entity":"ClinVarVariant:10733","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"ClinVarVariant:49640","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:217079","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:97787","phenotype":{"types":[{"id":"HP:0100603","label":"Toxemia of pregnancy"}]}},{"entity":"ClinVarVariant:97554","phenotype":{"types":[{"id":"HP:0100769","label":"Synovitis"}]}},{"entity":"ClinVarVariant:11060","phenotype":{"types":[{"id":"HP:0002021","label":"Pyloric stenosis"}]}},{"entity":"ClinVarVariant:53357","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"ClinVarVariant:210443","phenotype":{"types":[{"id":"HP:0100545","label":"Arterial stenosis"}]}},{"entity":"MGI:4453204","phenotype":{"types":[{"id":"MP:0001922","label":"reduced male fertility"}]}},{"entity":"ClinVarVariant:35833","phenotype":{"types":[{"id":"HP:0001742","label":"Nasal obstruction"}]}},{"entity":"MGI:1856066","phenotype":{"types":[{"id":"HP:0011096","label":"Peripheral demyelination"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004919-WBRNAi00071373","phenotype":{"types":[{"id":"WBPhenotype:0000258","label":"cell secretion variant"}]}},{"entity":"ClinVarVariant:38626","phenotype":{"types":[{"id":"HP:0001578","label":"Hypercortisolism"}]}},{"entity":"ClinVarVariant:31676","phenotype":{"types":[{"id":"HP:0000448","label":"Prominent nose"}]}},{"entity":"MGI:3614434","phenotype":{"types":[{"id":"MP:0005536","label":"Leydig cell hypoplasia"}]}},{"entity":"ClinVarVariant:21358","phenotype":{"types":[{"id":"HP:0002553","label":"Highly arched eyebrow"}]}},{"entity":"ClinVarVariant:126095","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:3382","phenotype":{"types":[{"id":"HP:0006485","label":"Agenesis of incisor"}]}},{"entity":"ClinVarVariant:185554","phenotype":{"types":[{"id":"HP:0006721","label":"Acute lymphoblastic leukemia"}]}},{"entity":"FlyBase:FBal0135765","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"AQTL:6504","phenotype":{"types":[{"id":"AQTLTrait:2021","label":"Humerus length"}]}},{"entity":"ClinVarVariant:42385","phenotype":{"types":[{"id":"HP:0100719","label":"Lens coloboma"}]}},{"entity":"ClinVarVariant:53360","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:127117","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:25201","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"ClinVarVariant:189862","phenotype":{"types":[{"id":"HP:0002384","label":"Focal seizures with impairment of consciousness or awareness"}]}},{"entity":"ClinVarVariant:183683","phenotype":{"types":[{"id":"HP:0003164","label":"Hypothalamic gonadotropin-releasing hormone (GNRH) deficiency"}]}},{"entity":"ClinVarVariant:159370","phenotype":{"types":[{"id":"HP:0009890","label":"High anterior hairline"}]}},{"entity":"ClinVarVariant:216775","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"MGI:4364913","phenotype":{"types":[{"id":"MP:0006411","label":"upturned snout"}]}},{"entity":"MGI:1857852","phenotype":{"types":[{"id":"MP:0000872","label":"abnormal cerebellum external granule cell layer morphology"}]}},{"entity":"ClinVarVariant:215957","phenotype":{"types":[{"id":"HP:0005344","label":"Abnormality of the carotid arteries"}]}},{"entity":"MGI:3777145","phenotype":{"types":[{"id":"MP:0001981","label":"increased chemically-elicited antinociception"}]}},{"entity":"ClinVarVariant:65753","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:56716","phenotype":{"types":[{"id":"HP:0002074","label":"Increased neuronal autofluorescent lipopigment"}]}},{"entity":"ClinVarVariant:6643","phenotype":{"types":[{"id":"HP:0004944","label":"Cerebral aneurysm"}]}},{"entity":"ClinVarVariant:143406","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003920-WBRNAi00069781","phenotype":{"types":[{"id":"WBPhenotype:0000061","label":"extended life span"}]}},{"entity":"ClinVarVariant:7623","phenotype":{"types":[{"id":"HP:0001297","label":"Stroke"}]}},{"entity":"ZFIN:ZDB-ALT-040824-2","phenotype":{"types":[{"id":"ZP:0000961","label":"abnormal(ly) bent trunk"}]}},{"entity":"ClinVarVariant:35839","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:158283","phenotype":{"types":[{"id":"HP:0001888","label":"Lymphopenia"}]}},{"entity":"AQTL:31062","phenotype":{"types":[{"id":"AQTLTrait:1169","label":"Interval to first estrus after calving"}]}},{"entity":"ClinVarVariant:11454","phenotype":{"types":[{"id":"HP:0000971","label":"Abnormality of the sweat gland"}]}},{"entity":"ClinVarVariant:17349","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"MGI:1927183","phenotype":{"types":[{"id":"MP:0008571","label":"abnormal synaptic bouton morphology"}]}},{"entity":"ClinVarVariant:211736","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:54175","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:132825","phenotype":{"types":[{"id":"HP:0002140","label":"Ischemic stroke"}]}},{"entity":"MGI:3620102","phenotype":{"types":[{"id":"MP:0003887","label":"increased hepatocyte apoptosis"}]}},{"entity":"MGI:2450309","phenotype":{"types":[{"id":"MP:0000260","label":"abnormal angiogenesis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001691-WBRNAi00076971","phenotype":{"types":[{"id":"WBPhenotype:0000280","label":"breaks in alae"}]}},{"entity":"ClinVarVariant:97923","phenotype":{"types":[{"id":"HP:0001917","label":"Renal amyloidosis"}]}},{"entity":"FlyBase:FBal0138238","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:88857","phenotype":{"types":[{"id":"HP:0000787","label":"Nephrolithiasis"}]}},{"entity":"ClinVarVariant:788","phenotype":{"types":[{"id":"HP:0001640","label":"Cardiomegaly"}]}},{"entity":"ClinVarVariant:11901","phenotype":{"types":[{"id":"HP:0008169","label":"Reduced factor VII activity"}]}},{"entity":"MGI:2388055","phenotype":{"types":[{"id":"MP:0005325","label":"abnormal renal glomerulus morphology"}]}},{"entity":"ClinVarVariant:30944","phenotype":{"types":[{"id":"HP:0003026","label":"Short long bone"}]}},{"entity":"ClinVarVariant:1483","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:1369","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:41065","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:10108","phenotype":{"types":[{"id":"HP:0100726","label":"Kaposi's sarcoma"}]}},{"entity":"ClinVarVariant:10757","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"ClinVarVariant:210471","phenotype":{"types":[{"id":"HP:0002208","label":"Coarse hair"}]}},{"entity":"AQTL:12523","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"dbSNP:rs12294076","phenotype":{"types":[{"id":"HP:0000211","label":"Trismus"}]}},{"entity":"ClinVarVariant:4221","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:159447","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"MGI:4432654","phenotype":{"types":[{"id":"MP:0003131","label":"increased erythrocyte cell number"}]}},{"entity":"ClinVarVariant:216216","phenotype":{"types":[{"id":"HP:0003254","label":"Abnormality of DNA repair"}]}},{"entity":"ClinVarVariant:42397","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"MGI:1933764","phenotype":{"types":[{"id":"MP:0000814","label":"absent dentate gyrus"}]}},{"entity":"ClinVarVariant:5487","phenotype":{"types":[{"id":"HP:0011958","label":"Retinal perforation"}]}},{"entity":"ClinVarVariant:158894","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:10987","phenotype":{"types":[{"id":"HP:0003217","label":"Hyperglutaminemia"}]}},{"entity":"ClinVarVariant:53294","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:10124","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:30491","phenotype":{"types":[{"id":"HP:0003765","label":"Psoriasis"}]}},{"entity":"ClinVarVariant:189593","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:68497","phenotype":{"types":[{"id":"HP:0001047","label":"Atopic dermatitis"}]}},{"entity":"ClinVarVariant:210028","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:9922","phenotype":{"types":[{"id":"HP:0010529","label":"Echolalia"}]}},{"entity":"ClinVarVariant:42017","phenotype":{"types":[{"id":"HP:0000951","label":"Abnormality of the skin"}]}},{"entity":"ClinVarVariant:35887","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"ClinVarVariant:143254","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"ZFIN:ZDB-ALT-121210-2","phenotype":{"types":[{"id":"ZP:0012714","label":"abnormal(ly) mislocalised pancreas neutrophil"}]}},{"entity":"ClinVarVariant:53973","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:99926","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:39637","phenotype":{"types":[{"id":"HP:0000405","label":"Conductive hearing impairment"}]}},{"entity":"ClinVarVariant:30547","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ClinVarVariant:36051","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:11592","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"ClinVarVariant:4301","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:42066","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:41149","phenotype":{"types":[{"id":"HP:0000668","label":"Hypodontia"}]}},{"entity":"MGI:1856601","phenotype":{"types":[{"id":"MP:0009474","label":"thick epidermis stratum spinosum"}]}},{"entity":"ClinVarVariant:38306","phenotype":{"types":[{"id":"HP:0008551","label":"Microtia"}]}},{"entity":"ClinVarVariant:1957","phenotype":{"types":[{"id":"HP:0002644","label":"Abnormality of pelvic girdle bone morphology"}]}},{"entity":"ClinVarVariant:24677","phenotype":{"types":[{"id":"HP:0100633","label":"Esophagitis"}]}},{"entity":"ClinVarVariant:179546","phenotype":{"types":[{"id":"HP:0002017","label":"Nausea and vomiting"}]}},{"entity":"ClinVarVariant:189086","phenotype":{"types":[{"id":"HP:0000400","label":"Macrotia"}]}},{"entity":"ClinVarVariant:1450","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"MGI:5513765","phenotype":{"types":[{"id":"MP:0005635","label":"decreased circulating bilirubin level"}]}},{"entity":"ClinVarVariant:53628","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:126974","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:199200","phenotype":{"types":[{"id":"HP:0012043","label":"Pendular nystagmus"}]}},{"entity":"ClinVarVariant:53703","phenotype":{"types":[{"id":"HP:0100660","label":"Dyskinesia"}]}},{"entity":"MGI:3695897","phenotype":{"types":[{"id":"MP:0000755","label":"hindlimb paralysis"}]}},{"entity":"MGI:3040330","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"ClinVarVariant:7165","phenotype":{"types":[{"id":"HP:0001081","label":"Cholelithiasis"}]}},{"entity":"ClinVarVariant:5894","phenotype":{"types":[{"id":"HP:0000509","label":"Conjunctivitis"}]}},{"entity":"AQTL:26651","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:9617","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"FlyBase:FBal0261159","phenotype":{"types":[{"id":"FBcv:0000399","label":"courtship behavior defective"}]}},{"entity":"ClinVarVariant:159204","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:211653","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"MGI:2677447","phenotype":{"types":[{"id":"MP:0001825","label":"arrested T cell differentiation"}]}},{"entity":"ClinVarVariant:210388","phenotype":{"types":[{"id":"HP:0005054","label":"Metaphyseal spurs"}]}},{"entity":"ClinVarVariant:49421","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"ClinVarVariant:6459","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:5082","phenotype":{"types":[{"id":"HP:0003557","label":"Increased variability in muscle fiber diameter"}]}},{"entity":"ClinVarVariant:6582","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"ClinVarVariant:8884","phenotype":{"types":[{"id":"HP:0000567","label":"Chorioretinal coloboma"}]}},{"entity":"MGI:2179545","phenotype":{"types":[{"id":"MP:0002123","label":"abnormal definitive hematopoiesis"}]}},{"entity":"ClinVarVariant:53369","phenotype":{"types":[{"id":"HP:0000855","label":"Insulin resistance"}]}},{"entity":"MGI:2180680","phenotype":{"types":[{"id":"MP:0008188","label":"abnormal transitional stage B cell morphology"}]}},{"entity":"FlyBase:FBal0304813","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:49575","phenotype":{"types":[{"id":"HP:0009716","label":"Subependymal nodules"}]}},{"entity":"ClinVarVariant:1018","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:48862","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"MGI:2662305","phenotype":{"types":[{"id":"MP:0001622","label":"abnormal vasculogenesis"}]}},{"entity":"ClinVarVariant:39056","phenotype":{"types":[{"id":"HP:0003026","label":"Short long bone"}]}},{"entity":"ClinVarVariant:10743","phenotype":{"types":[{"id":"HP:0009763","label":"Limb pain"}]}},{"entity":"ClinVarVariant:44203","phenotype":{"types":[{"id":"HP:0007411","label":"Hypoplastic-absent sebaceous glands"}]}},{"entity":"MGI:1857291","phenotype":{"types":[{"id":"MP:0000628","label":"abnormal mammary gland development"}]}},{"entity":"ClinVarVariant:158724","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"MGI:2149065","phenotype":{"types":[{"id":"MP:0001900","label":"impaired synaptic plasticity"}]}},{"entity":"ClinVarVariant:97611","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"MGI:2176201","phenotype":{"types":[{"id":"MP:0003566","label":"abnormal cell adhesion"}]}},{"entity":"ClinVarVariant:24806","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ClinVarVariant:158359","phenotype":{"types":[{"id":"HP:0009765","label":"Low hanging columella"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003918-WBRNAi00083243","phenotype":{"types":[{"id":"WBPhenotype:0000425","label":"antibody staining reduced"}]}},{"entity":"ClinVarVariant:68536","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"FlyBase:FBal0059988","phenotype":{"types":[{"id":"FBbt:00004218PHENOTYPE","label":"Drosophila rhabdomere R3 phenotype"}]}},{"entity":"ClinVarVariant:53220","phenotype":{"types":[{"id":"HP:0006536","label":"Obstructive lung disease"}]}},{"entity":"ClinVarVariant:11550","phenotype":{"types":[{"id":"HP:0002747","label":"Respiratory insufficiency due to muscle weakness"}]}},{"entity":"WormBase:WBVar00252908","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:156338","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:31196","phenotype":{"types":[{"id":"HP:0003128","label":"Lactic acidosis"}]}},{"entity":"ClinVarVariant:10709","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"ClinVarVariant:65353","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:38749","phenotype":{"types":[{"id":"HP:0005101","label":"High-frequency hearing impairment"}]}},{"entity":"ClinVarVariant:53801","phenotype":{"types":[{"id":"HP:0006538","label":"Recurrent bronchopulmonary infections"}]}},{"entity":"ClinVarVariant:5561","phenotype":{"types":[{"id":"HP:0005227","label":"Adenomatous colonic polyposis"}]}},{"entity":"ClinVarVariant:136110","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:156138","phenotype":{"types":[{"id":"HP:0001319","label":"Neonatal hypotonia"}]}},{"entity":"ClinVarVariant:120246","phenotype":{"types":[{"id":"HP:0002162","label":"Low posterior hairline"}]}},{"entity":"ClinVarVariant:196277","phenotype":{"types":[{"id":"HP:0006510","label":"Chronic obstructive pulmonary disease"}]}},{"entity":"FlyBase:FBal0207442","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"dbSNP:rs41946434","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"MGI:2176172","phenotype":{"types":[{"id":"MP:0000876","label":"Purkinje cell degeneration"}]}},{"entity":"dbSNP:rs43488797","phenotype":{"types":[{"id":"AQTLTrait:1120","label":"Thurl width"}]}},{"entity":"ClinVarVariant:65533","phenotype":{"types":[{"id":"HP:0004432","label":"Agammaglobulinemia"}]}},{"entity":"ClinVarVariant:7706","phenotype":{"types":[{"id":"HP:0000114","label":"Proximal tubulopathy"}]}},{"entity":"ClinVarVariant:135896","phenotype":{"types":[{"id":"HP:0009733","label":"Glioma"}]}},{"entity":"ClinVarVariant:38975","phenotype":{"types":[{"id":"HP:0003236","label":"Elevated serum creatine phosphokinase"}]}},{"entity":"ClinVarVariant:1967","phenotype":{"types":[{"id":"HP:0002644","label":"Abnormality of pelvic girdle bone morphology"}]}},{"entity":"ClinVarVariant:127165","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:189084","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:1173","phenotype":{"types":[{"id":"HP:0008726","label":"Hypoplasia of the vagina"}]}},{"entity":"ClinVarVariant:15413","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"dbSNP:rs81307772","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"NCBIGene:100462676","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"AQTL:44219","phenotype":{"types":[{"id":"AQTLTrait:1173","label":"Rear leg set"}]}},{"entity":"FlyBase:FBal0284419","phenotype":{"types":[{"id":"FBbt:00003625PHENOTYPE","label":"Drosophila adult brain cell body rind phenotype"}]}},{"entity":"dbSNP:rs110474527","phenotype":{"types":[{"id":"AQTLTrait:1070","label":"Inseminations per conception"}]}},{"entity":"ClinVarVariant:13325","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:156338","phenotype":{"types":[{"id":"HP:0002863","label":"Myelodysplasia"}]}},{"entity":"ClinVarVariant:53718","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:208015","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"FlyBase:FBal0201465","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:41102","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:101364","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:35456","phenotype":{"types":[{"id":"HP:0002097","label":"Emphysema"}]}},{"entity":"WormBase:WBVar00087959","phenotype":{"types":[{"id":"WBPhenotype:0001645","label":"protein degradation variant"}]}},{"entity":"ClinVarVariant:120266","phenotype":{"types":[{"id":"HP:0001010","label":"Hypopigmentation of the skin"}]}},{"entity":"FlyBase:FBal0210406","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:10315","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:53332","phenotype":{"types":[{"id":"HP:0100889","label":"Abnormality of the ductus choledochus"}]}},{"entity":"ClinVarVariant:210467","phenotype":{"types":[{"id":"HP:0008070","label":"Sparse hair"}]}},{"entity":"ClinVarVariant:101212","phenotype":{"types":[{"id":"HP:0005267","label":"Premature delivery because of cervical insufficiency or membrane fragility"}]}},{"entity":"ClinVarVariant:24816","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ZFIN:ZDB-ALT-040716-2","phenotype":{"types":[{"id":"ZP:0006289","label":"abnormal(ly) detached from goblet cell towards intestinal epithelium"}]}},{"entity":"ClinVarVariant:65876","phenotype":{"types":[{"id":"HP:0009824","label":"Upper limb undergrowth"}]}},{"entity":"ClinVarVariant:24437","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"FlyBase:FBal0182631","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:53907","phenotype":{"types":[{"id":"HP:0005232","label":"Pancreatic dysplasia"}]}},{"entity":"FlyBase:FBal0211026","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:92734","phenotype":{"types":[{"id":"HP:0100324","label":"Scleroderma"}]}},{"entity":"ClinVarVariant:209982","phenotype":{"types":[{"id":"HP:0003487","label":"Babinski sign"}]}},{"entity":"ClinVarVariant:126869","phenotype":{"types":[{"id":"HP:0004724","label":"Calcium nephrolithiasis"}]}},{"entity":"ClinVarVariant:101374","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:42515","phenotype":{"types":[{"id":"HP:0000859","label":"Hyperaldosteronism"}]}},{"entity":"ClinVarVariant:188150","phenotype":{"types":[{"id":"HP:0009650","label":"Short distal phalanx of the thumb"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00044068-WBRNAi00075201","phenotype":{"types":[{"id":"WBPhenotype:0000154","label":"reduced brood size"}]}},{"entity":"ClinVarVariant:10457","phenotype":{"types":[{"id":"HP:0007763","label":"Retinal telangiectasia"}]}},{"entity":"ZFIN:ZDB-ALT-151110-1","phenotype":{"types":[{"id":"ZP:0002010","label":"abnormal(ly) morphology pancreas"}]}},{"entity":"FlyBase:FBal0208456","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:97422","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:7963","phenotype":{"types":[{"id":"HP:0010808","label":"Protruding tongue"}]}},{"entity":"ClinVarVariant:159677","phenotype":{"types":[{"id":"HP:0000368","label":"Low-set, posteriorly rotated ears"}]}},{"entity":"ClinVarVariant:21275","phenotype":{"types":[{"id":"HP:0011069","label":"Increased number of teeth"}]}},{"entity":"ClinVarVariant:39124","phenotype":{"types":[{"id":"HP:0006510","label":"Chronic obstructive pulmonary disease"}]}},{"entity":"ClinVarVariant:24454","phenotype":{"types":[{"id":"HP:0007763","label":"Retinal telangiectasia"}]}},{"entity":"MGI:3513254","phenotype":{"types":[{"id":"GO:0001756PHENOTYPE","label":"somitogenesis phenotype"}]}},{"entity":"ClinVarVariant:208427","phenotype":{"types":[{"id":"HP:0000926","label":"Platyspondyly"}]}},{"entity":"ClinVarVariant:3365","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:160227","phenotype":{"types":[{"id":"HP:0002070","label":"Limb ataxia"}]}},{"entity":"ClinVarVariant:53941","phenotype":{"types":[{"id":"HP:0003453","label":"Antineutrophil antibody positivity"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003020-WBRNAi00075368","phenotype":{"types":[{"id":"WBPhenotype:0000700","label":"multivulva"}]}},{"entity":"ClinVarVariant:161234","phenotype":{"types":[{"id":"HP:0007906","label":"Increased intraocular pressure"}]}},{"entity":"ClinVarVariant:217039","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"AQTL:23159","phenotype":{"types":[{"id":"AQTLTrait:2061","label":"Wing weight"}]}},{"entity":"MGI:3716711","phenotype":{"types":[{"id":"HP:0040189","label":"Scaling skin"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001832-WBRNAi00005000","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"WormBase:WBVar00087794","phenotype":{"types":[{"id":"WBPhenotype:0001683","label":"spermatogenesis defective hermaphrodite"}]}},{"entity":"AQTL:17561","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:11816","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:35572","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:211143","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"MGI:2180013","phenotype":{"types":[{"id":"MP:0001119","label":"abnormal female reproductive system morphology"}]}},{"entity":"FlyBase:FBal0296773","phenotype":{"types":[{"id":"FBbt:00004729PHENOTYPE","label":"Drosophila wing phenotype"}]}},{"entity":"ClinVarVariant:54008","phenotype":{"types":[{"id":"HP:0011850","label":"Parotitis"}]}},{"entity":"ClinVarVariant:183671","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"MGI:3615021","phenotype":{"types":[{"id":"HP:0004447","label":"Poikilocytosis"}]}},{"entity":"ClinVarVariant:18370","phenotype":{"types":[{"id":"HP:0000343","label":"Long philtrum"}]}},{"entity":"MGI:2429312","phenotype":{"types":[{"id":"MP:0006404","label":"abnormal lumbar dorsal root ganglion morphology"}]}},{"entity":"ClinVarVariant:10859","phenotype":{"types":[{"id":"HP:0010299","label":"Abnormality of dentin"}]}},{"entity":"ClinVarVariant:101185","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:3866","phenotype":{"types":[{"id":"HP:0002275","label":"Poor motor coordination"}]}},{"entity":"ClinVarVariant:42377","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"ClinVarVariant:55944","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:10728","phenotype":{"types":[{"id":"HP:0000763","label":"Sensory neuropathy"}]}},{"entity":"dbSNP:rs109894613","phenotype":{"types":[{"id":"AQTLTrait:1115","label":"Chest width"}]}},{"entity":"ClinVarVariant:92621","phenotype":{"types":[{"id":"HP:0003541","label":"Urinary glycosaminoglycan excretion"}]}},{"entity":"ClinVarVariant:31028","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"ZFIN:ZDB-ALT-090702-3","phenotype":{"types":[{"id":"ZP:0015766","label":"abnormal(ly) black mouth melanoma"}]}},{"entity":"ClinVarVariant:11734","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"FlyBase:FBal0194748","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:100637","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:135758","phenotype":{"types":[{"id":"HP:0008348","label":"Immunoglobulin IgG2 deficiency"}]}},{"entity":"ClinVarVariant:38922","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:10582","phenotype":{"types":[{"id":"HP:0005186","label":"Synovial hypertrophy"}]}},{"entity":"ClinVarVariant:216388","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:24677","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"MGI:3665249","phenotype":{"types":[{"id":"MP:0013744","label":"abnormal conjunctival sac morphology"}]}},{"entity":"ClinVarVariant:2715","phenotype":{"types":[{"id":"HP:0000992","label":"Cutaneous photosensitivity"}]}},{"entity":"ClinVarVariant:25244","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:161456","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:7165","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:10229","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:216144","phenotype":{"types":[{"id":"HP:0000090","label":"Nephronophthisis"}]}},{"entity":"MGI:3837303","phenotype":{"types":[{"id":"HP:0011116","label":"Abnormality of interferon secretion"}]}},{"entity":"ClinVarVariant:1460","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:56659","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004357-WBRNAi00085604","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:24792","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:135759","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"MGI:2682796","phenotype":{"types":[{"id":"MP:0003156","label":"abnormal leukocyte migration"}]}},{"entity":"ClinVarVariant:5946","phenotype":{"types":[{"id":"HP:0001260","label":"Dysarthria"}]}},{"entity":"ClinVarVariant:159201","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:49536","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:7401","phenotype":{"types":[{"id":"HP:0001100","label":"Heterochromia iridis"}]}},{"entity":"FlyBase:FBal0264413","phenotype":{"types":[{"id":"FBbt:00001896PHENOTYPE","label":"Drosophila embryonic/larval Malpighian tubule phenotype"}]}},{"entity":"ClinVarVariant:1049","phenotype":{"types":[{"id":"HP:0000682","label":"Abnormality of dental enamel"}]}},{"entity":"ClinVarVariant:67861","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"MGI:4288793","phenotype":{"types":[{"id":"HP:0000137","label":"Abnormality of the ovary"}]}},{"entity":"FlyBase:FBal0199496","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:53723","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"FlyBase:FBal0209583","phenotype":{"types":[{"id":"FBbt:00004580PHENOTYPE","label":"Drosophila mesothoracic tergum phenotype"}]}},{"entity":"ClinVarVariant:44810","phenotype":{"types":[{"id":"HP:0000465","label":"Webbed neck"}]}},{"entity":"ClinVarVariant:15485","phenotype":{"types":[{"id":"HP:0000786","label":"Primary amenorrhea"}]}},{"entity":"ClinVarVariant:216565","phenotype":{"types":[{"id":"HP:0005403","label":"T lymphocytopenia"}]}},{"entity":"ClinVarVariant:91690","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:92324","phenotype":{"types":[{"id":"HP:0000726","label":"Dementia"}]}},{"entity":"ClinVarVariant:24458","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"dbSNP:rs1075309","phenotype":{"types":[{"id":"HP:0011134","label":"Low-grade fever"}]}},{"entity":"ClinVarVariant:165011","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:8836","phenotype":{"types":[{"id":"HP:0011036","label":"Abnormality of renal excretion"}]}},{"entity":"ClinVarVariant:96439","phenotype":{"types":[{"id":"HP:0000457","label":"Depressed nasal ridge"}]}},{"entity":"ClinVarVariant:210712","phenotype":{"types":[{"id":"HP:0008572","label":"External ear malformation"}]}},{"entity":"ClinVarVariant:187907","phenotype":{"types":[{"id":"HP:0100786","label":"Hypersomnia"}]}},{"entity":"ClinVarVariant:53514","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"ClinVarVariant:159161","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"FlyBase:FBal0230433","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:35716","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:16678","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:10731","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:53667","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:211663","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"ClinVarVariant:5779","phenotype":{"types":[{"id":"HP:0000722","label":"Obsessive-compulsive behavior"}]}},{"entity":"ClinVarVariant:97644","phenotype":{"types":[{"id":"HP:0100539","label":"Periorbital edema"}]}},{"entity":"ClinVarVariant:159206","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:53393","phenotype":{"types":[{"id":"HP:0006706","label":"Cystic liver disease"}]}},{"entity":"ClinVarVariant:83176","phenotype":{"types":[{"id":"HP:0006740","label":"Transitional cell carcinoma of the bladder"}]}},{"entity":"ClinVarVariant:48917","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:216392","phenotype":{"types":[{"id":"HP:0001012","label":"Multiple lipomas"}]}},{"entity":"ClinVarVariant:161976","phenotype":{"types":[{"id":"HP:0001269","label":"Hemiparesis"}]}},{"entity":"ClinVarVariant:16993","phenotype":{"types":[{"id":"HP:0000691","label":"Microdontia"}]}},{"entity":"FlyBase:FBal0059537","phenotype":{"types":[{"id":"FBbt:00001730PHENOTYPE","label":"Drosophila larval head phenotype"}]}},{"entity":"ClinVarVariant:36475","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:159214","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:7155","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:11662","phenotype":{"types":[{"id":"HP:0000687","label":"Widely spaced teeth"}]}},{"entity":"ClinVarVariant:12002","phenotype":{"types":[{"id":"HP:0010980","label":"Hyperlipoproteinemia"}]}},{"entity":"NCBIGene:1913","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"ZFIN:ZDB-ALT-100409-2","phenotype":{"types":[{"id":"ZP:0016420","label":"abnormal(ly) has extra parts of type integument towards cell"}]}},{"entity":"ClinVarVariant:53894","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:167228","phenotype":{"types":[{"id":"HP:0000592","label":"Blue sclerae"}]}},{"entity":"ClinVarVariant:9429","phenotype":{"types":[{"id":"HP:0000632","label":"Lacrimation abnormality"}]}},{"entity":"dbSNP:rs6676375","phenotype":{"types":[{"id":"HP:0001254","label":"Lethargy"}]}},{"entity":"ClinVarVariant:100787","phenotype":{"types":[{"id":"HP:0009803","label":"Short phalanx of finger"}]}},{"entity":"ClinVarVariant:41422","phenotype":{"types":[{"id":"HP:0005855","label":"Multiple prenatal fractures"}]}},{"entity":"ZFIN:ZDB-ALT-070531-2","phenotype":{"types":[{"id":"ZP:0008366","label":"abnormal(ly) having decreased processual parts liver development towards cell proliferation"}]}},{"entity":"ClinVarVariant:97671","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"MGI:3814908","phenotype":{"types":[{"id":"HP:0010976","label":"B lymphocytopenia"}]}},{"entity":"ClinVarVariant:183069","phenotype":{"types":[{"id":"HP:0008256","label":"Adrenocortical adenoma"}]}},{"entity":"ClinVarVariant:56778","phenotype":{"types":[{"id":"HP:0002084","label":"Encephalocele"}]}},{"entity":"dbSNP:rs41697837","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:2588","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:184381","phenotype":{"types":[{"id":"HP:0002897","label":"Parathyroid adenoma"}]}},{"entity":"ClinVarVariant:135896","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"MGI:1857077","phenotype":{"types":[{"id":"MP:0013173","label":"trigeminal ganglion degeneration"}]}},{"entity":"ClinVarVariant:158776","phenotype":{"types":[{"id":"HP:0000826","label":"Precocious puberty"}]}},{"entity":"ClinVarVariant:1704","phenotype":{"types":[{"id":"HP:0003481","label":"Segmental peripheral demyelination/remyelination"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1302","phenotype":{"types":[{"id":"ZP:0000766","label":"abnormal(ly) bent post-vent region"}]}},{"entity":"ClinVarVariant:200395","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:126966","phenotype":{"types":[{"id":"HP:0001402","label":"Hepatocellular carcinoma"}]}},{"entity":"ClinVarVariant:1633","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"FlyBase:FBal0091132","phenotype":{"types":[{"id":"FBcv:0002027","label":"lethal - all die before end of pupal stage"}]}},{"entity":"ClinVarVariant:48892","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"ClinVarVariant:36061","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:5923","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"MGI:3826836","phenotype":{"types":[{"id":"MP:0009431","label":"decreased fetal weight"}]}},{"entity":"dbSNP:rs11886868","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:159683","phenotype":{"types":[{"id":"HP:0006461","label":"Proximal femoral epiphysiolysis"}]}},{"entity":"MGI:3762641","phenotype":{"types":[{"id":"MP:0011089","label":"perinatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:5545","phenotype":{"types":[{"id":"HP:0000972","label":"Palmoplantar hyperkeratosis"}]}},{"entity":"ClinVarVariant:13344","phenotype":{"types":[{"id":"HP:0000506","label":"Telecanthus"}]}},{"entity":"ClinVarVariant:3988","phenotype":{"types":[{"id":"HP:0006829","label":"Severe muscular hypotonia"}]}},{"entity":"ClinVarVariant:143170","phenotype":{"types":[{"id":"HP:0003474","label":"Sensory impairment"}]}},{"entity":"ClinVarVariant:49708","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:64689","phenotype":{"types":[{"id":"HP:0000445","label":"Wide nose"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006528-WBRNAi00085576","phenotype":{"types":[{"id":"WBPhenotype:0001982","label":"cell membrane organization biogenesis variant"}]}},{"entity":"ClinVarVariant:571","phenotype":{"types":[{"id":"HP:0000618","label":"Blindness"}]}},{"entity":"OMIM:226000","phenotype":{"types":[{"id":"HP:0001711","label":"Abnormality of the left ventricle"}]}},{"entity":"ClinVarVariant:209137","phenotype":{"types":[{"id":"HP:0001673","label":"Tachycardia (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:49501","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:7175","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:210451","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"MGI:3800176","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:120276","phenotype":{"types":[{"id":"HP:0001010","label":"Hypopigmentation of the skin"}]}},{"entity":"ClinVarVariant:24361","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"MGI:3527937","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:216466","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000065-WBRNAi00026399","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"AQTL:40844","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:10887","phenotype":{"types":[{"id":"HP:0002872","label":"Apneic episodes precipitated by illness, fatigue, stress"}]}},{"entity":"ClinVarVariant:10737","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001973-WBRNAi00063017","phenotype":{"types":[{"id":"WBPhenotype:0000709","label":"pharyngeal morphology variant"}]}},{"entity":"ClinVarVariant:3360","phenotype":{"types":[{"id":"HP:0009926","label":"Increased lacrimation"}]}},{"entity":"ClinVarVariant:54089","phenotype":{"types":[{"id":"HP:0001622","label":"Premature birth"}]}},{"entity":"FlyBase:FBal0051201","phenotype":{"types":[{"id":"FBbt:00003921PHENOTYPE","label":"optic chiasma phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000415-WBRNAi00097824","phenotype":{"types":[{"id":"WBPhenotype:0000243","label":"engulfment failure by killer cell"}]}},{"entity":"ClinVarVariant:56788","phenotype":{"types":[{"id":"HP:0002084","label":"Encephalocele"}]}},{"entity":"ClinVarVariant:35859","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:68302","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:209028","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"ClinVarVariant:18331","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:50912","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:634","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:53929","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ClinVarVariant:4330","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"ClinVarVariant:17521","phenotype":{"types":[{"id":"HP:0000127","label":"Renal salt wasting"}]}},{"entity":"MGI:3818518","phenotype":{"types":[{"id":"MP:0004179","label":"transmission ratio distortion"}]}},{"entity":"ClinVarVariant:3097","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"ClinVarVariant:14793","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:24745","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:215969","phenotype":{"types":[{"id":"HP:0007707","label":"Congenital primary aphakia"}]}},{"entity":"ClinVarVariant:12401","phenotype":{"types":[{"id":"HP:0002290","label":"Poliosis"}]}},{"entity":"FlyBase:FBal0199313","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"MGI:5086003","phenotype":{"types":[{"id":"MP:0010875","label":"increased bone volume"}]}},{"entity":"MGI:3707421","phenotype":{"types":[{"id":"MP:0003088","label":"abnormal prepulse inhibition"}]}},{"entity":"ClinVarVariant:55954","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:97691","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"NCBIGene:171","phenotype":{"types":[{"id":"HP:0001199","label":"Triphalangeal thumb"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004978-WBRNAi00084613","phenotype":{"types":[{"id":"WBPhenotype:0001719","label":"unfolded protein response variant"}]}},{"entity":"ClinVarVariant:143524","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"ClinVarVariant:3678","phenotype":{"types":[{"id":"HP:0002194","label":"Delayed gross motor development"}]}},{"entity":"FlyBase:FBal0040484","phenotype":{"types":[{"id":"FBbt:00001761PHENOTYPE","label":"Drosophila imaginal disc phenotype"}]}},{"entity":"ClinVarVariant:10176","phenotype":{"types":[{"id":"HP:0005268","label":"Spontaneous abortion"}]}},{"entity":"ClinVarVariant:49511","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:54082","phenotype":{"types":[{"id":"HP:0012236","label":"Elevated sweat chloride"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00021351-WBRNAi00080537","phenotype":{"types":[{"id":"WBPhenotype:0000154","label":"reduced brood size"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002324-WBRNAi00000137","phenotype":{"types":[{"id":"WBPhenotype:0000038","label":"exploded through vulva"}]}},{"entity":"MGI:1926955","phenotype":{"types":[{"id":"HP:0001067","label":"Neurofibromas"}]}},{"entity":"ClinVarVariant:101404","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:180631","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"ClinVarVariant:66441","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"ClinVarVariant:2241","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"FlyBase:FBal0062864","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:1730","phenotype":{"types":[{"id":"HP:0007503","label":"Generalized ichthyosis"}]}},{"entity":"ClinVarVariant:82791","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"ClinVarVariant:30189","phenotype":{"types":[{"id":"HP:0000845","label":"Growth hormone excess"}]}},{"entity":"ClinVarVariant:558","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:6718","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"MGI:2674242","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"MGI:3757609","phenotype":{"types":[{"id":"MP:0003107","label":"abnormal response to novelty"}]}},{"entity":"ClinVarVariant:7394","phenotype":{"types":[{"id":"HP:0002226","label":"White eyebrow"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003048-WBRNAi00062630","phenotype":{"types":[{"id":"WBPhenotype:0001102","label":"mitotic spindle defective early emb"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-061110-61-ZDB-MRPHLNO-120409-1","phenotype":{"types":[{"id":"ZP:0002202","label":"abnormal(ly) edematous whole organism"}]}},{"entity":"ClinVarVariant:3622","phenotype":{"types":[{"id":"HP:0007819","label":"Presenile cataracts"}]}},{"entity":"ClinVarVariant:188235","phenotype":{"types":[{"id":"HP:0100699","label":"Scarring"}]}},{"entity":"ClinVarVariant:40502","phenotype":{"types":[{"id":"HP:0000276","label":"Long face"}]}},{"entity":"ZFIN:ZDB-ALT-040723-8","phenotype":{"types":[{"id":"ZP:0002256","label":"abnormal(ly) distended fourth ventricle"}]}},{"entity":"FlyBase:FBal0143183","phenotype":{"types":[{"id":"FBbt:00004729PHENOTYPE","label":"Drosophila wing phenotype"}]}},{"entity":"ClinVarVariant:11657","phenotype":{"types":[{"id":"HP:0001187","label":"Hyperextensibility of the finger joints"}]}},{"entity":"ClinVarVariant:5462","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"MGI:4431999","phenotype":{"types":[{"id":"HP:0003228","label":"Hypernatremia"}]}},{"entity":"ClinVarVariant:30544","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:35755","phenotype":{"types":[{"id":"HP:0000426","label":"Prominent nasal bridge"}]}},{"entity":"MGI:2445946","phenotype":{"types":[{"id":"MP:0008392","label":"decreased primordial germ cell number"}]}},{"entity":"dbSNP:rs41933638","phenotype":{"types":[{"id":"AQTLTrait:1027","label":"Marbling score"}]}},{"entity":"ClinVarVariant:156148","phenotype":{"types":[{"id":"HP:0001319","label":"Neonatal hypotonia"}]}},{"entity":"ClinVarVariant:5041","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:66431","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"ClinVarVariant:68546","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:2767","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:135705","phenotype":{"types":[{"id":"HP:0100646","label":"Thyroiditis"}]}},{"entity":"FlyBase:FBal0203849","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:100931","phenotype":{"types":[{"id":"HP:0007359","label":"Focal seizures"}]}},{"entity":"MGI:3688879","phenotype":{"types":[{"id":"MP:0010392","label":"prolonged QRS complex duration"}]}},{"entity":"ClinVarVariant:35571","phenotype":{"types":[{"id":"HP:0003073","label":"Hypoalbuminemia"}]}},{"entity":"ClinVarVariant:24365","phenotype":{"types":[{"id":"HP:0000093","label":"Proteinuria"}]}},{"entity":"ClinVarVariant:24419","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:6114","phenotype":{"types":[{"id":"HP:0002510","label":"Spastic tetraplegia"}]}},{"entity":"ClinVarVariant:354","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:11634","phenotype":{"types":[{"id":"HP:0000395","label":"Prominent antihelix"}]}},{"entity":"MGI:3851113","phenotype":{"types":[{"id":"HP:0011472","label":"Abnormality of small intestinal villus morphology"}]}},{"entity":"ClinVarVariant:135899","phenotype":{"types":[{"id":"HP:0000902","label":"Rib fusion"}]}},{"entity":"ClinVarVariant:97681","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"MGI:1857166","phenotype":{"types":[{"id":"HP:0000099","label":"Glomerulonephritis"}]}},{"entity":"MGI:5465004","phenotype":{"types":[{"id":"MP:0011100","label":"preweaning lethality, complete penetrance"}]}},{"entity":"WormBase:WBVar00145415","phenotype":{"types":[{"id":"WBPhenotype:0000695","label":"vulva morphology variant"}]}},{"entity":"ClinVarVariant:189571","phenotype":{"types":[{"id":"HP:0200055","label":"Small hand"}]}},{"entity":"ClinVarVariant:40383","phenotype":{"types":[{"id":"HP:0000962","label":"Hyperkeratosis"}]}},{"entity":"ClinVarVariant:36073","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:49317","phenotype":{"types":[{"id":"HP:0009554","label":"Projection of scalp hair onto lateral cheek"}]}},{"entity":"MGI:1857166","phenotype":{"types":[{"id":"HP:0100494","label":"Abnormality of mast cells"}]}},{"entity":"ClinVarVariant:10725","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"ClinVarVariant:53706","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:68086","phenotype":{"types":[{"id":"HP:0000668","label":"Hypodontia"}]}},{"entity":"MGI:2684151","phenotype":{"types":[{"id":"MP:0000336","label":"decreased mast cell number"}]}},{"entity":"ClinVarVariant:13488","phenotype":{"types":[{"id":"HP:0000776","label":"Congenital diaphragmatic hernia"}]}},{"entity":"ClinVarVariant:42076","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:10987","phenotype":{"types":[{"id":"HP:0002181","label":"Cerebral edema"}]}},{"entity":"ClinVarVariant:7175","phenotype":{"types":[{"id":"HP:0001081","label":"Cholelithiasis"}]}},{"entity":"ClinVarVariant:53953","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:41469","phenotype":{"types":[{"id":"HP:0000239","label":"Large fontanelles"}]}},{"entity":"ClinVarVariant:135726","phenotype":{"types":[{"id":"HP:0007649","label":"Congenital hypertrophy of retinal pigment epithelium"}]}},{"entity":"ClinVarVariant:43595","phenotype":{"types":[{"id":"HP:0030078","label":"Lung adenocarcinoma"}]}},{"entity":"ClinVarVariant:16251","phenotype":{"types":[{"id":"HP:0000869","label":"Secondary amenorrhea"}]}},{"entity":"ClinVarVariant:102","phenotype":{"types":[{"id":"HP:0000987","label":"Atypical scarring of skin"}]}},{"entity":"ClinVarVariant:18054","phenotype":{"types":[{"id":"HP:0002961","label":"Dysgammaglobulinemia"}]}},{"entity":"MGI:2671578","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:136910","phenotype":{"types":[{"id":"HP:0005294","label":"Arterial dissection"}]}},{"entity":"ClinVarVariant:156049","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:216494","phenotype":{"types":[{"id":"HP:0001706","label":"Endocardial fibroelastosis"}]}},{"entity":"MGI:2183405","phenotype":{"types":[{"id":"MP:0009230","label":"abnormal sperm head morphology"}]}},{"entity":"ClinVarVariant:10877","phenotype":{"types":[{"id":"HP:0002872","label":"Apneic episodes precipitated by illness, fatigue, stress"}]}},{"entity":"MGI:1856054","phenotype":{"types":[{"id":"MP:0008892","label":"abnormal sperm flagellum morphology"}]}},{"entity":"ClinVarVariant:208832","phenotype":{"types":[{"id":"HP:0001199","label":"Triphalangeal thumb"}]}},{"entity":"ClinVarVariant:39036","phenotype":{"types":[{"id":"HP:0003026","label":"Short long bone"}]}},{"entity":"ClinVarVariant:68695","phenotype":{"types":[{"id":"HP:0001510","label":"Growth delay"}]}},{"entity":"ClinVarVariant:96338","phenotype":{"types":[{"id":"HP:0004523","label":"Long eyebrows"}]}},{"entity":"MGI:4458398","phenotype":{"types":[{"id":"HP:0005403","label":"T lymphocytopenia"}]}},{"entity":"ClinVarVariant:160087","phenotype":{"types":[{"id":"HP:0000280","label":"Coarse facial features"}]}},{"entity":"ClinVarVariant:262","phenotype":{"types":[{"id":"HP:0007759","label":"Opacification of the corneal stroma"}]}},{"entity":"dbSNP:rs41640954","phenotype":{"types":[{"id":"AQTLTrait:1169","label":"Interval to first estrus after calving"}]}},{"entity":"ClinVarVariant:211747","phenotype":{"types":[{"id":"HP:0000268","label":"Dolichocephaly"}]}},{"entity":"ClinVarVariant:53323","phenotype":{"types":[{"id":"HP:0100651","label":"Type I diabetes mellitus"}]}},{"entity":"ClinVarVariant:216220","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:30844","phenotype":{"types":[{"id":"HP:0010442","label":"Polydactyly"}]}},{"entity":"ClinVarVariant:190358","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"AQTL:162","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"AQTL:29894","phenotype":{"types":[{"id":"AQTLTrait:1081","label":"Age at puberty"}]}},{"entity":"ClinVarVariant:35703","phenotype":{"types":[{"id":"HP:0000934","label":"Chondrocalcinosis"}]}},{"entity":"ClinVarVariant:140986","phenotype":{"types":[{"id":"HP:0002035","label":"Rectal prolapse"}]}},{"entity":"ClinVarVariant:67916","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:189951","phenotype":{"types":[{"id":"HP:0005484","label":"Postnatal microcephaly"}]}},{"entity":"ClinVarVariant:41936","phenotype":{"types":[{"id":"HP:0002435","label":"Meningocele"}]}},{"entity":"AQTL:46123","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:180621","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"ClinVarVariant:216491","phenotype":{"types":[{"id":"HP:0000567","label":"Chorioretinal coloboma"}]}},{"entity":"ClinVarVariant:158375","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"AQTL:5581","phenotype":{"types":[{"id":"AQTLTrait:1181","label":"Muscle pH"}]}},{"entity":"ClinVarVariant:25006","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"ClinVarVariant:60706","phenotype":{"types":[{"id":"HP:0011904","label":"Persistence of hemoglobin F"}]}},{"entity":"ClinVarVariant:17254","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:159655","phenotype":{"types":[{"id":"HP:0000431","label":"Wide nasal bridge"}]}},{"entity":"ClinVarVariant:918","phenotype":{"types":[{"id":"HP:0002748","label":"Rickets"}]}},{"entity":"ClinVarVariant:1519","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:39504","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:11033","phenotype":{"types":[{"id":"HP:0001598","label":"Concave nail"}]}},{"entity":"ClinVarVariant:208834","phenotype":{"types":[{"id":"HP:0008678","label":"Renal hypoplasia/aplasia"}]}},{"entity":"ClinVarVariant:8371","phenotype":{"types":[{"id":"HP:0030325","label":"Cervicomedullary schisis"}]}},{"entity":"ClinVarVariant:21737","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"FlyBase:FBal0204417","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:210031","phenotype":{"types":[{"id":"HP:0000544","label":"External ophthalmoplegia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00016961-WBRNAi00091176","phenotype":{"types":[{"id":"WBPhenotype:0001422","label":"endocytic transport defect"}]}},{"entity":"ClinVarVariant:92727","phenotype":{"types":[{"id":"HP:0002912","label":"Methylmalonic acidemia"}]}},{"entity":"ClinVarVariant:53660","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:42393","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:209009","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"MGI:5548916","phenotype":{"types":[{"id":"MP:0003921","label":"abnormal heart left ventricle morphology"}]}},{"entity":"ClinVarVariant:13366","phenotype":{"types":[{"id":"HP:0001260","label":"Dysarthria"}]}},{"entity":"MGI:5294798","phenotype":{"types":[{"id":"MP:0011087","label":"neonatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:6678","phenotype":{"types":[{"id":"HP:0009025","label":"Increased connective tissue"}]}},{"entity":"MGI:2176538","phenotype":{"types":[{"id":"MP:0011098","label":"embryonic lethality during organogenesis, complete penetrance"}]}},{"entity":"ClinVarVariant:180631","phenotype":{"types":[{"id":"HP:0001433","label":"Hepatosplenomegaly"}]}},{"entity":"ClinVarVariant:4871","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"ClinVarVariant:189559","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-010724-5-ZDB-MRPHLNO-090818-5","phenotype":{"types":[{"id":"ZP:0000043","label":"abnormal(ly) decreased size eye"}]}},{"entity":"ClinVarVariant:186362","phenotype":{"types":[{"id":"HP:0000824","label":"Growth hormone deficiency"}]}},{"entity":"ClinVarVariant:37138","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"ClinVarVariant:10273","phenotype":{"types":[{"id":"HP:0005681","label":"Juvenile rheumatoid arthritis"}]}},{"entity":"ClinVarVariant:1035","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:65024","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:56203","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:8762","phenotype":{"types":[{"id":"HP:0008066","label":"Abnormal blistering of the skin"}]}},{"entity":"ZFIN:ZDB-ALT-070315-12","phenotype":{"types":[{"id":"ZP:0008827","label":"abnormal(ly) process quality branchiomeric skeletal muscle development"}]}},{"entity":"ClinVarVariant:6212","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:162385","phenotype":{"types":[{"id":"HP:0000998","label":"Hypertrichosis"}]}},{"entity":"dbSNP:rs41607431","phenotype":{"types":[{"id":"AQTLTrait:1115","label":"Chest width"}]}},{"entity":"ClinVarVariant:35706","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:54083","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:183262","phenotype":{"types":[{"id":"HP:0100689","label":"Decreased corneal thickness"}]}},{"entity":"ClinVarVariant:156109","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"MGI:3579250","phenotype":{"types":[{"id":"MP:0000229","label":"abnormal megakaryocyte differentiation"}]}},{"entity":"ClinVarVariant:83199","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"AQTL:40463","phenotype":{"types":[{"id":"AQTLTrait:1136","label":"Bone quality"}]}},{"entity":"WormBase:WBVar00252381","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:53600","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:93198","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"NCBIGene:474168","phenotype":{"types":[{"id":"HP:0000099","label":"Glomerulonephritis"}]}},{"entity":"ClinVarVariant:194859","phenotype":{"types":[{"id":"HP:0000256","label":"Macrocephaly"}]}},{"entity":"ClinVarVariant:30723","phenotype":{"types":[{"id":"HP:0007360","label":"Aplasia/Hypoplasia of the cerebellum"}]}},{"entity":"ClinVarVariant:25245","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:158580","phenotype":{"types":[{"id":"HP:0002002","label":"Deep philtrum"}]}},{"entity":"MGI:5444021","phenotype":{"types":[{"id":"MP:0001360","label":"abnormal social investigation"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-041212-76-ZDB-MRPHLNO-090513-3","phenotype":{"types":[{"id":"GO:0007368PHENOTYPE","label":"determination of left/right symmetry phenotype"}]}},{"entity":"ClinVarVariant:203516","phenotype":{"types":[{"id":"HP:0002841","label":"Recurrent fungal infections"}]}},{"entity":"ClinVarVariant:160035","phenotype":{"types":[{"id":"HP:0000430","label":"Underdeveloped nasal alae"}]}},{"entity":"ClinVarVariant:137952","phenotype":{"types":[{"id":"HP:0001841","label":"Preaxial foot polydactyly"}]}},{"entity":"ClinVarVariant:41170","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:49531","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:10128","phenotype":{"types":[{"id":"HP:0005542","label":"Prolonged whole-blood clotting time"}]}},{"entity":"ClinVarVariant:179061","phenotype":{"types":[{"id":"HP:0000691","label":"Microdontia"}]}},{"entity":"ClinVarVariant:136113","phenotype":{"types":[{"id":"HP:0000980","label":"Pallor"}]}},{"entity":"ClinVarVariant:198428","phenotype":{"types":[{"id":"HP:0004396","label":"Poor appetite"}]}},{"entity":"ClinVarVariant:92639","phenotype":{"types":[{"id":"HP:0100729","label":"Large face"}]}},{"entity":"ClinVarVariant:53923","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:16873","phenotype":{"types":[{"id":"HP:0002716","label":"Lymphadenopathy"}]}},{"entity":"ClinVarVariant:35866","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"ClinVarVariant:54000","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:53479","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:36062","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"MGI:1934269","phenotype":{"types":[{"id":"HP:0005506","label":"Chronic myelogenous leukemia"}]}},{"entity":"ClinVarVariant:31696","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:1720","phenotype":{"types":[{"id":"HP:0001511","label":"Intrauterine growth retardation"}]}},{"entity":"ClinVarVariant:3193","phenotype":{"types":[{"id":"HP:0008829","label":"Delayed femoral head ossification"}]}},{"entity":"MGI:5538688","phenotype":{"types":[{"id":"HP:0008734","label":"Decreased testicular size"}]}},{"entity":"ClinVarVariant:56181","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:66051","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:16327","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"ClinVarVariant:75243","phenotype":{"types":[{"id":"HP:0100034","label":"Motor tics"}]}},{"entity":"MGI:2679499","phenotype":{"types":[{"id":"GO:0009887PHENOTYPE","label":"organ morphogenesis phenotype"}]}},{"entity":"ClinVarVariant:31210","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:13045","phenotype":{"types":[{"id":"HP:0001123","label":"Visual field defect"}]}},{"entity":"ClinVarVariant:179632","phenotype":{"types":[{"id":"HP:0004937","label":"Pulmonary artery aneurysm"}]}},{"entity":"ClinVarVariant:1866","phenotype":{"types":[{"id":"HP:0002315","label":"Headache"}]}},{"entity":"ClinVarVariant:29652","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ZFIN:ZDB-ALT-980203-386","phenotype":{"types":[{"id":"ZP:0000528","label":"abnormal(ly) decreased size cardiac ventricle"}]}},{"entity":"ClinVarVariant:204218","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:211647","phenotype":{"types":[{"id":"HP:0000776","label":"Congenital diaphragmatic hernia"}]}},{"entity":"ClinVarVariant:67368","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001500-WBRNAi00038528","phenotype":{"types":[{"id":"WBPhenotype:0002046","label":"iron homeostasis variant"}]}},{"entity":"ClinVarVariant:49541","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"MGI:3697906","phenotype":{"types":[{"id":"HP:0000234","label":"Abnormality of the head"}]}},{"entity":"ClinVarVariant:198399","phenotype":{"types":[{"id":"HP:0001279","label":"Syncope"}]}},{"entity":"FlyBase:FBal0294194","phenotype":{"types":[{"id":"FBbt:00004133PHENOTYPE","label":"interommatidial bristle phenotype"}]}},{"entity":"ClinVarVariant:95419","phenotype":{"types":[{"id":"HP:0003487","label":"Babinski sign"}]}},{"entity":"ClinVarVariant:1331","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"ClinVarVariant:162400","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"ClinVarVariant:120300","phenotype":{"types":[{"id":"HP:0002071","label":"Abnormality of extrapyramidal motor function"}]}},{"entity":"ClinVarVariant:7315","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"ClinVarVariant:65617","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"MGI:4356015","phenotype":{"types":[{"id":"MP:0005222","label":"abnormal somite size"}]}},{"entity":"ClinVarVariant:24990","phenotype":{"types":[{"id":"HP:0200042","label":"Skin ulcer"}]}},{"entity":"ClinVarVariant:53350","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:1010","phenotype":{"types":[{"id":"HP:0000512","label":"Abnormal electroretinogram"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001186-WBRNAi00086860","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:92545","phenotype":{"types":[{"id":"HP:0002326","label":"Transient ischemic attack"}]}},{"entity":"ClinVarVariant:38726","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:191776","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"FlyBase:FBal0031399","phenotype":{"types":[{"id":"FBbt:00004233PHENOTYPE","label":"Drosophila tertiary pigment cell phenotype"}]}},{"entity":"ClinVarVariant:188299","phenotype":{"types":[{"id":"HP:0010610","label":"Palmar pits"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00044585-WBRNAi00024788","phenotype":{"types":[{"id":"WBPhenotype:0000643","label":"locomotion variant"}]}},{"entity":"ClinVarVariant:42130","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:49521","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"MGI:2137552","phenotype":{"types":[{"id":"MP:0003935","label":"abnormal craniofacial development"}]}},{"entity":"ClinVarVariant:38629","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"ClinVarVariant:143768","phenotype":{"types":[{"id":"HP:0000478","label":"Abnormality of the eye"}]}},{"entity":"ClinVarVariant:24826","phenotype":{"types":[{"id":"HP:0001636","label":"Tetralogy of Fallot"}]}},{"entity":"ClinVarVariant:850","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019835-WBRNAi00082433","phenotype":{"types":[{"id":"WBPhenotype:0001037","label":"sterile progeny"}]}},{"entity":"ClinVarVariant:7185","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:17284","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:24656","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"FlyBase:FBal0276873","phenotype":{"types":[{"id":"FBbt:00004508PHENOTYPE","label":"eye phenotype"}]}},{"entity":"AQTL:24787","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:11850","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"MGI:5297423","phenotype":{"types":[{"id":"HP:0001719","label":"Double outlet right ventricle"}]}},{"entity":"ClinVarVariant:12041","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:53725","phenotype":{"types":[{"id":"HP:0004936","label":"Venous thrombosis"}]}},{"entity":"ClinVarVariant:42355","phenotype":{"types":[{"id":"HP:0004933","label":"Ascending aortic dissection"}]}},{"entity":"ClinVarVariant:24265","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"ClinVarVariant:2264","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"MGI:1857632","phenotype":{"types":[{"id":"MP:0004342","label":"scapular bone foramen"}]}},{"entity":"MGI:3526866","phenotype":{"types":[{"id":"MP:0000157","label":"abnormal sternum morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00009498-WBRNAi00085795","phenotype":{"types":[{"id":"WBPhenotype:0001952","label":"germline nuclear positioning variant"}]}},{"entity":"ClinVarVariant:4135","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"ClinVarVariant:54063","phenotype":{"types":[{"id":"HP:0000966","label":"Hypohidrosis"}]}},{"entity":"ClinVarVariant:159076","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:192290","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"ClinVarVariant:167144","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:143120","phenotype":{"types":[{"id":"HP:0000622","label":"Blurred vision"}]}},{"entity":"FlyBase:FBal0294983","phenotype":{"types":[{"id":"FBcv:0000385","label":"short lived"}]}},{"entity":"ClinVarVariant:42317","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"ClinVarVariant:53732","phenotype":{"types":[{"id":"HP:0011947","label":"Respiratory tract infection"}]}},{"entity":"ClinVarVariant:11668","phenotype":{"types":[{"id":"HP:0000498","label":"Blepharitis"}]}},{"entity":"ClinVarVariant:30851","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:13153","phenotype":{"types":[{"id":"HP:0001874","label":"Abnormality of neutrophils"}]}},{"entity":"ClinVarVariant:101354","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"MGI:5522949","phenotype":{"types":[{"id":"MP:0002662","label":"abnormal cauda epididymis morphology"}]}},{"entity":"ClinVarVariant:30182","phenotype":{"types":[{"id":"HP:0003312","label":"Abnormal form of the vertebral bodies"}]}},{"entity":"ClinVarVariant:11114","phenotype":{"types":[{"id":"HP:0001891","label":"Iron deficiency anemia"}]}},{"entity":"ClinVarVariant:10735","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"FlyBase:FBal0095354","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:41334","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:5424","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"ClinVarVariant:12981","phenotype":{"types":[{"id":"HP:0003324","label":"Generalized muscle weakness"}]}},{"entity":"ClinVarVariant:216845","phenotype":{"types":[{"id":"HP:0001663","label":"Ventricular fibrillation"}]}},{"entity":"ClinVarVariant:142378","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:163768","phenotype":{"types":[{"id":"HP:0000766","label":"Abnormality of the sternum"}]}},{"entity":"ClinVarVariant:40069","phenotype":{"types":[{"id":"HP:0000110","label":"Renal dysplasia"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-060503-240-ZDB-MRPHLNO-101202-1","phenotype":{"types":[{"id":"ZP:0003746","label":"abnormal(ly) delayed angiogenesis"}]}},{"entity":"ClinVarVariant:195329","phenotype":{"types":[{"id":"HP:0000368","label":"Low-set, posteriorly rotated ears"}]}},{"entity":"ClinVarVariant:40249","phenotype":{"types":[{"id":"HP:0100704","label":"Cortical visual impairment"}]}},{"entity":"ClinVarVariant:95454","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:41252","phenotype":{"types":[{"id":"HP:0010298","label":"Smooth tongue"}]}},{"entity":"dbSNP:rs41571256","phenotype":{"types":[{"id":"AQTLTrait:1070","label":"Inseminations per conception"}]}},{"entity":"ClinVarVariant:210016","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:42382","phenotype":{"types":[{"id":"HP:0001380","label":"Ligamentous laxity"}]}},{"entity":"MGI:3530566","phenotype":{"types":[{"id":"HP:0000135","label":"Hypogonadism"}]}},{"entity":"ClinVarVariant:40452","phenotype":{"types":[{"id":"HP:0003510","label":"Severe short stature"}]}},{"entity":"ClinVarVariant:17294","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:36530","phenotype":{"types":[{"id":"HP:0003072","label":"Hypercalcemia"}]}},{"entity":"ClinVarVariant:216568","phenotype":{"types":[{"id":"HP:0002665","label":"Lymphoma"}]}},{"entity":"ClinVarVariant:38909","phenotype":{"types":[{"id":"HP:0003521","label":"Disproportionate short-trunk short stature"}]}},{"entity":"_:genid1939651","phenotype":{"types":[{"id":"ZP:0000335","label":"abnormal(ly) disrupted blood circulation"}]}},{"entity":"ClinVarVariant:42333","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"ClinVarVariant:101286","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:100762","phenotype":{"types":[{"id":"HP:0000174","label":"Abnormality of the palate"}]}},{"entity":"ClinVarVariant:10997","phenotype":{"types":[{"id":"HP:0002181","label":"Cerebral edema"}]}},{"entity":"ClinVarVariant:91680","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:211317","phenotype":{"types":[{"id":"HP:0003312","label":"Abnormal form of the vertebral bodies"}]}},{"entity":"ClinVarVariant:25103","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:159952","phenotype":{"types":[{"id":"HP:0100627","label":"Displacement of the external urethral meatus"}]}},{"entity":"_:genid1976450","phenotype":{"types":[{"id":"ZP:0000038","label":"abnormal(ly) edematous pericardium"}]}},{"entity":"ClinVarVariant:10745","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"dbSNP:rs7756992","phenotype":{"types":[{"id":"HP:0002155","label":"Hypertriglyceridemia"}]}},{"entity":"ClinVarVariant:24583","phenotype":{"types":[{"id":"HP:0010784","label":"Uterine neoplasm"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007008-WBRNAi00064202","phenotype":{"types":[{"id":"WBPhenotype:0000730","label":"apoptosis variant"}]}},{"entity":"ClinVarVariant:9589","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:12788","phenotype":{"types":[{"id":"HP:0011976","label":"Elevated urinary catecholamines"}]}},{"entity":"ClinVarVariant:216729","phenotype":{"types":[{"id":"HP:0100634","label":"Neuroendocrine neoplasm"}]}},{"entity":"MGI:2446069","phenotype":{"types":[{"id":"MP:0008395","label":"abnormal osteoblast differentiation"}]}},{"entity":"ClinVarVariant:14356","phenotype":{"types":[{"id":"HP:0007657","label":"Diffuse nuclear cataract"}]}},{"entity":"ClinVarVariant:7834","phenotype":{"types":[{"id":"HP:0004481","label":"Progressive macrocephaly"}]}},{"entity":"ClinVarVariant:210404","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"WormBase:WBVar00145377","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:16275","phenotype":{"types":[{"id":"HP:0002667","label":"Nephroblastoma (Wilms tumor)"}]}},{"entity":"ClinVarVariant:158319","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:42114","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:210436","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"ClinVarVariant:39026","phenotype":{"types":[{"id":"HP:0003026","label":"Short long bone"}]}},{"entity":"MGI:1856392","phenotype":{"types":[{"id":"HP:0007544","label":"Piebaldism"}]}},{"entity":"dbSNP:rs29010222","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:53535","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000817-WBRNAi00086749","phenotype":{"types":[{"id":"WBPhenotype:0001036","label":"sterile F1"}]}},{"entity":"ClinVarVariant:143264","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"ClinVarVariant:53943","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:53493","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:159024","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"ClinVarVariant:215698","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:55951","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:60536","phenotype":{"types":[{"id":"HP:0002172","label":"Postural instability"}]}},{"entity":"ClinVarVariant:48816","phenotype":{"types":[{"id":"HP:0009720","label":"Adenoma sebaceum"}]}},{"entity":"MGI:3774018","phenotype":{"types":[{"id":"MP:0011087","label":"neonatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:49510","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:56213","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:156160","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"MGI:5646298","phenotype":{"types":[{"id":"HP:0002180","label":"Neurodegeneration"}]}},{"entity":"ClinVarVariant:21525","phenotype":{"types":[{"id":"HP:0001256","label":"Intellectual disability, mild"}]}},{"entity":"ClinVarVariant:4311","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"AQTL:5929","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"FlyBase:FBal0269430","phenotype":{"types":[{"id":"FBbt:00002743PHENOTYPE","label":"Drosophila T1 beard phenotype"}]}},{"entity":"ClinVarVariant:31675","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"ClinVarVariant:49257","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"NCBIGene:100188011","phenotype":{"types":[{"id":"HP:0002789","label":"Tachypnea"}]}},{"entity":"ClinVarVariant:136120","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:2722","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"FlyBase:FBal0124416","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:156720","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"WormBase:WBVar00248887","phenotype":{"types":[{"id":"WBPhenotype:0000698","label":"vulvaless"}]}},{"entity":"ClinVarVariant:40706","phenotype":{"types":[{"id":"HP:0000027","label":"Azoospermia"}]}},{"entity":"ClinVarVariant:13836","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:56096","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"ClinVarVariant:41513","phenotype":{"types":[{"id":"HP:0002895","label":"Papillary thyroid carcinoma"}]}},{"entity":"ClinVarVariant:17374","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:40493","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:49571","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"NCBIGene:46","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"ClinVarVariant:9303","phenotype":{"types":[{"id":"HP:0000340","label":"Sloping forehead"}]}},{"entity":"ClinVarVariant:3853","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:133101","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:53206","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"dbSNP:rs41937398","phenotype":{"types":[{"id":"AQTLTrait:1101","label":"Foot angle"}]}},{"entity":"ClinVarVariant:10275","phenotype":{"types":[{"id":"HP:0001369","label":"Arthritis"}]}},{"entity":"ClinVarVariant:54004","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:15326","phenotype":{"types":[{"id":"HP:0011031","label":"Abnormality of iron homeostasis"}]}},{"entity":"ClinVarVariant:92555","phenotype":{"types":[{"id":"HP:0002326","label":"Transient ischemic attack"}]}},{"entity":"ClinVarVariant:49551","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:94537","phenotype":{"types":[{"id":"HP:0006466","label":"Ankle contracture"}]}},{"entity":"ClinVarVariant:143160","phenotype":{"types":[{"id":"HP:0003474","label":"Sensory impairment"}]}},{"entity":"ClinVarVariant:135685","phenotype":{"types":[{"id":"HP:0008069","label":"Neoplasm of the skin"}]}},{"entity":"ClinVarVariant:2251","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:1525","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:50993","phenotype":{"types":[{"id":"HP:0009882","label":"Short distal phalanx of finger"}]}},{"entity":"MGI:2678815","phenotype":{"types":[{"id":"MP:0001212","label":"skin lesions"}]}},{"entity":"ClinVarVariant:7155","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001924-WBRNAi00068386","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:92747","phenotype":{"types":[{"id":"HP:0002912","label":"Methylmalonic acidemia"}]}},{"entity":"ClinVarVariant:30040","phenotype":{"types":[{"id":"HP:0000311","label":"Round face"}]}},{"entity":"ClinVarVariant:180277","phenotype":{"types":[{"id":"HP:0001084","label":"Corneal arcus"}]}},{"entity":"ClinVarVariant:36438","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:38950","phenotype":{"types":[{"id":"HP:0001876","label":"Pancytopenia"}]}},{"entity":"ClinVarVariant:93752","phenotype":{"types":[{"id":"HP:0000668","label":"Hypodontia"}]}},{"entity":"ClinVarVariant:14184","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"MGI:4840274","phenotype":{"types":[{"id":"MP:0008185","label":"decreased naive B cell number"}]}},{"entity":"MGI:1857225","phenotype":{"types":[{"id":"MP:0008189","label":"increased transitional stage B cell number"}]}},{"entity":"ClinVarVariant:215688","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:30293","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:4354","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"ClinVarVariant:50061","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:94691","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:189113","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:53297","phenotype":{"types":[{"id":"HP:0001648","label":"Cor pulmonale"}]}},{"entity":"MGI:5463664","phenotype":{"types":[{"id":"HP:0002910","label":"Elevated hepatic transaminases"}]}},{"entity":"ClinVarVariant:188272","phenotype":{"types":[{"id":"HP:0000892","label":"Bifid ribs"}]}},{"entity":"ClinVarVariant:65895","phenotype":{"types":[{"id":"HP:0001392","label":"Abnormality of the liver"}]}},{"entity":"ClinVarVariant:53356","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004010-WBRNAi00063019","phenotype":{"types":[{"id":"WBPhenotype:0000709","label":"pharyngeal morphology variant"}]}},{"entity":"ClinVarVariant:167303","phenotype":{"types":[{"id":"HP:0008368","label":"Tarsal synostosis"}]}},{"entity":"ClinVarVariant:132708","phenotype":{"types":[{"id":"HP:0009919","label":"Retinoblastoma"}]}},{"entity":"ClinVarVariant:36314","phenotype":{"types":[{"id":"HP:0002835","label":"Aspiration"}]}},{"entity":"MGI:1858064","phenotype":{"types":[{"id":"GO:0043473PHENOTYPE","label":"pigmentation phenotype"}]}},{"entity":"ClinVarVariant:49462","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:53481","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:9008","phenotype":{"types":[{"id":"HP:0004383","label":"Hypoplastic left heart"}]}},{"entity":"ClinVarVariant:210444","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ZFIN:ZDB-ALT-040726-6","phenotype":{"types":[{"id":"ZP:0002272","label":"abnormal(ly) necrotic brain"}]}},{"entity":"ClinVarVariant:13693","phenotype":{"types":[{"id":"HP:0001082","label":"Cholecystitis"}]}},{"entity":"ClinVarVariant:133328","phenotype":{"types":[{"id":"HP:0012448","label":"Delayed myelination"}]}},{"entity":"FlyBase:FBal0058766","phenotype":{"types":[{"id":"FBcv:0000386","label":"long lived"}]}},{"entity":"ClinVarVariant:65285","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"MGI:4412094","phenotype":{"types":[{"id":"MP:0000260","label":"abnormal angiogenesis"}]}},{"entity":"ClinVarVariant:66461","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"ClinVarVariant:65104","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:2036","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:4330","phenotype":{"types":[{"id":"HP:0003540","label":"Impaired platelet aggregation"}]}},{"entity":"ClinVarVariant:36092","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"AQTL:15021","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:53931","phenotype":{"types":[{"id":"HP:0003453","label":"Antineutrophil antibody positivity"}]}},{"entity":"ClinVarVariant:210006","phenotype":{"types":[{"id":"HP:0002140","label":"Ischemic stroke"}]}},{"entity":"dbSNP:rs110432080","phenotype":{"types":[{"id":"AQTLTrait:1253","label":"Milk stearic acid percentage"}]}},{"entity":"ClinVarVariant:53690","phenotype":{"types":[{"id":"HP:0011947","label":"Respiratory tract infection"}]}},{"entity":"ClinVarVariant:2568","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:136042","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:9723","phenotype":{"types":[{"id":"HP:0002083","label":"Migraine without aura"}]}},{"entity":"FlyBase:FBal0207483","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:133175","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:68701","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:10144","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:101122","phenotype":{"types":[{"id":"HP:0000490","label":"Deeply set eye"}]}},{"entity":"MGI:3054057","phenotype":{"types":[{"id":"HP:0003110","label":"Abnormality of urine homeostasis"}]}},{"entity":"NCBIGene:100188278","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:38317","phenotype":{"types":[{"id":"HP:0000089","label":"Renal hypoplasia"}]}},{"entity":"ClinVarVariant:2139","phenotype":{"types":[{"id":"HP:0002036","label":"Hiatus hernia"}]}},{"entity":"ClinVarVariant:143572","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:215586","phenotype":{"types":[{"id":"HP:0005550","label":"Chronic lymphatic leukemia"}]}},{"entity":"ClinVarVariant:100930","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:53953","phenotype":{"types":[{"id":"HP:0011950","label":"Bronchiolitis"}]}},{"entity":"ClinVarVariant:82650","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"WormBase:WBVar00242504","phenotype":{"types":[{"id":"WBPhenotype:0000012","label":"dauer constitutive"}]}},{"entity":"ClinVarVariant:65311","phenotype":{"types":[{"id":"HP:0003764","label":"Nevus"}]}},{"entity":"ClinVarVariant:158661","phenotype":{"types":[{"id":"HP:0009937","label":"Facial hirsutism"}]}},{"entity":"ClinVarVariant:30293","phenotype":{"types":[{"id":"HP:0000632","label":"Lacrimation abnormality"}]}},{"entity":"dbSNP:rs109839918","phenotype":{"types":[{"id":"AQTLTrait:1096","label":"Teat length"}]}},{"entity":"ClinVarVariant:39868","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:10014","phenotype":{"types":[{"id":"HP:0030344","label":"Decreased circulating luteinizing hormone level"}]}},{"entity":"ClinVarVariant:145","phenotype":{"types":[{"id":"HP:0001308","label":"Tongue fasciculations"}]}},{"entity":"ClinVarVariant:10692","phenotype":{"types":[{"id":"HP:0100639","label":"Erectile abnormalities"}]}},{"entity":"ClinVarVariant:36096","phenotype":{"types":[{"id":"HP:0001002","label":"Decreased subcutaneous fat"}]}},{"entity":"ClinVarVariant:8643","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"FlyBase:FBal0207769","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017546-WBRNAi00099316","phenotype":{"types":[{"id":"WBPhenotype:0000961","label":"pattern of transgene expression variant"}]}},{"entity":"ClinVarVariant:30964","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001972-WBRNAi00068412","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:143515","phenotype":{"types":[{"id":"HP:0000729","label":"Autistic behavior"}]}},{"entity":"ClinVarVariant:54014","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:45003","phenotype":{"types":[{"id":"HP:0011034","label":"Amyloidosis"}]}},{"entity":"MGI:5286584","phenotype":{"types":[{"id":"HP:0002446","label":"Astrocytosis"}]}},{"entity":"ClinVarVariant:43601","phenotype":{"types":[{"id":"HP:0009726","label":"Renal neoplasm"}]}},{"entity":"OMIM:220210","phenotype":{"types":[{"id":"HP:0010935","label":"Abnormality of the upper urinary tract"}]}},{"entity":"ClinVarVariant:210485","phenotype":{"types":[{"id":"HP:0007327","label":"Mixed demyelinating and axonal polyneuropathy"}]}},{"entity":"ClinVarVariant:36754","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"ClinVarVariant:67997","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"dbSNP:rs1819084","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:12604","phenotype":{"types":[{"id":"HP:0001067","label":"Neurofibromas"}]}},{"entity":"ClinVarVariant:156003","phenotype":{"types":[{"id":"HP:0100533","label":"Inflammatory abnormality of the eye"}]}},{"entity":"ClinVarVariant:25300","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:92575","phenotype":{"types":[{"id":"HP:0002326","label":"Transient ischemic attack"}]}},{"entity":"ClinVarVariant:66481","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"ClinVarVariant:50259","phenotype":{"types":[{"id":"HP:0005897","label":"Severe generalized osteoporosis"}]}},{"entity":"ClinVarVariant:53876","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:208009","phenotype":{"types":[{"id":"HP:0001482","label":"Subcutaneous nodule"}]}},{"entity":"FlyBase:FBal0239575","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004815-WBRNAi00086787","phenotype":{"types":[{"id":"WBPhenotype:0000793","label":"posterior body morphology variant"}]}},{"entity":"ClinVarVariant:101152","phenotype":{"types":[{"id":"HP:0010318","label":"Aplasia/Hypoplasia of the abdominal wall musculature"}]}},{"entity":"ClinVarVariant:97040","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"ClinVarVariant:6794","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"dbSNP:rs41859871","phenotype":{"types":[{"id":"AQTLTrait:1292","label":"Early embryonic survival"}]}},{"entity":"ClinVarVariant:10755","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"ClinVarVariant:10609","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:159081","phenotype":{"types":[{"id":"HP:0000752","label":"Hyperactivity"}]}},{"entity":"ClinVarVariant:9973","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:102433","phenotype":{"types":[{"id":"HP:0003128","label":"Lactic acidosis"}]}},{"entity":"MGI:2176174","phenotype":{"types":[{"id":"MP:0011028","label":"impaired branching involved in bronchus morphogenesis"}]}},{"entity":"ClinVarVariant:64987","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"dbSNP:rs4793501","phenotype":{"types":[{"id":"HP:0000539","label":"Abnormality of refraction"}]}},{"entity":"ClinVarVariant:18337","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:36520","phenotype":{"types":[{"id":"HP:0003072","label":"Hypercalcemia"}]}},{"entity":"ClinVarVariant:91670","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"AQTL:10280","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:204086","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"_:genid1972511","phenotype":{"types":[{"id":"ZP:0002787","label":"abnormal(ly) decreased size intestinal epithelium"}]}},{"entity":"FlyBase:FBal0047091","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"MGI:4941848","phenotype":{"types":[{"id":"MP:0003956","label":"abnormal body size"}]}},{"entity":"ClinVarVariant:36381","phenotype":{"types":[{"id":"HP:0001597","label":"Abnormality of the nail"}]}},{"entity":"ClinVarVariant:53524","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"ClinVarVariant:177959","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:53340","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:1379","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:9877","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:7188","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:2149","phenotype":{"types":[{"id":"HP:0002036","label":"Hiatus hernia"}]}},{"entity":"dbSNP:rs11986414","phenotype":{"types":[{"id":"HP:0001433","label":"Hepatosplenomegaly"}]}},{"entity":"ClinVarVariant:13335","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:9946","phenotype":{"types":[{"id":"HP:0001923","label":"Reticulocytosis"}]}},{"entity":"ClinVarVariant:10239","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:3042795","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:90871","phenotype":{"types":[{"id":"HP:0100574","label":"Biliary tract neoplasm"}]}},{"entity":"WormBase:WBVar00146684","phenotype":{"types":[{"id":"WBPhenotype:0001846","label":"phagosome maturation defective"}]}},{"entity":"ClinVarVariant:216715","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006994-WBRNAi00088835","phenotype":{"types":[{"id":"WBPhenotype:0001588","label":"microtubule organization biogenesis variant"}]}},{"entity":"ClinVarVariant:91320","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:65118","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:208580","phenotype":{"types":[{"id":"HP:0002414","label":"Spina bifida"}]}},{"entity":"ClinVarVariant:9733","phenotype":{"types":[{"id":"HP:0002083","label":"Migraine without aura"}]}},{"entity":"ClinVarVariant:141815","phenotype":{"types":[{"id":"HP:0002017","label":"Nausea and vomiting"}]}},{"entity":"ClinVarVariant:24826","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ClinVarVariant:41655","phenotype":{"types":[{"id":"HP:0100730","label":"Bronchogenic cyst"}]}},{"entity":"ClinVarVariant:24361","phenotype":{"types":[{"id":"HP:0200020","label":"Corneal erosion"}]}},{"entity":"FlyBase:FBal0314224","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:2261","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:10335","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:30910","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"ClinVarVariant:53636","phenotype":{"types":[{"id":"HP:0006510","label":"Chronic obstructive pulmonary disease"}]}},{"entity":"ClinVarVariant:44804","phenotype":{"types":[{"id":"HP:0000368","label":"Low-set, posteriorly rotated ears"}]}},{"entity":"ClinVarVariant:36071","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:2199","phenotype":{"types":[{"id":"HP:0000408","label":"Progressive sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:11934","phenotype":{"types":[{"id":"HP:0002315","label":"Headache"}]}},{"entity":"ClinVarVariant:53728","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:21555","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019126-WBRNAi00091874","phenotype":{"types":[{"id":"WBPhenotype:0001372","label":"protein DNA interaction variant"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001177-WBRNAi00088701","phenotype":{"types":[{"id":"WBPhenotype:0002059","label":"pore forming toxin hypersensitive"}]}},{"entity":"ClinVarVariant:53284","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000866-WBRNAi00007858","phenotype":{"types":[{"id":"WBPhenotype:0001083","label":"multiple cytoplasmic cavities early emb"}]}},{"entity":"FlyBase:FBal0278276","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:95624","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:819","phenotype":{"types":[{"id":"HP:0200040","label":"Epidermoid cyst"}]}},{"entity":"ClinVarVariant:38806","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"AQTL:49870","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:5142","phenotype":{"types":[{"id":"HP:0000144","label":"Decreased fertility"}]}},{"entity":"ClinVarVariant:53188","phenotype":{"types":[{"id":"HP:0004395","label":"Malnutrition"}]}},{"entity":"ClinVarVariant:194962","phenotype":{"types":[{"id":"HP:0001608","label":"Abnormality of the voice"}]}},{"entity":"ClinVarVariant:159224","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:101105","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"AQTL:11222","phenotype":{"types":[{"id":"AQTLTrait:1027","label":"Marbling score"}]}},{"entity":"ClinVarVariant:64789","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"WormBase:WBVar00250996","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:49591","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"FlyBase:FBal0209601","phenotype":{"types":[{"id":"FBcv:0000385","label":"short lived"}]}},{"entity":"MGI:2678247","phenotype":{"types":[{"id":"MP:0004768","label":"abnormal axonal transport"}]}},{"entity":"ClinVarVariant:30231","phenotype":{"types":[{"id":"HP:0000527","label":"Long eyelashes"}]}},{"entity":"ClinVarVariant:136202","phenotype":{"types":[{"id":"HP:0000750","label":"Delayed speech and language development"}]}},{"entity":"MGI:5620941","phenotype":{"types":[{"id":"MP:0003098","label":"decreased tendon stiffness"}]}},{"entity":"ClinVarVariant:9818","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:38486","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"ClinVarVariant:210414","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:10727","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"ClinVarVariant:49581","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:16209","phenotype":{"types":[{"id":"HP:0010819","label":"Atonic seizures"}]}},{"entity":"ClinVarVariant:7199","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:36791","phenotype":{"types":[{"id":"HP:0006335","label":"Persistence of primary teeth"}]}},{"entity":"MGI:2429699","phenotype":{"types":[{"id":"HP:0012373","label":"Abnormal eye physiology"}]}},{"entity":"AQTL:16489","phenotype":{"types":[{"id":"AQTLTrait:1173","label":"Rear leg set"}]}},{"entity":"ClinVarVariant:41523","phenotype":{"types":[{"id":"HP:0002895","label":"Papillary thyroid carcinoma"}]}},{"entity":"ClinVarVariant:159218","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"ClinVarVariant:158734","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"ClinVarVariant:156221","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"ClinVarVariant:53913","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:141514","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"MGI:4364926","phenotype":{"types":[{"id":"HP:0011877","label":"Increased mean platelet volume"}]}},{"entity":"MGI:1856226","phenotype":{"types":[{"id":"MP:0001265","label":"decreased body size"}]}},{"entity":"ClinVarVariant:159380","phenotype":{"types":[{"id":"HP:0009890","label":"High anterior hairline"}]}},{"entity":"ClinVarVariant:160081","phenotype":{"types":[{"id":"HP:0001298","label":"Encephalopathy"}]}},{"entity":"FlyBase:FBal0210535","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:127501","phenotype":{"types":[{"id":"HP:0000268","label":"Dolichocephaly"}]}},{"entity":"FlyBase:FBal0242677","phenotype":{"types":[{"id":"FBbt:00002027PHENOTYPE","label":"Drosophila dorsal multidendritic neuron ddaC phenotype"}]}},{"entity":"ClinVarVariant:5539","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"ClinVarVariant:88731","phenotype":{"types":[{"id":"HP:0002307","label":"Drooling"}]}},{"entity":"FlyBase:FBal0230781","phenotype":{"types":[{"id":"FBcv:0002027","label":"lethal - all die before end of pupal stage"}]}},{"entity":"ClinVarVariant:197858","phenotype":{"types":[{"id":"HP:0003300","label":"Ovoid vertebral bodies"}]}},{"entity":"FlyBase:FBal0137561","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:120310","phenotype":{"types":[{"id":"HP:0002071","label":"Abnormality of extrapyramidal motor function"}]}},{"entity":"ClinVarVariant:210018","phenotype":{"types":[{"id":"HP:0009113","label":"Diaphragmatic weakness"}]}},{"entity":"ClinVarVariant:25297","phenotype":{"types":[{"id":"HP:0008209","label":"Premature ovarian failure"}]}},{"entity":"MGI:5527244","phenotype":{"types":[{"id":"HP:0100522","label":"Thymoma"}]}},{"entity":"ClinVarVariant:53175","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"ClinVarVariant:2365","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:4142","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:6915","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:53881","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:94530","phenotype":{"types":[{"id":"HP:0100578","label":"Lipoatrophy"}]}},{"entity":"ClinVarVariant:215763","phenotype":{"types":[{"id":"HP:0100242","label":"Sarcoma"}]}},{"entity":"ClinVarVariant:222","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:10741","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:1113","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:67871","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"MGI:1931047","phenotype":{"types":[{"id":"MP:0010572","label":"persistent right dorsal aorta"}]}},{"entity":"ClinVarVariant:48708","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:30249","phenotype":{"types":[{"id":"HP:0000046","label":"Scrotal hypoplasia"}]}},{"entity":"ClinVarVariant:128250","phenotype":{"types":[{"id":"HP:0002490","label":"Increased CSF lactate"}]}},{"entity":"ClinVarVariant:41075","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"WormBase:WBVar00142906","phenotype":{"types":[{"id":"WBPhenotype:0001516","label":"helical cuticle"}]}},{"entity":"MGI:3837468","phenotype":{"types":[{"id":"HP:0004324","label":"Increased body weight"}]}},{"entity":"WormBase:WBVar00143933","phenotype":{"types":[{"id":"WBPhenotype:0000905","label":"neuron morphology variant"}]}},{"entity":"ClinVarVariant:10078","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"MGI:4442818","phenotype":{"types":[{"id":"MP:0000358","label":"abnormal cell morphology"}]}},{"entity":"MGI:2388594","phenotype":{"types":[{"id":"MP:0006288","label":"small otic capsule"}]}},{"entity":"ClinVarVariant:13172","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:2814","phenotype":{"types":[{"id":"HP:0002435","label":"Meningocele"}]}},{"entity":"ClinVarVariant:49939","phenotype":{"types":[{"id":"HP:0009719","label":"Hypomelanotic macule"}]}},{"entity":"ClinVarVariant:101372","phenotype":{"types":[{"id":"HP:0006323","label":"Premature loss of primary teeth"}]}},{"entity":"ZFIN:ZDB-ALT-121112-2","phenotype":{"types":[{"id":"ZP:0017910","label":"abnormal(ly) disrupted amino-acid betaine transport"}]}},{"entity":"ClinVarVariant:215774","phenotype":{"types":[{"id":"HP:0010743","label":"Short metatarsal"}]}},{"entity":"ClinVarVariant:13713","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:24452","phenotype":{"types":[{"id":"HP:0008619","label":"Bilateral sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:5424","phenotype":{"types":[{"id":"HP:0005222","label":"Bowel diverticulosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001398-WBRNAi00027267","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"MGI:3698412","phenotype":{"types":[{"id":"MP:0008713","label":"abnormal cytokine level"}]}},{"entity":"ClinVarVariant:10706","phenotype":{"types":[{"id":"HP:0002023","label":"Anal atresia"}]}},{"entity":"ClinVarVariant:24666","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"ClinVarVariant:181711","phenotype":{"types":[{"id":"HP:0009765","label":"Low hanging columella"}]}},{"entity":"AQTL:48427","phenotype":{"types":[{"id":"AQTLTrait:1067","label":"Length of productive life"}]}},{"entity":"ClinVarVariant:101259","phenotype":{"types":[{"id":"HP:0000015","label":"Bladder diverticulum"}]}},{"entity":"ClinVarVariant:94681","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"FlyBase:FBal0137126","phenotype":{"types":[{"id":"FBbt:00005200PHENOTYPE","label":"denticle phenotype"}]}},{"entity":"ClinVarVariant:25340","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"ClinVarVariant:6066","phenotype":{"types":[{"id":"HP:0009777","label":"Absent thumb"}]}},{"entity":"ClinVarVariant:54024","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1303","phenotype":{"types":[{"id":"ZP:0000719","label":"abnormal(ly) non-contractile heart"}]}},{"entity":"ClinVarVariant:185817","phenotype":{"types":[{"id":"HP:0002076","label":"Migraine"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1164","phenotype":{"types":[{"id":"ZP:0005400","label":"abnormal(ly) hypoplastic horizontal myoseptum"}]}},{"entity":"ClinVarVariant:30939","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"ClinVarVariant:159249","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:53933","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:67868","phenotype":{"types":[{"id":"HP:0004756","label":"Ventricular tachycardia"}]}},{"entity":"MGI:3525250","phenotype":{"types":[{"id":"MP:0004754","label":"abnormal kidney collecting duct morphology"}]}},{"entity":"ClinVarVariant:42086","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"MGI:3050763","phenotype":{"types":[{"id":"HP:0002180","label":"Neurodegeneration"}]}},{"entity":"ClinVarVariant:7185","phenotype":{"types":[{"id":"HP:0001081","label":"Cholelithiasis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007784-WBRNAi00080092","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:24438","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:194417","phenotype":{"types":[{"id":"HP:0000846","label":"Adrenal insufficiency"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022027-WBRNAi00004763","phenotype":{"types":[{"id":"WBPhenotype:0000644","label":"paralyzed"}]}},{"entity":"ClinVarVariant:159660","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:17484","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"MGI:2183933","phenotype":{"types":[{"id":"MP:0004852","label":"decreased testis weight"}]}},{"entity":"ClinVarVariant:24478","phenotype":{"types":[{"id":"HP:0000517","label":"Abnormality of the lens"}]}},{"entity":"MGI:5440173","phenotype":{"types":[{"id":"HP:0000902","label":"Rib fusion"}]}},{"entity":"ClinVarVariant:186923","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"FlyBase:FBal0242627","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"dbSNP:rs10172646","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:2178057","phenotype":{"types":[{"id":"MP:0001360","label":"abnormal social investigation"}]}},{"entity":"ClinVarVariant:9589","phenotype":{"types":[{"id":"HP:0002352","label":"Leukoencephalopathy"}]}},{"entity":"ClinVarVariant:97524","phenotype":{"types":[{"id":"HP:0000999","label":"Pyoderma"}]}},{"entity":"ClinVarVariant:7411","phenotype":{"types":[{"id":"HP:0001100","label":"Heterochromia iridis"}]}},{"entity":"ClinVarVariant:2218","phenotype":{"types":[{"id":"HP:0100544","label":"Neoplasm of the heart"}]}},{"entity":"FlyBase:FBal0042579","phenotype":{"types":[{"id":"FBcv:0002033","label":"lethal - all die during embryonic stage"}]}},{"entity":"ClinVarVariant:68556","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:5051","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"FlyBase:FBal0284394","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"WormBase:WBVar00089606","phenotype":{"types":[{"id":"WBPhenotype:0000565","label":"coiler"}]}},{"entity":"MGI:2386742","phenotype":{"types":[{"id":"MP:0002834","label":"decreased heart weight"}]}},{"entity":"ClinVarVariant:181956","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"dbSNP:rs1819084","phenotype":{"types":[{"id":"HP:0004798","label":"Recurrent infection of the gastrointestinal tract"}]}},{"entity":"ClinVarVariant:40052","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"ClinVarVariant:120250","phenotype":{"types":[{"id":"HP:0002144","label":"Tethered cord"}]}},{"entity":"ClinVarVariant:53360","phenotype":{"types":[{"id":"HP:0000027","label":"Azoospermia"}]}},{"entity":"MGI:3763247","phenotype":{"types":[{"id":"MP:0002376","label":"abnormal dendritic cell physiology"}]}},{"entity":"dbSNP:rs109025111","phenotype":{"types":[{"id":"AQTLTrait:1153","label":"Stillbirth"}]}},{"entity":"ClinVarVariant:67013","phenotype":{"types":[{"id":"HP:0010536","label":"Central sleep apnea"}]}},{"entity":"ClinVarVariant:4765","phenotype":{"types":[{"id":"HP:0000232","label":"Everted lower lip vermilion"}]}},{"entity":"ClinVarVariant:18242","phenotype":{"types":[{"id":"HP:0009919","label":"Retinoblastoma"}]}},{"entity":"ClinVarVariant:215698","phenotype":{"types":[{"id":"HP:0003468","label":"Abnormality of the vertebrae"}]}},{"entity":"ClinVarVariant:24370","phenotype":{"types":[{"id":"HP:0011508","label":"Macular hole"}]}},{"entity":"ClinVarVariant:11043","phenotype":{"types":[{"id":"HP:0001598","label":"Concave nail"}]}},{"entity":"ClinVarVariant:56602","phenotype":{"types":[{"id":"HP:0007738","label":"Uncontrolled eye movements"}]}},{"entity":"MGI:3811777","phenotype":{"types":[{"id":"MP:0001473","label":"reduced long term potentiation"}]}},{"entity":"ClinVarVariant:7235","phenotype":{"types":[{"id":"HP:0100582","label":"Nasal polyposis"}]}},{"entity":"ClinVarVariant:204077","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:127701","phenotype":{"types":[{"id":"HP:0008204","label":"Precocious puberty with Sertoli cell tumor"}]}},{"entity":"MGI:3513454","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:56677","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"ClinVarVariant:210434","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:66491","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"FlyBase:FBal0208645","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:144065","phenotype":{"types":[{"id":"HP:0011484","label":"Posterior synechiae of the anterior chamber"}]}},{"entity":"ClinVarVariant:3914","phenotype":{"types":[{"id":"HP:0003495","label":"GM2-ganglioside accumulation"}]}},{"entity":"ClinVarVariant:1907","phenotype":{"types":[{"id":"HP:0002416","label":"Subependymal cysts"}]}},{"entity":"FlyBase:FBal0097024","phenotype":{"types":[{"id":"FBbt:00001849PHENOTYPE","label":"hypostomal sclerite phenotype"}]}},{"entity":"MGI:2652160","phenotype":{"types":[{"id":"MP:0002452","label":"abnormal professional antigen presenting cell physiology"}]}},{"entity":"MGI:1926453","phenotype":{"types":[{"id":"MP:0003704","label":"abnormal hair follicle development"}]}},{"entity":"ClinVarVariant:6272","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"FlyBase:FBal0296336","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:65525","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"MGI:1861040","phenotype":{"types":[{"id":"MP:0002389","label":"abnormal Peyer's patch follicle morphology"}]}},{"entity":"ClinVarVariant:3491","phenotype":{"types":[{"id":"HP:0003774","label":"Stage 5 chronic kidney disease"}]}},{"entity":"ClinVarVariant:140916","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:95085","phenotype":{"types":[{"id":"HP:0000954","label":"Single transverse palmar crease"}]}},{"entity":"ClinVarVariant:1470","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:189700","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:35858","phenotype":{"types":[{"id":"HP:0006516","label":"Hypersensitivity pneumonitis"}]}},{"entity":"MGI:2389582","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:135777","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"MGI:2429736","phenotype":{"types":[{"id":"MP:0010776","label":"abnormal placenta metrial gland morphology"}]}},{"entity":"ClinVarVariant:6652","phenotype":{"types":[{"id":"HP:0003741","label":"Congenital muscular dystrophy"}]}},{"entity":"ClinVarVariant:204093","phenotype":{"types":[{"id":"HP:0000112","label":"Nephropathy"}]}},{"entity":"ClinVarVariant:132711","phenotype":{"types":[{"id":"HP:0000706","label":"Unerupted tooth"}]}},{"entity":"_:genid1976000","phenotype":{"types":[{"id":"ZP:0000765","label":"abnormal(ly) increased size optic tectum"}]}},{"entity":"ClinVarVariant:188879","phenotype":{"types":[{"id":"HP:0200032","label":"Kayser-Fleischer ring"}]}},{"entity":"ClinVarVariant:5279","phenotype":{"types":[{"id":"HP:0010978","label":"Abnormality of immune system physiology"}]}},{"entity":"ClinVarVariant:136102","phenotype":{"types":[{"id":"HP:0010829","label":"Impaired temperature sensation"}]}},{"entity":"ClinVarVariant:11456","phenotype":{"types":[{"id":"HP:0000679","label":"Taurodontia"}]}},{"entity":"MGI:5471642","phenotype":{"types":[{"id":"MP:0006042","label":"increased apoptosis"}]}},{"entity":"ClinVarVariant:42357","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"ClinVarVariant:40245","phenotype":{"types":[{"id":"HP:0100775","label":"Dural ectasia"}]}},{"entity":"ClinVarVariant:188801","phenotype":{"types":[{"id":"HP:0001933","label":"Subcutaneous hemorrhage"}]}},{"entity":"ClinVarVariant:180636","phenotype":{"types":[{"id":"HP:0001339","label":"Lissencephaly"}]}},{"entity":"ClinVarVariant:31017","phenotype":{"types":[{"id":"HP:0006439","label":"Radioulnar dislocation"}]}},{"entity":"ClinVarVariant:38932","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:13997","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:155793","phenotype":{"types":[{"id":"HP:0001646","label":"Abnormality of the aortic valve"}]}},{"entity":"ClinVarVariant:10108","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"ClinVarVariant:17346","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"MGI:5297423","phenotype":{"types":[{"id":"HP:0011641","label":"Coronary artery fistula"}]}},{"entity":"dbSNP:rs80934742","phenotype":{"types":[{"id":"AQTLTrait:1181","label":"Muscle pH"}]}},{"entity":"ClinVarVariant:49414","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"NCBIGene:105463128","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"ClinVarVariant:36381","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:1529","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:1087","phenotype":{"types":[{"id":"HP:0001371","label":"Flexion contracture"}]}},{"entity":"ClinVarVariant:184154","phenotype":{"types":[{"id":"HP:0001920","label":"Renal artery stenosis"}]}},{"entity":"FlyBase:FBal0127293","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:67926","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:3961","phenotype":{"types":[{"id":"HP:0000652","label":"Lower eyelid coloboma"}]}},{"entity":"ClinVarVariant:40983","phenotype":{"types":[{"id":"HP:0003025","label":"Metaphyseal irregularity"}]}},{"entity":"ClinVarVariant:3282","phenotype":{"types":[{"id":"HP:0010302","label":"Spinal cord tumor"}]}},{"entity":"ClinVarVariant:1825","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:1115","phenotype":{"types":[{"id":"HP:0000608","label":"Macular degeneration"}]}},{"entity":"ClinVarVariant:25059","phenotype":{"types":[{"id":"HP:0100275","label":"Diffuse cerebellar atrophy"}]}},{"entity":"ClinVarVariant:197758","phenotype":{"types":[{"id":"HP:0001685","label":"Myocardial fibrosis"}]}},{"entity":"ClinVarVariant:210424","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000390-WBRNAi00034721","phenotype":{"types":[{"id":"WBPhenotype:0000700","label":"multivulva"}]}},{"entity":"ClinVarVariant:8953","phenotype":{"types":[{"id":"HP:0000126","label":"Hydronephrosis"}]}},{"entity":"FlyBase:FBal0200755","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:100775","phenotype":{"types":[{"id":"HP:0001371","label":"Flexion contracture"}]}},{"entity":"ClinVarVariant:8746","phenotype":{"types":[{"id":"HP:0009908","label":"Anterior creases of earlobe"}]}},{"entity":"ClinVarVariant:53456","phenotype":{"types":[{"id":"HP:0006538","label":"Recurrent bronchopulmonary infections"}]}},{"entity":"ClinVarVariant:216771","phenotype":{"types":[{"id":"HP:0002385","label":"Paraparesis"}]}},{"entity":"ZFIN:ZDB-ALT-150115-1","phenotype":{"types":[{"id":"ZP:0013924","label":"abnormal(ly) has fewer parts of type spinal cord motor neuron towards motor neuron synapse"}]}},{"entity":"ClinVarVariant:12483","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"ClinVarVariant:41057","phenotype":{"types":[{"id":"HP:0010297","label":"Bifid tongue"}]}},{"entity":"ClinVarVariant:24459","phenotype":{"types":[{"id":"HP:0100273","label":"Neoplasm of the colon"}]}},{"entity":"ClinVarVariant:41112","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:17292","phenotype":{"types":[{"id":"HP:0001518","label":"Small for gestational age"}]}},{"entity":"ClinVarVariant:11826","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"MGI:3526854","phenotype":{"types":[{"id":"MP:0010587","label":"conotruncal ridge hypoplasia"}]}},{"entity":"ClinVarVariant:4024","phenotype":{"types":[{"id":"HP:0000158","label":"Macroglossia"}]}},{"entity":"ClinVarVariant:126402","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:53518","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"NCBIGene:46","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:25235","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"FlyBase:FBal0208051","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:31215","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"MGI:3702579","phenotype":{"types":[{"id":"HP:0005403","label":"T lymphocytopenia"}]}},{"entity":"FlyBase:FBal0042742","phenotype":{"types":[{"id":"FBcv:0002041","label":"some die during embryonic stage"}]}},{"entity":"NCBIGene:2759","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"dbSNP:rs43015698","phenotype":{"types":[{"id":"AQTLTrait:1327","label":"Milk odd-chain fatty acid percentage"}]}},{"entity":"ClinVarVariant:13664","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:101165","phenotype":{"types":[{"id":"HP:0100645","label":"Cystocele"}]}},{"entity":"ClinVarVariant:120291","phenotype":{"types":[{"id":"HP:0001992","label":"Organic aciduria"}]}},{"entity":"ClinVarVariant:10888","phenotype":{"types":[{"id":"HP:0000496","label":"Abnormality of eye movement"}]}},{"entity":"ClinVarVariant:12783","phenotype":{"types":[{"id":"HP:0002668","label":"Paraganglioma"}]}},{"entity":"ClinVarVariant:189202","phenotype":{"types":[{"id":"HP:0001662","label":"Bradycardia"}]}},{"entity":"ClinVarVariant:1114","phenotype":{"types":[{"id":"HP:0001258","label":"Spastic paraplegia"}]}},{"entity":"ClinVarVariant:53933","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:49975","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"MGI:3692444","phenotype":{"types":[{"id":"MP:0011089","label":"perinatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:53448","phenotype":{"types":[{"id":"HP:0100646","label":"Thyroiditis"}]}},{"entity":"ClinVarVariant:101175","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:188802","phenotype":{"types":[{"id":"HP:0100022","label":"Abnormality of movement"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-070206-1-ZDB-MRPHLNO-120719-3","phenotype":{"types":[{"id":"ZP:0003863","label":"abnormal(ly) malformed caudal vein plexus"}]}},{"entity":"FlyBase:FBal0267174","phenotype":{"types":[{"id":"FBcv:0000425","label":"increased cell death"}]}},{"entity":"ClinVarVariant:159086","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:41388","phenotype":{"types":[{"id":"HP:0008069","label":"Neoplasm of the skin"}]}},{"entity":"ClinVarVariant:132731","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:132873","phenotype":{"types":[{"id":"HP:0005059","label":"Arthralgia/arthritis"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-040704-56-ZDB-MRPHLNO-150717-3","phenotype":{"types":[{"id":"GO:0001654PHENOTYPE","label":"eye development phenotype"}]}},{"entity":"dbSNP:rs135873847","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"MGI:1856333","phenotype":{"types":[{"id":"MP:0008917","label":"abnormal oligodendrocyte physiology"}]}},{"entity":"ClinVarVariant:21109","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:95186","phenotype":{"types":[{"id":"HP:0002793","label":"Abnormal pattern of respiration"}]}},{"entity":"ClinVarVariant:2931","phenotype":{"types":[{"id":"HP:0010628","label":"Facial palsy"}]}},{"entity":"FlyBase:FBal0206992","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:53489","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:54034","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"MGI:1926453","phenotype":{"types":[{"id":"MP:0000424","label":"retarded hair growth"}]}},{"entity":"MGI:3577203","phenotype":{"types":[{"id":"MP:0006082","label":"CNS inflammation"}]}},{"entity":"ClinVarVariant:162523","phenotype":{"types":[{"id":"HP:0010055","label":"Broad hallux"}]}},{"entity":"dbSNP:rs1864400","phenotype":{"types":[{"id":"HP:0004401","label":"Meconium ileus"}]}},{"entity":"ClinVarVariant:50259","phenotype":{"types":[{"id":"HP:0002756","label":"Pathologic fracture"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000063-WBRNAi00026183","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"_:genid1974640","phenotype":{"types":[{"id":"ZP:0001504","label":"abnormal(ly) present in fewer numbers in organism myotome skeletal muscle cell"}]}},{"entity":"ClinVarVariant:91660","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:215589","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:102846","phenotype":{"types":[{"id":"HP:0003231","label":"Hypertyrosinemia"}]}},{"entity":"ClinVarVariant:30013","phenotype":{"types":[{"id":"HP:0000294","label":"Low anterior hairline"}]}},{"entity":"ClinVarVariant:10664","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"MGI:3693248","phenotype":{"types":[{"id":"GO:0008016PHENOTYPE","label":"regulation of heart contraction phenotype"}]}},{"entity":"FlyBase:FBal0246629","phenotype":{"types":[{"id":"GO:0030054PHENOTYPE","label":"cell junction phenotype"}]}},{"entity":"MGI:2179534","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"MGI:3689957","phenotype":{"types":[{"id":"MP:0010205","label":"abnormal oligodendrocyte apoptosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007352-WBRNAi00079985","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011747-WBRNAi00073828","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:53610","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:10551","phenotype":{"types":[{"id":"HP:0000597","label":"Ophthalmoparesis"}]}},{"entity":"ClinVarVariant:53330","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:10318","phenotype":{"types":[{"id":"HP:0100614","label":"Myositis"}]}},{"entity":"ClinVarVariant:10063","phenotype":{"types":[{"id":"HP:0007325","label":"Generalized dystonia"}]}},{"entity":"MGI:2183949","phenotype":{"types":[{"id":"HP:0011902","label":"Abnormal hemoglobin"}]}},{"entity":"ClinVarVariant:10736","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"ClinVarVariant:24650","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:177834","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"MGI:3701835","phenotype":{"types":[{"id":"HP:0003687","label":"Centrally nucleated skeletal muscle fibers"}]}},{"entity":"ClinVarVariant:11520","phenotype":{"types":[{"id":"HP:0002007","label":"Frontal bossing"}]}},{"entity":"ClinVarVariant:17491","phenotype":{"types":[{"id":"HP:0000360","label":"Tinnitus"}]}},{"entity":"ClinVarVariant:7445","phenotype":{"types":[{"id":"HP:0100896","label":"Rectal polyposis"}]}},{"entity":"ClinVarVariant:161357","phenotype":{"types":[{"id":"HP:0001166","label":"Arachnodactyly"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004453-WBRNAi00085642","phenotype":{"types":[{"id":"WBPhenotype:0000291","label":"no oocytes"}]}},{"entity":"MGI:2181662","phenotype":{"types":[{"id":"MP:0008515","label":"thin retinal outer nuclear layer"}]}},{"entity":"_:genid1975883","phenotype":{"types":[{"id":"ZP:0000319","label":"abnormal(ly) hydrocephalic brain"}]}},{"entity":"ClinVarVariant:7519","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"MGI:3655845","phenotype":{"types":[{"id":"HP:0007033","label":"Cerebellar dysplasia"}]}},{"entity":"ClinVarVariant:12038","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"_:genid1938554","phenotype":{"types":[{"id":"ZP:0000473","label":"abnormal(ly) decreased length whole organism"}]}},{"entity":"ClinVarVariant:162387","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"MGI:3830289","phenotype":{"types":[{"id":"HP:0001669","label":"Transposition of the great arteries"}]}},{"entity":"dbSNP:rs1953600","phenotype":{"types":[{"id":"HP:0006516","label":"Hypersensitivity pneumonitis"}]}},{"entity":"FlyBase:FBal0199757","phenotype":{"types":[{"id":"FBbt:00004580PHENOTYPE","label":"Drosophila mesothoracic tergum phenotype"}]}},{"entity":"ClinVarVariant:204228","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:1901","phenotype":{"types":[{"id":"HP:0007360","label":"Aplasia/Hypoplasia of the cerebellum"}]}},{"entity":"ClinVarVariant:101364","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"MGI:5641735","phenotype":{"types":[{"id":"MP:0000877","label":"abnormal Purkinje cell morphology"}]}},{"entity":"ClinVarVariant:35895","phenotype":{"types":[{"id":"HP:0006706","label":"Cystic liver disease"}]}},{"entity":"ClinVarVariant:8733","phenotype":{"types":[{"id":"HP:0003128","label":"Lactic acidosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003073-WBRNAi00034975","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:11667","phenotype":{"types":[{"id":"HP:0001187","label":"Hyperextensibility of the finger joints"}]}},{"entity":"FlyBase:FBal0197891","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:143534","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"ClinVarVariant:41696","phenotype":{"types":[{"id":"HP:0009734","label":"Optic glioma"}]}},{"entity":"ClinVarVariant:64974","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:7440","phenotype":{"types":[{"id":"HP:0000069","label":"Abnormality of the ureter"}]}},{"entity":"dbSNP:rs43703486","phenotype":{"types":[{"id":"AQTLTrait:1096","label":"Teat length"}]}},{"entity":"ClinVarVariant:13351","phenotype":{"types":[{"id":"HP:0000391","label":"Thickened helices"}]}},{"entity":"ClinVarVariant:65898","phenotype":{"types":[{"id":"HP:0000939","label":"Osteoporosis"}]}},{"entity":"ClinVarVariant:10068","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"WormBase:WBVar00088666","phenotype":{"types":[{"id":"WBPhenotype:0000012","label":"dauer constitutive"}]}},{"entity":"ClinVarVariant:56031","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:5559","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"MGI:2176775","phenotype":{"types":[{"id":"MP:0002169","label":"no abnormal phenotype detected"}]}},{"entity":"ClinVarVariant:782","phenotype":{"types":[{"id":"HP:0003201","label":"Rhabdomyolysis"}]}},{"entity":"WormBase:WBVar00088241","phenotype":{"types":[{"id":"WBPhenotype:0001351","label":"protein phosphorylation reduced"}]}},{"entity":"ClinVarVariant:42327","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"ClinVarVariant:217027","phenotype":{"types":[{"id":"HP:0000682","label":"Abnormality of dental enamel"}]}},{"entity":"ClinVarVariant:38314","phenotype":{"types":[{"id":"HP:0000046","label":"Scrotal hypoplasia"}]}},{"entity":"ClinVarVariant:7926","phenotype":{"types":[{"id":"HP:0007856","label":"Punctate opacification of the cornea"}]}},{"entity":"ClinVarVariant:53670","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:101202","phenotype":{"types":[{"id":"HP:0005267","label":"Premature delivery because of cervical insufficiency or membrane fragility"}]}},{"entity":"MGI:2450853","phenotype":{"types":[{"id":"HP:0000798","label":"Oligospermia"}]}},{"entity":"ClinVarVariant:136171","phenotype":{"types":[{"id":"HP:0002044","label":"Zollinger-Ellison syndrome"}]}},{"entity":"ClinVarVariant:210444","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:38425","phenotype":{"types":[{"id":"HP:0003264","label":"Deficiency of N-acetylglucosamine-1-phosphotransferase"}]}},{"entity":"ClinVarVariant:96","phenotype":{"types":[{"id":"HP:0000153","label":"Abnormality of the mouth"}]}},{"entity":"ClinVarVariant:24380","phenotype":{"types":[{"id":"HP:0100242","label":"Sarcoma"}]}},{"entity":"ClinVarVariant:7789","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"MGI:2667333","phenotype":{"types":[{"id":"HP:0002733","label":"Abnormality of the lymph nodes"}]}},{"entity":"ClinVarVariant:5590","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:209077","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:2116","phenotype":{"types":[{"id":"HP:0002510","label":"Spastic tetraplegia"}]}},{"entity":"ClinVarVariant:208182","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:54093","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:982","phenotype":{"types":[{"id":"HP:0005105","label":"Abnormal nasal morphology"}]}},{"entity":"ClinVarVariant:39785","phenotype":{"types":[{"id":"HP:0000592","label":"Blue sclerae"}]}},{"entity":"ClinVarVariant:41202","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:11096","phenotype":{"types":[{"id":"HP:0010307","label":"Stridor"}]}},{"entity":"ClinVarVariant:192241","phenotype":{"types":[{"id":"HP:0000734","label":"Disinhibition"}]}},{"entity":"ClinVarVariant:50030","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"dbSNP:rs1953600","phenotype":{"types":[{"id":"HP:0011134","label":"Low-grade fever"}]}},{"entity":"MGI:2678819","phenotype":{"types":[{"id":"MP:0008083","label":"decreased single-positive T cell number"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00044800-WBRNAi00085802","phenotype":{"types":[{"id":"WBPhenotype:0000186","label":"oogenesis variant"}]}},{"entity":"MGI:5293082","phenotype":{"types":[{"id":"HP:0002910","label":"Elevated hepatic transaminases"}]}},{"entity":"ClinVarVariant:209047","phenotype":{"types":[{"id":"HP:0002331","label":"Headache (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:13349","phenotype":{"types":[{"id":"HP:0000465","label":"Webbed neck"}]}},{"entity":"ClinVarVariant:16262","phenotype":{"types":[{"id":"HP:0003759","label":"Hypoplasia of lymphatic vessels"}]}},{"entity":"ClinVarVariant:4320","phenotype":{"types":[{"id":"HP:0003540","label":"Impaired platelet aggregation"}]}},{"entity":"ClinVarVariant:137948","phenotype":{"types":[{"id":"HP:0000768","label":"Pectus carinatum"}]}},{"entity":"ClinVarVariant:11124","phenotype":{"types":[{"id":"HP:0001891","label":"Iron deficiency anemia"}]}},{"entity":"ClinVarVariant:212207","phenotype":{"types":[{"id":"HP:0002015","label":"Dysphagia"}]}},{"entity":"ClinVarVariant:5194","phenotype":{"types":[{"id":"HP:0002694","label":"Sclerosis of skull base"}]}},{"entity":"ClinVarVariant:65750","phenotype":{"types":[{"id":"HP:0001875","label":"Neutropenia"}]}},{"entity":"ClinVarVariant:3843","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:279","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"ClinVarVariant:65513","phenotype":{"types":[{"id":"HP:0000546","label":"Retinal degeneration"}]}},{"entity":"ClinVarVariant:2146","phenotype":{"types":[{"id":"HP:0001377","label":"Limited elbow extension"}]}},{"entity":"FlyBase:FBal0175418","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"FlyBase:FBal0203926","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:208026","phenotype":{"types":[{"id":"HP:0000280","label":"Coarse facial features"}]}},{"entity":"ClinVarVariant:10232","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"ClinVarVariant:200129","phenotype":{"types":[{"id":"HP:0004937","label":"Pulmonary artery aneurysm"}]}},{"entity":"ClinVarVariant:53494","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:5069","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:5145","phenotype":{"types":[{"id":"HP:0008625","label":"Severe sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:40594","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ZFIN:ZDB-ALT-060301-2","phenotype":{"types":[{"id":"ZP:0012481","label":"abnormal(ly) decreased cellular motility branchiomotor neuron"}]}},{"entity":"ClinVarVariant:6292","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:24279","phenotype":{"types":[{"id":"HP:0000613","label":"Photophobia"}]}},{"entity":"ClinVarVariant:10765","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"MGI:3689422","phenotype":{"types":[{"id":"MP:0008302","label":"thin adrenal cortex"}]}},{"entity":"MGI:2387343","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"MGI:3056733","phenotype":{"types":[{"id":"MP:0009820","label":"abnormal liver vasculature morphology"}]}},{"entity":"ClinVarVariant:7215","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:92592","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"MGI:3810526","phenotype":{"types":[{"id":"HP:0005404","label":"Increase in B cell number"}]}},{"entity":"ClinVarVariant:190250","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:215683","phenotype":{"types":[{"id":"HP:0100246","label":"Osteoma"}]}},{"entity":"ClinVarVariant:14924","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:72","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"FlyBase:FBal0262639","phenotype":{"types":[{"id":"FBbt:00000052PHENOTYPE","label":"Drosophila embryo phenotype"}]}},{"entity":"FlyBase:FBal0104352","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"FlyBase:FBal0125070","phenotype":{"types":[{"id":"FBbt:00004511PHENOTYPE","label":"Drosophila antenna phenotype"}]}},{"entity":"MGI:1856555","phenotype":{"types":[{"id":"MP:0004528","label":"fused outer hair cell stereocilia"}]}},{"entity":"ClinVarVariant:132644","phenotype":{"types":[{"id":"HP:0003108","label":"Hyperglycinuria"}]}},{"entity":"ClinVarVariant:67509","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"MGI:5507843","phenotype":{"types":[{"id":"MP:0002084","label":"abnormal developmental patterning"}]}},{"entity":"ClinVarVariant:183434","phenotype":{"types":[{"id":"HP:0000358","label":"Posteriorly rotated ears"}]}},{"entity":"MGI:2183515","phenotype":{"types":[{"id":"MP:0011100","label":"preweaning lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:36320","phenotype":{"types":[{"id":"HP:0011906","label":"Reduced beta/alpha synthesis ratio"}]}},{"entity":"ClinVarVariant:10859","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"AQTL:54067","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:13351","phenotype":{"types":[{"id":"HP:0010935","label":"Abnormality of the upper urinary tract"}]}},{"entity":"ClinVarVariant:158279","phenotype":{"types":[{"id":"HP:0006191","label":"Deep palmar crease"}]}},{"entity":"ClinVarVariant:41145","phenotype":{"types":[{"id":"HP:0000286","label":"Epicanthus"}]}},{"entity":"ClinVarVariant:185834","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:1856328","phenotype":{"types":[{"id":"MP:0013237","label":"abnormal skeletal muscle regeneration"}]}},{"entity":"ClinVarVariant:217049","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:12690","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:13949","phenotype":{"types":[{"id":"HP:0000843","label":"Hyperparathyroidism"}]}},{"entity":"MGI:1856197","phenotype":{"types":[{"id":"MP:0006371","label":"absent hair follicle pheomelanosome pheomelanin"}]}},{"entity":"ClinVarVariant:53229","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"ClinVarVariant:143582","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:210446","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"ClinVarVariant:10146","phenotype":{"types":[{"id":"HP:0005261","label":"Joint hemorrhage"}]}},{"entity":"ClinVarVariant:54044","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"MGI:1856009","phenotype":{"types":[{"id":"HP:0000855","label":"Insulin resistance"}]}},{"entity":"ClinVarVariant:40680","phenotype":{"types":[{"id":"HP:0001595","label":"Abnormality of the hair"}]}},{"entity":"ClinVarVariant:167487","phenotype":{"types":[{"id":"HP:0005576","label":"Tubulointerstitial fibrosis"}]}},{"entity":"ClinVarVariant:17322","phenotype":{"types":[{"id":"HP:0002659","label":"Increased susceptibility to fractures"}]}},{"entity":"ClinVarVariant:8212","phenotype":{"types":[{"id":"HP:0100730","label":"Bronchogenic cyst"}]}},{"entity":"ClinVarVariant:156529","phenotype":{"types":[{"id":"HP:0011950","label":"Bronchiolitis"}]}},{"entity":"ClinVarVariant:210464","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:159157","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"ClinVarVariant:25225","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"MGI:1889570","phenotype":{"types":[{"id":"GO:0006112PHENOTYPE","label":"energy reserve metabolic process phenotype"}]}},{"entity":"ClinVarVariant:53366","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:167138","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:30835","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"NCBIGene:100188340","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:906","phenotype":{"types":[{"id":"HP:0002721","label":"Immunodeficiency"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-991124-7-ZDB-MRPHLNO-060328-3","phenotype":{"types":[{"id":"ZP:0008625","label":"abnormal(ly) physical object quality pectoral fin"}]}},{"entity":"MGI:2182273","phenotype":{"types":[{"id":"HP:0005403","label":"T lymphocytopenia"}]}},{"entity":"ClinVarVariant:2712","phenotype":{"types":[{"id":"HP:0000268","label":"Dolichocephaly"}]}},{"entity":"ClinVarVariant:1655","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:49520","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:159216","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:180362","phenotype":{"types":[{"id":"HP:0000166","label":"Severe periodontitis"}]}},{"entity":"ClinVarVariant:2687","phenotype":{"types":[{"id":"HP:0001297","label":"Stroke"}]}},{"entity":"ClinVarVariant:41224","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ClinVarVariant:190257","phenotype":{"types":[{"id":"HP:0100646","label":"Thyroiditis"}]}},{"entity":"ClinVarVariant:4364","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"ClinVarVariant:143482","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:36962","phenotype":{"types":[{"id":"HP:0002652","label":"Skeletal dysplasia"}]}},{"entity":"ClinVarVariant:65377","phenotype":{"types":[{"id":"HP:0009734","label":"Optic glioma"}]}},{"entity":"FlyBase:FBal0051183","phenotype":{"types":[{"id":"FBcv:0002000","label":"lethal - all die before end of P-stage"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050208-123-ZDB-MRPHLNO-150410-1-ZDB-MRPHLNO-150424-1","phenotype":{"types":[{"id":"ZP:0001849","label":"abnormal(ly) present in greater numbers in organism pronephros multi-ciliated epithelial cell"}]}},{"entity":"ClinVarVariant:103","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:6619","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"AQTL:44271","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:40555","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:12483","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"ClinVarVariant:41882","phenotype":{"types":[{"id":"HP:0001321","label":"Cerebellar hypoplasia"}]}},{"entity":"ClinVarVariant:42347","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"MGI:2384332","phenotype":{"types":[{"id":"MP:0003921","label":"abnormal heart left ventricle morphology"}]}},{"entity":"ClinVarVariant:53206","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:24468","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:16424","phenotype":{"types":[{"id":"HP:0100749","label":"Chest pain"}]}},{"entity":"ClinVarVariant:16875","phenotype":{"types":[{"id":"HP:0003325","label":"Limb-girdle muscle weakness"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-030127-1-ZDB-MRPHLNO-051221-6","phenotype":{"types":[{"id":"ZP:0000132","label":"abnormal(ly) malformed ceratohyal cartilage"}]}},{"entity":"ClinVarVariant:53974","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:53710","phenotype":{"types":[{"id":"HP:0011892","label":"Vitamin K deficiency"}]}},{"entity":"ClinVarVariant:142434","phenotype":{"types":[{"id":"HP:0002073","label":"Progressive cerebellar ataxia"}]}},{"entity":"ClinVarVariant:13055","phenotype":{"types":[{"id":"HP:0001123","label":"Visual field defect"}]}},{"entity":"ClinVarVariant:24782","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:157934","phenotype":{"types":[{"id":"HP:0001433","label":"Hepatosplenomegaly"}]}},{"entity":"MGI:2150685","phenotype":{"types":[{"id":"MP:0004616","label":"lumbar vertebral transformation"}]}},{"entity":"ClinVarVariant:11962","phenotype":{"types":[{"id":"HP:0000090","label":"Nephronophthisis"}]}},{"entity":"ClinVarVariant:13394","phenotype":{"types":[{"id":"HP:0002381","label":"Aphasia"}]}},{"entity":"MGI:3574394","phenotype":{"types":[{"id":"HP:0005180","label":"Tricuspid regurgitation"}]}},{"entity":"ClinVarVariant:13369","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"AQTL:23249","phenotype":{"types":[{"id":"AQTLTrait:1252","label":"Milk myristic acid percentage"}]}},{"entity":"ClinVarVariant:42400","phenotype":{"types":[{"id":"HP:0000646","label":"Amblyopia"}]}},{"entity":"ClinVarVariant:5540","phenotype":{"types":[{"id":"HP:0100726","label":"Kaposi's sarcoma"}]}},{"entity":"MGI:3576366","phenotype":{"types":[{"id":"MP:0009503","label":"abnormal mammary gland duct morphology"}]}},{"entity":"ClinVarVariant:143094","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"ClinVarVariant:48927","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"MGI:3580645","phenotype":{"types":[{"id":"MP:0009004","label":"progressive hair loss"}]}},{"entity":"ClinVarVariant:142003","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:56607","phenotype":{"types":[{"id":"HP:0004327","label":"Abnormality of the vitreous humor"}]}},{"entity":"ClinVarVariant:136164","phenotype":{"types":[{"id":"HP:0000825","label":"Hyperinsulinemic hypoglycemia"}]}},{"entity":"MGI:2670437","phenotype":{"types":[{"id":"MP:0000886","label":"abnormal cerebellar granule layer morphology"}]}},{"entity":"ClinVarVariant:167723","phenotype":{"types":[{"id":"HP:0002894","label":"Neoplasm of the pancreas"}]}},{"entity":"ClinVarVariant:17344","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:41212","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:209049","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"dbSNP:rs29013986","phenotype":{"types":[{"id":"AQTLTrait:1169","label":"Interval to first estrus after calving"}]}},{"entity":"ClinVarVariant:210454","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"MGI:1857966","phenotype":{"types":[{"id":"HP:0001402","label":"Hepatocellular carcinoma"}]}},{"entity":"ClinVarVariant:56243","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:208006","phenotype":{"types":[{"id":"HP:0002748","label":"Rickets"}]}},{"entity":"ClinVarVariant:139531","phenotype":{"types":[{"id":"HP:0012588","label":"Steroid-resistant nephrotic syndrome"}]}},{"entity":"ClinVarVariant:56191","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:49423","phenotype":{"types":[{"id":"HP:0009734","label":"Optic glioma"}]}},{"entity":"ClinVarVariant:11712","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:53393","phenotype":{"types":[{"id":"HP:0006530","label":"Interstitial pulmonary disease"}]}},{"entity":"FlyBase:FBal0297079","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"FlyBase:FBal0200543","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:92359","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ZFIN:ZDB-ALT-030919-2","phenotype":{"types":[{"id":"ZP:0006939","label":"abnormal(ly) has fewer parts of type spinal cord towards motor neuron"}]}},{"entity":"ClinVarVariant:216475","phenotype":{"types":[{"id":"HP:0100641","label":"Neoplasm of the adrenal cortex"}]}},{"entity":"ClinVarVariant:29874","phenotype":{"types":[{"id":"HP:0000580","label":"Pigmentary retinopathy"}]}},{"entity":"ClinVarVariant:10830","phenotype":{"types":[{"id":"HP:0003502","label":"Mild short stature"}]}},{"entity":"ClinVarVariant:95023","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:195913","phenotype":{"types":[{"id":"HP:0002342","label":"Intellectual disability, moderate"}]}},{"entity":"MGI:2387957","phenotype":{"types":[{"id":"MP:0001501","label":"abnormal sleep pattern"}]}},{"entity":"MGI:2386680","phenotype":{"types":[{"id":"GO:0042127PHENOTYPE","label":"regulation of cell proliferation phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00077732-WBRNAi00085693","phenotype":{"types":[{"id":"WBPhenotype:0001973","label":"germ cell compartment size variant"}]}},{"entity":"ClinVarVariant:135735","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008686-WBRNAi00074140","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:12403","phenotype":{"types":[{"id":"HP:0009720","label":"Adenoma sebaceum"}]}},{"entity":"MGI:5312925","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"FlyBase:FBal0202682","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:9886","phenotype":{"types":[{"id":"HP:0007984","label":"Reduced amplitude of dark-adapted bright flash electroretinogram b-wave"}]}},{"entity":"ClinVarVariant:1147","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:93888","phenotype":{"types":[{"id":"HP:0001558","label":"Decreased fetal movement"}]}},{"entity":"FlyBase:FBal0304813","phenotype":{"types":[{"id":"FBcv:0000366","label":"female sterile"}]}},{"entity":"MGI:1857056","phenotype":{"types":[{"id":"MP:0006396","label":"decreased long bone epiphyseal plate size"}]}},{"entity":"ClinVarVariant:53989","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:49828","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-041116-2-ZDB-MRPHLNO-150216-1-ZDB-MRPHLNO-150216-2","phenotype":{"types":[{"id":"ZP:0012064","label":"abnormal(ly) decreased occurrence adenohypophysis corticotropin hormone secreting cell differentiation"}]}},{"entity":"ClinVarVariant:2679","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"MGI:2671317","phenotype":{"types":[{"id":"MP:0011089","label":"perinatal lethality, complete penetrance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004808-WBRNAi00072509","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:93457","phenotype":{"types":[{"id":"HP:0001873","label":"Thrombocytopenia"}]}},{"entity":"ClinVarVariant:1563","phenotype":{"types":[{"id":"HP:0003309","label":"Ovoid thoracolumbar vertebrae"}]}},{"entity":"ClinVarVariant:159086","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"MGI:4365388","phenotype":{"types":[{"id":"MP:0009793","label":"sebaceous gland hypertrophy"}]}},{"entity":"ClinVarVariant:198219","phenotype":{"types":[{"id":"HP:0000590","label":"Progressive external ophthalmoplegia"}]}},{"entity":"dbSNP:rs110304690","phenotype":{"types":[{"id":"AQTLTrait:1101","label":"Foot angle"}]}},{"entity":"ClinVarVariant:7982","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:7141","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"AQTL:35966","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:9970","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:101176","phenotype":{"types":[{"id":"HP:0000387","label":"Absent earlobe"}]}},{"entity":"ClinVarVariant:162666","phenotype":{"types":[{"id":"HP:0011950","label":"Bronchiolitis"}]}},{"entity":"MGI:1856681","phenotype":{"types":[{"id":"MP:0002855","label":"abnormal cochlear ganglion morphology"}]}},{"entity":"ClinVarVariant:67987","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"MGI:4946645","phenotype":{"types":[{"id":"MP:0000947","label":"convulsive seizures"}]}},{"entity":"ClinVarVariant:4268","phenotype":{"types":[{"id":"HP:0004370","label":"Abnormality of temperature regulation"}]}},{"entity":"ClinVarVariant:11356","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"ClinVarVariant:4439","phenotype":{"types":[{"id":"HP:0002317","label":"Unsteady gait"}]}},{"entity":"ClinVarVariant:11002","phenotype":{"types":[{"id":"HP:0001298","label":"Encephalopathy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002845-WBRNAi00064383","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"ClinVarVariant:132848","phenotype":{"types":[{"id":"HP:0000023","label":"Inguinal hernia"}]}},{"entity":"ClinVarVariant:209057","phenotype":{"types":[{"id":"HP:0002331","label":"Headache (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:10175","phenotype":{"types":[{"id":"HP:0011892","label":"Vitamin K deficiency"}]}},{"entity":"dbSNP:rs29025964","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:49552","phenotype":{"types":[{"id":"HP:0009554","label":"Projection of scalp hair onto lateral cheek"}]}},{"entity":"MGI:3578093","phenotype":{"types":[{"id":"HP:0001978","label":"Extramedullary hematopoiesis"}]}},{"entity":"_:genid1975192","phenotype":{"types":[{"id":"ZP:0004393","label":"abnormal(ly) truncated intersegmental vessel"}]}},{"entity":"ClinVarVariant:17312","phenotype":{"types":[{"id":"HP:0002659","label":"Increased susceptibility to fractures"}]}},{"entity":"ClinVarVariant:10154","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:30150","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:17324","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:216201","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:38497","phenotype":{"types":[{"id":"HP:0002017","label":"Nausea and vomiting"}]}},{"entity":"ClinVarVariant:126384","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"ClinVarVariant:13938","phenotype":{"types":[{"id":"HP:0100835","label":"Benign neoplasm of the central nervous system"}]}},{"entity":"MGI:3623342","phenotype":{"types":[{"id":"MP:0011967","label":"increased or absent threshold for auditory brainstem response"}]}},{"entity":"ClinVarVariant:188826","phenotype":{"types":[{"id":"HP:0002352","label":"Leukoencephalopathy"}]}},{"entity":"ClinVarVariant:11359","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:43167","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"AQTL:43115","phenotype":{"types":[{"id":"AQTLTrait:1112","label":"Withers height"}]}},{"entity":"MGI:5502178","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"ClinVarVariant:24217","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:17314","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:139523","phenotype":{"types":[{"id":"HP:0001480","label":"Freckling"}]}},{"entity":"ClinVarVariant:215634","phenotype":{"types":[{"id":"HP:0001017","label":"Anemic pallor"}]}},{"entity":"ClinVarVariant:210454","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:1535","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:5691","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"NCBIGene:57788","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:10717","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"ClinVarVariant:53820","phenotype":{"types":[{"id":"HP:0100513","label":"Vitamin E deficiency"}]}},{"entity":"ClinVarVariant:189569","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"MGI:3512143","phenotype":{"types":[{"id":"HP:0003468","label":"Abnormality of the vertebrae"}]}},{"entity":"ClinVarVariant:6718","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:9581","phenotype":{"types":[{"id":"HP:0000602","label":"Ophthalmoplegia"}]}},{"entity":"ClinVarVariant:4306","phenotype":{"types":[{"id":"HP:0100787","label":"Prostate neoplasm"}]}},{"entity":"ClinVarVariant:50861","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:3408","phenotype":{"types":[{"id":"HP:0000982","label":"Palmoplantar keratoderma"}]}},{"entity":"MGI:4361197","phenotype":{"types":[{"id":"MP:0010168","label":"increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number"}]}},{"entity":"_:genid1975962","phenotype":{"types":[{"id":"ZP:0001173","label":"abnormal(ly) decreased pigmentation whole organism"}]}},{"entity":"ClinVarVariant:208016","phenotype":{"types":[{"id":"HP:0002748","label":"Rickets"}]}},{"entity":"ClinVarVariant:53905","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:11586","phenotype":{"types":[{"id":"HP:0002860","label":"Squamous cell carcinoma"}]}},{"entity":"ClinVarVariant:30467","phenotype":{"types":[{"id":"HP:0002949","label":"Fused cervical vertebrae"}]}},{"entity":"ClinVarVariant:809","phenotype":{"types":[{"id":"HP:0000706","label":"Unerupted tooth"}]}},{"entity":"MGI:2183813","phenotype":{"types":[{"id":"MP:0000646","label":"enlarged adrenocortical cells"}]}},{"entity":"ClinVarVariant:64943","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"ClinVarVariant:3904","phenotype":{"types":[{"id":"HP:0003495","label":"GM2-ganglioside accumulation"}]}},{"entity":"MGI:3653699","phenotype":{"types":[{"id":"HP:0005048","label":"Synostosis of carpal bones"}]}},{"entity":"MGI:5559460","phenotype":{"types":[{"id":"MP:0001666","label":"abnormal intestinal absorption"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004498-WBRNAi00099563","phenotype":{"types":[{"id":"WBPhenotype:0000961","label":"pattern of transgene expression variant"}]}},{"entity":"ClinVarVariant:101394","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:10345","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:4933","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:49479","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"ClinVarVariant:212265","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:49115","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:15234","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00012221-WBRNAi00097504","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:209067","phenotype":{"types":[{"id":"HP:0002331","label":"Headache (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:1257","phenotype":{"types":[{"id":"HP:0000926","label":"Platyspondyly"}]}},{"entity":"ClinVarVariant:36379","phenotype":{"types":[{"id":"HP:0000684","label":"Delayed eruption of teeth"}]}},{"entity":"AQTL:15392","phenotype":{"types":[{"id":"AQTLTrait:1076","label":"Gestation length"}]}},{"entity":"ClinVarVariant:92880","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:694","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"ClinVarVariant:209043","phenotype":{"types":[{"id":"HP:0001115","label":"Posterior polar cataract"}]}},{"entity":"ClinVarVariant:35838","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"ClinVarVariant:216398","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:10122","phenotype":{"types":[{"id":"HP:0100310","label":"Epidural hemorrhage"}]}},{"entity":"ClinVarVariant:17784","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"FlyBase:FBal0033446","phenotype":{"types":[{"id":"FBbt:00000004PHENOTYPE","label":"Drosophila head phenotype"}]}},{"entity":"MGI:3526165","phenotype":{"types":[{"id":"GO:0032880PHENOTYPE","label":"regulation of protein localization phenotype"}]}},{"entity":"ClinVarVariant:210447","phenotype":{"types":[{"id":"HP:0005599","label":"Hypopigmentation of hair"}]}},{"entity":"ClinVarVariant:10285","phenotype":{"types":[{"id":"HP:0001369","label":"Arthritis"}]}},{"entity":"ClinVarVariant:126394","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"ClinVarVariant:9599","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:216023","phenotype":{"types":[{"id":"HP:0000035","label":"Abnormality of the testis"}]}},{"entity":"ClinVarVariant:10738","phenotype":{"types":[{"id":"HP:0000763","label":"Sensory neuropathy"}]}},{"entity":"ClinVarVariant:3571","phenotype":{"types":[{"id":"HP:0010044","label":"Short 4th metacarpal"}]}},{"entity":"ClinVarVariant:67881","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:8710","phenotype":{"types":[{"id":"HP:0002823","label":"Abnormality of the femur"}]}},{"entity":"ClinVarVariant:159228","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"ClinVarVariant:36081","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:161334","phenotype":{"types":[{"id":"HP:0005293","label":"Venous insufficiency"}]}},{"entity":"MGI:3762530","phenotype":{"types":[{"id":"MP:0002020","label":"increased tumor incidence"}]}},{"entity":"ClinVarVariant:188302","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:11342","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"ClinVarVariant:10751","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:53923","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"MGI:5320577","phenotype":{"types":[{"id":"MP:0006059","label":"decreased susceptibility to ischemic brain injury"}]}},{"entity":"ClinVarVariant:17332","phenotype":{"types":[{"id":"HP:0002659","label":"Increased susceptibility to fractures"}]}},{"entity":"ClinVarVariant:66101","phenotype":{"types":[{"id":"HP:0011109","label":"Chronic sinusitis"}]}},{"entity":"ClinVarVariant:11596","phenotype":{"types":[{"id":"HP:0002860","label":"Squamous cell carcinoma"}]}},{"entity":"ClinVarVariant:13848","phenotype":{"types":[{"id":"HP:0007542","label":"Absent pigmentation of the ventral chest"}]}},{"entity":"ClinVarVariant:209019","phenotype":{"types":[{"id":"HP:0000777","label":"Abnormality of the thymus"}]}},{"entity":"ClinVarVariant:166927","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"AQTL:4620","phenotype":{"types":[{"id":"AQTLTrait:1099","label":"Milking speed"}]}},{"entity":"ClinVarVariant:53677","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:159171","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"ClinVarVariant:17976","phenotype":{"types":[{"id":"HP:0006530","label":"Interstitial pulmonary disease"}]}},{"entity":"ClinVarVariant:39444","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:96580","phenotype":{"types":[{"id":"HP:0002179","label":"Opisthotonus"}]}},{"entity":"MGI:1856097","phenotype":{"types":[{"id":"MP:0010908","label":"dilated pulmonary alveolar ducts"}]}},{"entity":"ClinVarVariant:7314","phenotype":{"types":[{"id":"HP:0000678","label":"Dental crowding"}]}},{"entity":"ClinVarVariant:158904","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:215720","phenotype":{"types":[{"id":"HP:0100697","label":"Neurofibrosarcoma"}]}},{"entity":"MGI:2384515","phenotype":{"types":[{"id":"MP:0001405","label":"impaired coordination"}]}},{"entity":"MGI:3576024","phenotype":{"types":[{"id":"HP:0000157","label":"Abnormality of the tongue"}]}},{"entity":"ClinVarVariant:21535","phenotype":{"types":[{"id":"HP:0001256","label":"Intellectual disability, mild"}]}},{"entity":"ClinVarVariant:192298","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"ClinVarVariant:215688","phenotype":{"types":[{"id":"HP:0003468","label":"Abnormality of the vertebrae"}]}},{"entity":"dbSNP:rs110801629","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ZFIN:ZDB-ALT-980203-452","phenotype":{"types":[{"id":"ZP:0000148","label":"abnormal(ly) increased width notochord"}]}},{"entity":"ClinVarVariant:209053","phenotype":{"types":[{"id":"HP:0001648","label":"Cor pulmonale"}]}},{"entity":"ClinVarVariant:30527","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ZFIN:ZDB-ALT-020422-8","phenotype":{"types":[{"id":"ZP:0002275","label":"abnormal(ly) necrotic trunk"}]}},{"entity":"ClinVarVariant:10249","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:101204","phenotype":{"types":[{"id":"HP:0010318","label":"Aplasia/Hypoplasia of the abdominal wall musculature"}]}},{"entity":"ClinVarVariant:9956","phenotype":{"types":[{"id":"HP:0001923","label":"Reticulocytosis"}]}},{"entity":"ClinVarVariant:126447","phenotype":{"types":[{"id":"HP:0100689","label":"Decreased corneal thickness"}]}},{"entity":"ClinVarVariant:93336","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:36957","phenotype":{"types":[{"id":"HP:0001539","label":"Omphalocele"}]}},{"entity":"ClinVarVariant:190118","phenotype":{"types":[{"id":"HP:0002015","label":"Dysphagia"}]}},{"entity":"ClinVarVariant:210474","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:159234","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:40522","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:605","phenotype":{"types":[{"id":"HP:0004923","label":"Hyperphenylalaninemia"}]}},{"entity":"MGI:2155766","phenotype":{"types":[{"id":"MP:0002836","label":"abnormal chorion morphology"}]}},{"entity":"MGI:3511363","phenotype":{"types":[{"id":"HP:0001539","label":"Omphalocele"}]}},{"entity":"ClinVarVariant:41344","phenotype":{"types":[{"id":"HP:0007067","label":"Distal peripheral sensory neuropathy"}]}},{"entity":"ClinVarVariant:38578","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"MGI:4842477","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:82347","phenotype":{"types":[{"id":"HP:0006753","label":"Neoplasm of the stomach"}]}},{"entity":"MGI:1856222","phenotype":{"types":[{"id":"MP:0002938","label":"white spotting"}]}},{"entity":"ClinVarVariant:49718","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"MGI:2652711","phenotype":{"types":[{"id":"MP:0011750","label":"abnormal seminiferous tubule epithelium morphology"}]}},{"entity":"MGI:3056917","phenotype":{"types":[{"id":"MP:0001402","label":"hypoactivity"}]}},{"entity":"MGI:2158307","phenotype":{"types":[{"id":"MP:0002722","label":"abnormal immune system organ morphology"}]}},{"entity":"ClinVarVariant:40526","phenotype":{"types":[{"id":"HP:0000520","label":"Proptosis"}]}},{"entity":"ClinVarVariant:41247","phenotype":{"types":[{"id":"HP:0003429","label":"CNS hypomyelination"}]}},{"entity":"ClinVarVariant:53618","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"FlyBase:FBal0207560","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:216725","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:158962","phenotype":{"types":[{"id":"HP:0011308","label":"Slender toe"}]}},{"entity":"MGI:4880750","phenotype":{"types":[{"id":"MP:0008702","label":"increased interleukin-5 secretion"}]}},{"entity":"AQTL:23951","phenotype":{"types":[{"id":"AQTLTrait:1196","label":"Abomasum displacement"}]}},{"entity":"MGI:1929775","phenotype":{"types":[{"id":"MP:0008148","label":"abnormal rib-sternum attachment"}]}},{"entity":"ClinVarVariant:53716","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:36083","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:88836","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:35713","phenotype":{"types":[{"id":"HP:0000934","label":"Chondrocalcinosis"}]}},{"entity":"ClinVarVariant:190232","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"ClinVarVariant:190368","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:156281","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:210008","phenotype":{"types":[{"id":"HP:0002301","label":"Hemiplegia"}]}},{"entity":"ClinVarVariant:56669","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:8259","phenotype":{"types":[{"id":"HP:0001056","label":"Milia"}]}},{"entity":"ClinVarVariant:10619","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:135769","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:25004","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"MGI:1856699","phenotype":{"types":[{"id":"MP:0001212","label":"skin lesions"}]}},{"entity":"ClinVarVariant:10217","phenotype":{"types":[{"id":"HP:0011892","label":"Vitamin K deficiency"}]}},{"entity":"ClinVarVariant:60779","phenotype":{"types":[{"id":"HP:0008180","label":"Mildly elevated creatine phosphokinase"}]}},{"entity":"ClinVarVariant:53779","phenotype":{"types":[{"id":"HP:0100660","label":"Dyskinesia"}]}},{"entity":"ClinVarVariant:24687","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:100728","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ClinVarVariant:156381","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:41692","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"FlyBase:FBal0126487","phenotype":{"types":[{"id":"FBbt:00001682PHENOTYPE","label":"Drosophila embryonic/larval hemocoel phenotype"}]}},{"entity":"ClinVarVariant:52398","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006700-WBRNAi00061477","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"ClinVarVariant:183367","phenotype":{"types":[{"id":"HP:0005218","label":"Anoperineal fistula"}]}},{"entity":"ClinVarVariant:2482","phenotype":{"types":[{"id":"HP:0001608","label":"Abnormality of the voice"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001892-WBRNAi00025035","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:42345","phenotype":{"types":[{"id":"HP:0004933","label":"Ascending aortic dissection"}]}},{"entity":"ClinVarVariant:9983","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:21565","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:5633","phenotype":{"types":[{"id":"HP:0000141","label":"Amenorrhea"}]}},{"entity":"ClinVarVariant:16624","phenotype":{"types":[{"id":"HP:0003762","label":"Uterus didelphys"}]}},{"entity":"ClinVarVariant:181715","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:199203","phenotype":{"types":[{"id":"HP:0002486","label":"Myotonia"}]}},{"entity":"ClinVarVariant:53715","phenotype":{"types":[{"id":"HP:0004936","label":"Venous thrombosis"}]}},{"entity":"ClinVarVariant:209059","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:56253","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:14091","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:12493","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"MGI:5468098","phenotype":{"types":[{"id":"HP:0011849","label":"Abnormal bone ossification"}]}},{"entity":"MGI:5443922","phenotype":{"types":[{"id":"HP:0003233","label":"Hypoalphalipoproteinemia"}]}},{"entity":"ClinVarVariant:207574","phenotype":{"types":[{"id":"HP:0002495","label":"Impaired vibratory sensation"}]}},{"entity":"WormBase:WBVar00242117","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:53226","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:11430","phenotype":{"types":[{"id":"HP:0008839","label":"Hypoplastic pelvis"}]}},{"entity":"ClinVarVariant:10058","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"ClinVarVariant:158385","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"MGI:5141269","phenotype":{"types":[{"id":"HP:0002591","label":"Polyphagia"}]}},{"entity":"ClinVarVariant:181494","phenotype":{"types":[{"id":"HP:0010541","label":"Cutis gyrata of scalp"}]}},{"entity":"ClinVarVariant:12391","phenotype":{"types":[{"id":"HP:0011364","label":"White hair"}]}},{"entity":"ClinVarVariant:53911","phenotype":{"types":[{"id":"HP:0003453","label":"Antineutrophil antibody positivity"}]}},{"entity":"MGI:2151589","phenotype":{"types":[{"id":"MP:0009355","label":"increased liver triglyceride level"}]}},{"entity":"ClinVarVariant:38415","phenotype":{"types":[{"id":"HP:0003264","label":"Deficiency of N-acetylglucosamine-1-phosphotransferase"}]}},{"entity":"ClinVarVariant:30832","phenotype":{"types":[{"id":"HP:0100790","label":"Hernia"}]}},{"entity":"FlyBase:FBal0209815","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:180622","phenotype":{"types":[{"id":"HP:0004430","label":"Severe combined immunodeficiency"}]}},{"entity":"ClinVarVariant:24371","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"ClinVarVariant:156327","phenotype":{"types":[{"id":"HP:0100512","label":"Vitamin D deficiency"}]}},{"entity":"ClinVarVariant:54054","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:197080","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"MGI:4358721","phenotype":{"types":[{"id":"MP:0001523","label":"impaired righting response"}]}},{"entity":"ClinVarVariant:199965","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"ClinVarVariant:29","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"MGI:3623117","phenotype":{"types":[{"id":"MP:0004918","label":"abnormal negative T cell selection"}]}},{"entity":"ClinVarVariant:158914","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:30626","phenotype":{"types":[{"id":"HP:0100532","label":"Scleritis"}]}},{"entity":"ClinVarVariant:53187","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"FlyBase:FBal0043110","phenotype":{"types":[{"id":"FBbt:00000169PHENOTYPE","label":"embryonic mesothoracic segment phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017282-WBRNAi00102984","phenotype":{"types":[{"id":"WBPhenotype:0000462","label":"paraquat hypersensitive"}]}},{"entity":"ClinVarVariant:53320","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"MGI:3639295","phenotype":{"types":[{"id":"HP:0011121","label":"Abnormality of skin morphology"}]}},{"entity":"ClinVarVariant:215752","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"ClinVarVariant:215780","phenotype":{"types":[{"id":"HP:0003241","label":"External genital hypoplasia"}]}},{"entity":"ClinVarVariant:91650","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:55948","phenotype":{"types":[{"id":"HP:0006887","label":"Intellectual disability, progressive"}]}},{"entity":"ClinVarVariant:17209","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"ClinVarVariant:1461","phenotype":{"types":[{"id":"HP:0006597","label":"Diaphragmatic paralysis"}]}},{"entity":"ClinVarVariant:4310","phenotype":{"types":[{"id":"HP:0003540","label":"Impaired platelet aggregation"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00194986-WBRNAi00085581","phenotype":{"types":[{"id":"WBPhenotype:0001951","label":"pachytene region organization variant"}]}},{"entity":"ClinVarVariant:5069","phenotype":{"types":[{"id":"HP:0100716","label":"Self-injurious behavior"}]}},{"entity":"ClinVarVariant:11644","phenotype":{"types":[{"id":"HP:0000395","label":"Prominent antihelix"}]}},{"entity":"ClinVarVariant:210461","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:217066","phenotype":{"types":[{"id":"HP:0009736","label":"Tibial pseudoarthrosis"}]}},{"entity":"ClinVarVariant:41306","phenotype":{"types":[{"id":"HP:0011449","label":"Knee clonus"}]}},{"entity":"ClinVarVariant:216230","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:16085","phenotype":{"types":[{"id":"HP:0007495","label":"Prematurely aged appearance"}]}},{"entity":"MGI:3785252","phenotype":{"types":[{"id":"MP:0008874","label":"decreased physiological sensitivity to xenobiotic"}]}},{"entity":"_:genid1975900","phenotype":{"types":[{"id":"ZP:0000038","label":"abnormal(ly) edematous pericardium"}]}},{"entity":"ClinVarVariant:11540","phenotype":{"types":[{"id":"HP:0002007","label":"Frontal bossing"}]}},{"entity":"MGI:3624263","phenotype":{"types":[{"id":"MP:0011186","label":"abnormal visceral endoderm morphology"}]}},{"entity":"ClinVarVariant:53939","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ClinVarVariant:156552","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"ClinVarVariant:24978","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:41131","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:36033","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"FlyBase:FBal0210612","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:2149","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ClinVarVariant:24396","phenotype":{"types":[{"id":"HP:0008063","label":"Aplasia/Hypoplasia of the lens"}]}},{"entity":"ClinVarVariant:24651","phenotype":{"types":[{"id":"HP:0011501","label":"Anterior lenticonus"}]}},{"entity":"ClinVarVariant:24375","phenotype":{"types":[{"id":"HP:0000093","label":"Proteinuria"}]}},{"entity":"ClinVarVariant:25310","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:40502","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"ClinVarVariant:167188","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:2128","phenotype":{"types":[{"id":"HP:0000612","label":"Iris coloboma"}]}},{"entity":"MGI:2385717","phenotype":{"types":[{"id":"MP:0002961","label":"abnormal axon guidance"}]}},{"entity":"MGI:2683050","phenotype":{"types":[{"id":"HP:0004324","label":"Increased body weight"}]}},{"entity":"ClinVarVariant:50055","phenotype":{"types":[{"id":"HP:0009716","label":"Subependymal nodules"}]}},{"entity":"ClinVarVariant:7853","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"ClinVarVariant:142534","phenotype":{"types":[{"id":"HP:0001562","label":"Oligohydramnios"}]}},{"entity":"MGI:5470094","phenotype":{"types":[{"id":"HP:0002450","label":"Abnormal motor neuron morphology"}]}},{"entity":"MGI:5441311","phenotype":{"types":[{"id":"MP:0009763","label":"increased sensitivity to induced morbidity/mortality"}]}},{"entity":"MGI:5007063","phenotype":{"types":[{"id":"MP:0002116","label":"abnormal craniofacial bone morphology"}]}},{"entity":"ClinVarVariant:188088","phenotype":{"types":[{"id":"HP:0002669","label":"Osteosarcoma"}]}},{"entity":"ClinVarVariant:196277","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:38289","phenotype":{"types":[{"id":"HP:0002789","label":"Tachypnea"}]}},{"entity":"ClinVarVariant:16741","phenotype":{"types":[{"id":"HP:0000153","label":"Abnormality of the mouth"}]}},{"entity":"ClinVarVariant:10654","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"ClinVarVariant:5508","phenotype":{"types":[{"id":"HP:0000882","label":"Hypoplastic scapulae"}]}},{"entity":"ClinVarVariant:211503","phenotype":{"types":[{"id":"HP:0001195","label":"Single umbilical artery"}]}},{"entity":"ClinVarVariant:53915","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:3756","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:42443","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"MGI:3798768","phenotype":{"types":[{"id":"MP:0005076","label":"abnormal cell differentiation"}]}},{"entity":"ClinVarVariant:101503","phenotype":{"types":[{"id":"HP:0010752","label":"Cleft mandible"}]}},{"entity":"ClinVarVariant:64997","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:1539","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:101108","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"ClinVarVariant:43202","phenotype":{"types":[{"id":"HP:0000360","label":"Tinnitus"}]}},{"entity":"ClinVarVariant:5943","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:24508","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:38311","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:1128","phenotype":{"types":[{"id":"HP:0000895","label":"Lateral clavicle hook"}]}},{"entity":"MGI:2388126","phenotype":{"types":[{"id":"MP:0002113","label":"abnormal skeleton development"}]}},{"entity":"ClinVarVariant:96576","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"ClinVarVariant:53236","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:193747","phenotype":{"types":[{"id":"HP:0001256","label":"Intellectual disability, mild"}]}},{"entity":"ClinVarVariant:126412","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:94109","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"dbSNP:rs41666553","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:31217","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:54003","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:25350","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"ClinVarVariant:198365","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"ClinVarVariant:24676","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"ClinVarVariant:94210","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:101296","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"DOID:11726","phenotype":{"types":[{"id":"HP:0001638","label":"Cardiomyopathy"}]}},{"entity":"FlyBase:FBal0118076","phenotype":{"types":[{"id":"FBcv:0000394","label":"circadian rhythm defective"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00009186-WBRNAi00045737","phenotype":{"types":[{"id":"WBPhenotype:0000640","label":"egg laying variant"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003186-WBRNAi00085575","phenotype":{"types":[{"id":"WBPhenotype:0000291","label":"no oocytes"}]}},{"entity":"ClinVarVariant:24755","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:11836","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:158924","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:67977","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:55823","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050523-1-ZDB-MRPHLNO-080703-4","phenotype":{"types":[{"id":"ZP:0007823","label":"abnormal(ly) increased width floor plate rhombomere region"}]}},{"entity":"ClinVarVariant:65018","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:67936","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:188997","phenotype":{"types":[{"id":"HP:0001954","label":"Episodic fever"}]}},{"entity":"ClinVarVariant:190776","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:50061","phenotype":{"types":[{"id":"HP:0000269","label":"Prominent occiput"}]}},{"entity":"ClinVarVariant:13674","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-030131-180-ZDB-MRPHLNO-110715-2","phenotype":{"types":[{"id":"GO:0035188PHENOTYPE","label":"hatching phenotype"}]}},{"entity":"ClinVarVariant:6639","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"FlyBase:FBal0205870","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:54073","phenotype":{"types":[{"id":"HP:0000966","label":"Hypohidrosis"}]}},{"entity":"MGI:3588578","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:50112","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"ClinVarVariant:11860","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008688-WBRNAi00080126","phenotype":{"types":[{"id":"ZP:0000676","label":"abnormal(ly) increased rate cell proliferation"}]}},{"entity":"ClinVarVariant:18086","phenotype":{"types":[{"id":"HP:0002884","label":"Hepatoblastoma"}]}},{"entity":"ClinVarVariant:7516","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"ClinVarVariant:94475","phenotype":{"types":[{"id":"HP:0002948","label":"Vertebral fusion"}]}},{"entity":"dbSNP:rs12793173","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:1532","phenotype":{"types":[{"id":"HP:0010980","label":"Hyperlipoproteinemia"}]}},{"entity":"ClinVarVariant:158567","phenotype":{"types":[{"id":"HP:0009836","label":"Broad distal phalanx of finger"}]}},{"entity":"ClinVarVariant:188263","phenotype":{"types":[{"id":"HP:0002321","label":"Vertigo"}]}},{"entity":"ClinVarVariant:141451","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00015583-WBRNAi00077058","phenotype":{"types":[{"id":"WBPhenotype:0000012","label":"dauer constitutive"}]}},{"entity":"ClinVarVariant:208075","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"MGI:2156546","phenotype":{"types":[{"id":"MP:0005597","label":"decreased susceptibility to type I hypersensitivity reaction"}]}},{"entity":"MGI:5285080","phenotype":{"types":[{"id":"MP:0013209","label":"abnormal motile cilium physiology"}]}},{"entity":"ClinVarVariant:38281","phenotype":{"types":[{"id":"HP:0011131","label":"Perianal rash"}]}},{"entity":"ClinVarVariant:53127","phenotype":{"types":[{"id":"HP:0006696","label":"Polymorphic and polytopic ventricular extrasystoles"}]}},{"entity":"MGI:3822156","phenotype":{"types":[{"id":"MP:0000281","label":"abnormal interventricular septum morphology"}]}},{"entity":"ClinVarVariant:49660","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:39711","phenotype":{"types":[{"id":"HP:0001171","label":"Split hand"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003947-WBRNAi00085486","phenotype":{"types":[{"id":"WBPhenotype:0001950","label":"diplotene region organization variant"}]}},{"entity":"ClinVarVariant:127405","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:43995","phenotype":{"types":[{"id":"HP:0001678","label":"Atrioventricular block"}]}},{"entity":"ClinVarVariant:188886","phenotype":{"types":[{"id":"HP:0001878","label":"Hemolytic anemia"}]}},{"entity":"ClinVarVariant:101248","phenotype":{"types":[{"id":"HP:0100627","label":"Displacement of the external urethral meatus"}]}},{"entity":"ClinVarVariant:17360","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006375-WBRNAi00097656","phenotype":{"types":[{"id":"ZP:0004962","label":"abnormal(ly) increased rate apoptotic process"}]}},{"entity":"ClinVarVariant:38942","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:8482","phenotype":{"types":[{"id":"HP:0001332","label":"Dystonia"}]}},{"entity":"ClinVarVariant:12497","phenotype":{"types":[{"id":"HP:0011039","label":"Abnormality of the helix"}]}},{"entity":"ClinVarVariant:1480","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:189710","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:690","phenotype":{"types":[{"id":"HP:0000914","label":"Shield chest"}]}},{"entity":"ClinVarVariant:136123","phenotype":{"types":[{"id":"HP:0000980","label":"Pallor"}]}},{"entity":"MGI:3040471","phenotype":{"types":[{"id":"HP:0011111","label":"Abnormality of immune serum protein physiology"}]}},{"entity":"ClinVarVariant:210716","phenotype":{"types":[{"id":"HP:0001231","label":"Abnormality of the fingernails"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001967-WBRNAi00070035","phenotype":{"types":[{"id":"WBPhenotype:0000696","label":"everted vulva"}]}},{"entity":"ClinVarVariant:53210","phenotype":{"types":[{"id":"HP:0006536","label":"Obstructive lung disease"}]}},{"entity":"ClinVarVariant:53246","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:24716","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:212636","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:10118","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"ClinVarVariant:17484","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:202177","phenotype":{"types":[{"id":"HP:0010780","label":"Hyperacusis"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050419-261-ZDB-MRPHLNO-130117-3","phenotype":{"types":[{"id":"ZP:0002516","label":"abnormal(ly) cystic pronephric glomerulus"}]}},{"entity":"ClinVarVariant:66036","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"dbSNP:rs586716","phenotype":{"types":[{"id":"HP:0003418","label":"Back pain"}]}},{"entity":"ClinVarVariant:101414","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:49414","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"ClinVarVariant:166862","phenotype":{"types":[{"id":"HP:0000689","label":"Dental malocclusion"}]}},{"entity":"ClinVarVariant:41344","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"MGI:5431878","phenotype":{"types":[{"id":"HP:0012373","label":"Abnormal eye physiology"}]}},{"entity":"ClinVarVariant:155889","phenotype":{"types":[{"id":"HP:0001950","label":"Respiratory alkalosis"}]}},{"entity":"ClinVarVariant:1743","phenotype":{"types":[{"id":"HP:0200118","label":"Malabsorption of Vitamin B12"}]}},{"entity":"ClinVarVariant:65028","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:24275","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"ClinVarVariant:53680","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:92800","phenotype":{"types":[{"id":"HP:0000219","label":"Thin upper lip vermilion"}]}},{"entity":"ClinVarVariant:13997","phenotype":{"types":[{"id":"HP:0004429","label":"Recurrent viral infections"}]}},{"entity":"ClinVarVariant:54064","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"MGI:1857348","phenotype":{"types":[{"id":"HP:0100495","label":"Mastocytosis"}]}},{"entity":"ClinVarVariant:40512","phenotype":{"types":[{"id":"HP:0000276","label":"Long face"}]}},{"entity":"FlyBase:FBal0095694","phenotype":{"types":[{"id":"FBbt:00004200PHENOTYPE","label":"retina phenotype"}]}},{"entity":"MGI:2677682","phenotype":{"types":[{"id":"MP:0002813","label":"microcytosis"}]}},{"entity":"dbSNP:rs7045640","phenotype":{"types":[{"id":"HP:0001489","label":"Posterior vitreous detachment"}]}},{"entity":"ClinVarVariant:5094","phenotype":{"types":[{"id":"HP:0002757","label":"Recurrent fractures"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002064-WBRNAi00063098","phenotype":{"types":[{"id":"WBPhenotype:0000291","label":"no oocytes"}]}},{"entity":"ClinVarVariant:11134","phenotype":{"types":[{"id":"HP:0001891","label":"Iron deficiency anemia"}]}},{"entity":"ClinVarVariant:189284","phenotype":{"types":[{"id":"HP:0008572","label":"External ear malformation"}]}},{"entity":"MGI:3057163","phenotype":{"types":[{"id":"HP:0001882","label":"Leukopenia"}]}},{"entity":"MGI:3846101","phenotype":{"types":[{"id":"MP:0002874","label":"decreased hemoglobin content"}]}},{"entity":"ClinVarVariant:12051","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:56263","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"AQTL:11570","phenotype":{"types":[{"id":"AQTLTrait:224","label":"Small intestinal Escherichia coli F18 receptor"}]}},{"entity":"ClinVarVariant:40551","phenotype":{"types":[{"id":"HP:0010541","label":"Cutis gyrata of scalp"}]}},{"entity":"ClinVarVariant:54031","phenotype":{"types":[{"id":"HP:0005948","label":"Cystic lung disease"}]}},{"entity":"ClinVarVariant:42343","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"MGI:3512077","phenotype":{"types":[{"id":"MP:0000750","label":"abnormal muscle regeneration"}]}},{"entity":"ClinVarVariant:50982","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"MGI:2448247","phenotype":{"types":[{"id":"MP:0001176","label":"abnormal lung development"}]}},{"entity":"ClinVarVariant:53871","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004078-WBRNAi00091973","phenotype":{"types":[{"id":"ZP:0000305","label":"abnormal(ly) arrested embryo development"}]}},{"entity":"FlyBase:FBal0200222","phenotype":{"types":[{"id":"FBbt:00005149PHENOTYPE","label":"ganglion mother cell phenotype"}]}},{"entity":"ClinVarVariant:216429","phenotype":{"types":[{"id":"HP:0100280","label":"Crohn's disease"}]}},{"entity":"ClinVarVariant:2392","phenotype":{"types":[{"id":"HP:0003218","label":"Oroticaciduria"}]}},{"entity":"ClinVarVariant:142966","phenotype":{"types":[{"id":"HP:0000777","label":"Abnormality of the thymus"}]}},{"entity":"MGI:3624543","phenotype":{"types":[{"id":"MP:0000951","label":"sporadic seizures"}]}},{"entity":"ClinVarVariant:133608","phenotype":{"types":[{"id":"HP:0002344","label":"Progressive neurologic deterioration"}]}},{"entity":"ClinVarVariant:211626","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:9656","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:25215","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:10572","phenotype":{"types":[{"id":"HP:0005186","label":"Synovial hypertrophy"}]}},{"entity":"MGI:3722688","phenotype":{"types":[{"id":"HP:0003022","label":"Hypoplasia of the ulna"}]}},{"entity":"ClinVarVariant:93129","phenotype":{"types":[{"id":"HP:0002371","label":"Loss of speech"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004806-WBRNAi00036044","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"MGI:2386742","phenotype":{"types":[{"id":"HP:0001719","label":"Double outlet right ventricle"}]}},{"entity":"ClinVarVariant:12534","phenotype":{"types":[{"id":"HP:0002659","label":"Increased susceptibility to fractures"}]}},{"entity":"ClinVarVariant:53491","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"WormBase:WBVar00087758","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:100772","phenotype":{"types":[{"id":"HP:0000174","label":"Abnormality of the palate"}]}},{"entity":"FlyBase:FBal0269186","phenotype":{"types":[{"id":"FBbt:00004646PHENOTYPE","label":"tarsal segment phenotype"}]}},{"entity":"ClinVarVariant:209167","phenotype":{"types":[{"id":"HP:0000666","label":"Horizontal nystagmus"}]}},{"entity":"AQTL:29399","phenotype":{"types":[{"id":"AQTLTrait:1085","label":"Degree of Spotting"}]}},{"entity":"ZFIN:ZDB-ALT-090611-2","phenotype":{"types":[{"id":"GO:0045765PHENOTYPE","label":"regulation of angiogenesis phenotype"}]}},{"entity":"ClinVarVariant:36053","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:101388","phenotype":{"types":[{"id":"HP:0009906","label":"Aplasia/Hypoplasia of the earlobes"}]}},{"entity":"MGI:3605473","phenotype":{"types":[{"id":"MP:0004167","label":"abnormal cingulate gyrus morphology"}]}},{"entity":"MGI:4433578","phenotype":{"types":[{"id":"MP:0004527","label":"abnormal outer hair cell stereociliary bundle morphology"}]}},{"entity":"ClinVarVariant:2324","phenotype":{"types":[{"id":"HP:0001315","label":"Reduced tendon reflexes"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-061103-265-ZDB-MRPHLNO-140606-7","phenotype":{"types":[{"id":"ZP:0004552","label":"abnormal(ly) bilateral symmetry heart tube"}]}},{"entity":"ClinVarVariant:181833","phenotype":{"types":[{"id":"HP:0100777","label":"Exostoses"}]}},{"entity":"ClinVarVariant:93455","phenotype":{"types":[{"id":"HP:0000939","label":"Osteoporosis"}]}},{"entity":"MGI:3817754","phenotype":{"types":[{"id":"HP:0000859","label":"Hyperaldosteronism"}]}},{"entity":"ClinVarVariant:211657","phenotype":{"types":[{"id":"HP:0000776","label":"Congenital diaphragmatic hernia"}]}},{"entity":"ClinVarVariant:35972","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:4674","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"ClinVarVariant:8953","phenotype":{"types":[{"id":"HP:0006380","label":"Knee flexion contracture"}]}},{"entity":"FlyBase:FBal0221490","phenotype":{"types":[{"id":"FBbt:00004483PHENOTYPE","label":"Drosophila ptilinum phenotype"}]}},{"entity":"FlyBase:FBal0050220","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"FlyBase:FBal0200679","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"MGI:2178387","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:41120","phenotype":{"types":[{"id":"HP:0100612","label":"Odontogenic neoplasm"}]}},{"entity":"ClinVarVariant:13723","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:161333","phenotype":{"types":[{"id":"HP:0001038","label":"Warfarin-induced skin necrosis"}]}},{"entity":"ClinVarVariant:6099","phenotype":{"types":[{"id":"HP:0003312","label":"Abnormal form of the vertebral bodies"}]}},{"entity":"ClinVarVariant:41180","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:9430","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:99932","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:36072","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:1987","phenotype":{"types":[{"id":"HP:0000057","label":"obsolete Clitoromegaly"}]}},{"entity":"ClinVarVariant:158899","phenotype":{"types":[{"id":"HP:0003324","label":"Generalized muscle weakness"}]}},{"entity":"ZFIN:ZDB-ALT-041008-4","phenotype":{"types":[{"id":"ZP:0000407","label":"abnormal(ly) decreased width head"}]}},{"entity":"ClinVarVariant:7292","phenotype":{"types":[{"id":"HP:0001053","label":"Hypopigmented skin patches"}]}},{"entity":"ClinVarVariant:67378","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:36284","phenotype":{"types":[{"id":"HP:0000832","label":"Primary hypothyroidism"}]}},{"entity":"ClinVarVariant:194096","phenotype":{"types":[{"id":"HP:0000572","label":"Visual loss"}]}},{"entity":"ClinVarVariant:197503","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"AQTL:15249","phenotype":{"types":[{"id":"AQTLTrait:1027","label":"Marbling score"}]}},{"entity":"ClinVarVariant:49120","phenotype":{"types":[{"id":"HP:0008696","label":"Renal hamartoma"}]}},{"entity":"ClinVarVariant:12335","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:7979","phenotype":{"types":[{"id":"HP:0000400","label":"Macrotia"}]}},{"entity":"ClinVarVariant:49153","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:53913","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:133623","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ZFIN:ZDB-ALT-100723-4","phenotype":{"types":[{"id":"ZP:0007051","label":"abnormal(ly) dilated melanocyte"}]}},{"entity":"ClinVarVariant:88731","phenotype":{"types":[{"id":"HP:0012557","label":"EEG with centrotemporal focal spike waves"}]}},{"entity":"ClinVarVariant:49298","phenotype":{"types":[{"id":"HP:0009727","label":"Achromatic retinal patches"}]}},{"entity":"dbSNP:rs136851063","phenotype":{"types":[{"id":"AQTLTrait:1327","label":"Milk odd-chain fatty acid percentage"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00012059-WBRNAi00009225","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:30201","phenotype":{"types":[{"id":"HP:0000453","label":"Choanal atresia"}]}},{"entity":"MGI:2665856","phenotype":{"types":[{"id":"MP:0008190","label":"decreased transitional stage B cell number"}]}},{"entity":"ClinVarVariant:7165","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"ClinVarVariant:4078","phenotype":{"types":[{"id":"HP:0000529","label":"Progressive visual loss"}]}},{"entity":"ClinVarVariant:204238","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:53925","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"MGI:1860953","phenotype":{"types":[{"id":"MP:0008470","label":"abnormal spleen B cell follicle morphology"}]}},{"entity":"ClinVarVariant:53256","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"MGI:2386947","phenotype":{"types":[{"id":"HP:0010831","label":"Impaired proprioception"}]}},{"entity":"ClinVarVariant:158721","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:39468","phenotype":{"types":[{"id":"HP:0001845","label":"Overlapping toe"}]}},{"entity":"ClinVarVariant:53178","phenotype":{"types":[{"id":"HP:0004395","label":"Malnutrition"}]}},{"entity":"ClinVarVariant:158944","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00020820-WBRNAi00064595","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:53499","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:53943","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:209145","phenotype":{"types":[{"id":"HP:0006101","label":"Finger syndactyly"}]}},{"entity":"WormBase:WBVar00275350","phenotype":{"types":[{"id":"WBPhenotype:0000135","label":"gene expression level high"}]}},{"entity":"ClinVarVariant:53620","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:136034","phenotype":{"types":[{"id":"HP:0001587","label":"Primary ovarian failure"}]}},{"entity":"ClinVarVariant:10164","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:211738","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"ClinVarVariant:10083","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:211636","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:8570","phenotype":{"types":[{"id":"HP:0011423","label":"Hyperchloremia"}]}},{"entity":"ClinVarVariant:46449","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:93762","phenotype":{"types":[{"id":"HP:0000668","label":"Hypodontia"}]}},{"entity":"FlyBase:FBal0210265","phenotype":{"types":[{"id":"FBbt:00005169PHENOTYPE","label":"Drosophila trichogen cell phenotype"}]}},{"entity":"ClinVarVariant:38990","phenotype":{"types":[{"id":"HP:0003458","label":"EMG: myopathic abnormalities"}]}},{"entity":"ClinVarVariant:216803","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:3602","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:5712","phenotype":{"types":[{"id":"HP:0001611","label":"Nasal speech"}]}},{"entity":"MGI:4459725","phenotype":{"types":[{"id":"MP:0002044","label":"increased colonic adenoma incidence"}]}},{"entity":"ClinVarVariant:41109","phenotype":{"types":[{"id":"HP:0010297","label":"Bifid tongue"}]}},{"entity":"ClinVarVariant:101374","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"MGI:1857312","phenotype":{"types":[{"id":"MP:0001666","label":"abnormal intestinal absorption"}]}},{"entity":"dbSNP:rs4149584","phenotype":{"types":[{"id":"HP:0002321","label":"Vertigo"}]}},{"entity":"ClinVarVariant:5746","phenotype":{"types":[{"id":"HP:0001622","label":"Premature birth"}]}},{"entity":"ClinVarVariant:53799","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"ClinVarVariant:50176","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:155800","phenotype":{"types":[{"id":"HP:0011034","label":"Amyloidosis"}]}},{"entity":"ClinVarVariant:36063","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:100773","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"ClinVarVariant:6866","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"MGI:3527932","phenotype":{"types":[{"id":"MP:0002705","label":"dilated renal tubules"}]}},{"entity":"ClinVarVariant:9137","phenotype":{"types":[{"id":"HP:0003124","label":"Hypercholesterolemia"}]}},{"entity":"ClinVarVariant:181716","phenotype":{"types":[{"id":"HP:0100542","label":"Abnormal localization of kidney"}]}},{"entity":"ClinVarVariant:189941","phenotype":{"types":[{"id":"HP:0005484","label":"Postnatal microcephaly"}]}},{"entity":"ClinVarVariant:132825","phenotype":{"types":[{"id":"HP:0001660","label":"Truncus arteriosus"}]}},{"entity":"ClinVarVariant:133530","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:14519","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:13072","phenotype":{"types":[{"id":"HP:0009824","label":"Upper limb undergrowth"}]}},{"entity":"ClinVarVariant:156361","phenotype":{"types":[{"id":"HP:0000062","label":"Ambiguous genitalia"}]}},{"entity":"ClinVarVariant:13783","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:7623","phenotype":{"types":[{"id":"HP:0000772","label":"Abnormality of the ribs"}]}},{"entity":"MGI:3821974","phenotype":{"types":[{"id":"MP:0001463","label":"abnormal spatial learning"}]}},{"entity":"ClinVarVariant:120296","phenotype":{"types":[{"id":"HP:0001010","label":"Hypopigmentation of the skin"}]}},{"entity":"ClinVarVariant:127306","phenotype":{"types":[{"id":"HP:0008256","label":"Adrenocortical adenoma"}]}},{"entity":"ClinVarVariant:12873","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:49281","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:211620","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"MGI:2384535","phenotype":{"types":[{"id":"MP:0001442","label":"decreased grooming behavior"}]}},{"entity":"ClinVarVariant:31180","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"ClinVarVariant:17088","phenotype":{"types":[{"id":"HP:0100279","label":"Ulcerative colitis"}]}},{"entity":"MGI:2653910","phenotype":{"types":[{"id":"MP:0008501","label":"increased IgG2b level"}]}},{"entity":"ClinVarVariant:1545","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:53266","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:50949","phenotype":{"types":[{"id":"HP:0000817","label":"Poor eye contact"}]}},{"entity":"FlyBase:FBal0156488","phenotype":{"types":[{"id":"GO:0042600PHENOTYPE","label":"chorion phenotype"}]}},{"entity":"ClinVarVariant:41058","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:101132","phenotype":{"types":[{"id":"HP:0000490","label":"Deeply set eye"}]}},{"entity":"ClinVarVariant:127247","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:53389","phenotype":{"types":[{"id":"HP:0000855","label":"Insulin resistance"}]}},{"entity":"ClinVarVariant:143808","phenotype":{"types":[{"id":"HP:0002376","label":"Developmental regression"}]}},{"entity":"ClinVarVariant:53545","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"ClinVarVariant:65904","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"_:genid1972746","phenotype":{"types":[{"id":"ZP:0001671","label":"abnormal(ly) disrupted locomotory behavior"}]}},{"entity":"ClinVarVariant:6040","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"MGI:5527336","phenotype":{"types":[{"id":"MP:0010639","label":"altered tumor pathology"}]}},{"entity":"ClinVarVariant:102556","phenotype":{"types":[{"id":"HP:0000709","label":"Psychosis"}]}},{"entity":"FlyBase:FBal0205295","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:21350","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"ClinVarVariant:54074","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"MGI:1861186","phenotype":{"types":[{"id":"MP:0004473","label":"absent nasal bone"}]}},{"entity":"ClinVarVariant:52388","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:42069","phenotype":{"types":[{"id":"HP:0002720","label":"IgA deficiency"}]}},{"entity":"ClinVarVariant:68059","phenotype":{"types":[{"id":"HP:0011704","label":"Sick sinus syndrome"}]}},{"entity":"MGI:2153356","phenotype":{"types":[{"id":"HP:0003687","label":"Centrally nucleated skeletal muscle fibers"}]}},{"entity":"ClinVarVariant:15624","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:197669","phenotype":{"types":[{"id":"HP:0010783","label":"Erythema"}]}},{"entity":"ClinVarVariant:7256","phenotype":{"types":[{"id":"HP:0002619","label":"Varicose veins"}]}},{"entity":"ClinVarVariant:36838","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:21094","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:53431","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"AQTL:24319","phenotype":{"types":[{"id":"AQTLTrait:1090","label":"Longissimus muscle area"}]}},{"entity":"ClinVarVariant:215458","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"ClinVarVariant:158744","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"ClinVarVariant:39713","phenotype":{"types":[{"id":"HP:0000194","label":"Open mouth"}]}},{"entity":"ClinVarVariant:36073","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:165770","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:4321","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:4179","phenotype":{"types":[{"id":"HP:0001332","label":"Dystonia"}]}},{"entity":"MGI:4435548","phenotype":{"types":[{"id":"MP:0002418","label":"increased susceptibility to viral infection"}]}},{"entity":"ClinVarVariant:50071","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:40493","phenotype":{"types":[{"id":"HP:0000824","label":"Growth hormone deficiency"}]}},{"entity":"ClinVarVariant:9192","phenotype":{"types":[{"id":"HP:0012307","label":"Spatulate ribs"}]}},{"entity":"ClinVarVariant:49601","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:31911","phenotype":{"types":[{"id":"HP:0000384","label":"Preauricular skin tag"}]}},{"entity":"ClinVarVariant:9767","phenotype":{"types":[{"id":"HP:0003236","label":"Elevated serum creatine phosphokinase"}]}},{"entity":"ClinVarVariant:66505","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:1578","phenotype":{"types":[{"id":"HP:0002487","label":"Hyperkinesis"}]}},{"entity":"ClinVarVariant:10048","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004397-WBRNAi00089816","phenotype":{"types":[{"id":"WBPhenotype:0000583","label":"dumpy"}]}},{"entity":"ClinVarVariant:10166","phenotype":{"types":[{"id":"HP:0005268","label":"Spontaneous abortion"}]}},{"entity":"ClinVarVariant:8653","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:17939","phenotype":{"types":[{"id":"HP:0010517","label":"Ectopic thymus tissue"}]}},{"entity":"MGI:1856276","phenotype":{"types":[{"id":"MP:0000914","label":"exencephaly"}]}},{"entity":"ClinVarVariant:1740","phenotype":{"types":[{"id":"HP:0001511","label":"Intrauterine growth retardation"}]}},{"entity":"ClinVarVariant:93124","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:53310","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:91640","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"NCBIGene:100126595","phenotype":{"types":[{"id":"HP:0100771","label":"Hypoperistalsis"}]}},{"entity":"ClinVarVariant:11715","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"MGI:2447334","phenotype":{"types":[{"id":"HP:0012757","label":"Abnormal neuron morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008149-WBRNAi00008529","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:49227","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:143544","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"dbSNP:rs81339346","phenotype":{"types":[{"id":"AQTLTrait:1483","label":"Red blood cell count"}]}},{"entity":"ClinVarVariant:127155","phenotype":{"types":[{"id":"HP:0000622","label":"Blurred vision"}]}},{"entity":"ClinVarVariant:102444","phenotype":{"types":[{"id":"HP:0000561","label":"Absent eyelashes"}]}},{"entity":"MGI:1857139","phenotype":{"types":[{"id":"MP:0000528","label":"delayed kidney development"}]}},{"entity":"ClinVarVariant:158964","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:49611","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:17384","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:216211","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"MGI:3758075","phenotype":{"types":[{"id":"MP:0000822","label":"abnormal brain ventricle morphology"}]}},{"entity":"ClinVarVariant:29712","phenotype":{"types":[{"id":"HP:0002841","label":"Recurrent fungal infections"}]}},{"entity":"MGI:1857314","phenotype":{"types":[{"id":"MP:0011093","label":"embryonic lethality at implantation, complete penetrance"}]}},{"entity":"ClinVarVariant:217430","phenotype":{"types":[{"id":"HP:0001820","label":"Leukonychia"}]}},{"entity":"MGI:4421830","phenotype":{"types":[{"id":"HP:0012864","label":"Abnormal sperm morphology"}]}},{"entity":"ClinVarVariant:198077","phenotype":{"types":[{"id":"HP:0001638","label":"Cardiomyopathy"}]}},{"entity":"MGI:1857229","phenotype":{"types":[{"id":"MP:0000260","label":"abnormal angiogenesis"}]}},{"entity":"MGI:3806024","phenotype":{"types":[{"id":"HP:0011273","label":"Anisocytosis"}]}},{"entity":"ClinVarVariant:50907","phenotype":{"types":[{"id":"HP:0001043","label":"Prominent scalp veins"}]}},{"entity":"ClinVarVariant:3851","phenotype":{"types":[{"id":"HP:0000787","label":"Nephrolithiasis"}]}},{"entity":"ClinVarVariant:40599","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:9597","phenotype":{"types":[{"id":"HP:0001700","label":"Myocardial necrosis"}]}},{"entity":"ClinVarVariant:39524","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:16287","phenotype":{"types":[{"id":"HP:0001363","label":"Craniosynostosis"}]}},{"entity":"MGI:3663386","phenotype":{"types":[{"id":"MP:0005449","label":"abnormal food intake"}]}},{"entity":"ClinVarVariant:12345","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:11012","phenotype":{"types":[{"id":"HP:0001298","label":"Encephalopathy"}]}},{"entity":"ClinVarVariant:53276","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:53901","phenotype":{"types":[{"id":"HP:0003453","label":"Antineutrophil antibody positivity"}]}},{"entity":"MGI:3811603","phenotype":{"types":[{"id":"HP:0003097","label":"Short femur"}]}},{"entity":"ClinVarVariant:6925","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:11788","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ClinVarVariant:54083","phenotype":{"types":[{"id":"HP:0006536","label":"Obstructive lung disease"}]}},{"entity":"ClinVarVariant:11722","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:210318","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006996-WBRNAi00007928","phenotype":{"types":[{"id":"WBPhenotype:0001168","label":"pseudocleavage absent early emb"}]}},{"entity":"ClinVarVariant:182830","phenotype":{"types":[{"id":"HP:0100587","label":"Abnormality of the preputium"}]}},{"entity":"ClinVarVariant:6165","phenotype":{"types":[{"id":"HP:0006789","label":"Mitochondrial encephalopathy"}]}},{"entity":"dbSNP:rs7903146","phenotype":{"types":[{"id":"HP:0100710","label":"Impulsivity"}]}},{"entity":"ClinVarVariant:24926","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:65048","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:6822","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"MGI:3046573","phenotype":{"types":[{"id":"MP:0011085","label":"postnatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:21278","phenotype":{"types":[{"id":"HP:0001222","label":"Spatulate thumbs"}]}},{"entity":"ClinVarVariant:56227","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:155948","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"dbSNP:rs1027643","phenotype":{"types":[{"id":"HP:0000526","label":"Aniridia"}]}},{"entity":"_:genid1976410","phenotype":{"types":[{"id":"ZP:0000868","label":"abnormal(ly) disrupted convergent extension involved in gastrulation"}]}},{"entity":"ClinVarVariant:8267","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"ClinVarVariant:189559","phenotype":{"types":[{"id":"HP:0011097","label":"Epileptic spasms"}]}},{"entity":"ClinVarVariant:2676","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:3621117","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:159096","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-050306-15-ZDB-MRPHLNO-100618-3","phenotype":{"types":[{"id":"GO:0060538PHENOTYPE","label":"skeletal muscle organ development phenotype"}]}},{"entity":"ClinVarVariant:211646","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:189579","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"ClinVarVariant:126807","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:14052","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"MGI:5563785","phenotype":{"types":[{"id":"MP:0009347","label":"increased trabecular bone thickness"}]}},{"entity":"ClinVarVariant:36083","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:195458","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:4300","phenotype":{"types":[{"id":"HP:0003540","label":"Impaired platelet aggregation"}]}},{"entity":"ClinVarVariant:194115","phenotype":{"types":[{"id":"HP:0000962","label":"Hyperkeratosis"}]}},{"entity":"ClinVarVariant:67967","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:16839","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"MGI:4459093","phenotype":{"types":[{"id":"HP:0010831","label":"Impaired proprioception"}]}},{"entity":"ClinVarVariant:209134","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:178847","phenotype":{"types":[{"id":"HP:0001742","label":"Nasal obstruction"}]}},{"entity":"ClinVarVariant:68699","phenotype":{"types":[{"id":"HP:0100530","label":"Abnormality of calcium-phosphate metabolism"}]}},{"entity":"MGI:1856217","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:189359","phenotype":{"types":[{"id":"HP:0000709","label":"Psychosis"}]}},{"entity":"MGI:3510782","phenotype":{"types":[{"id":"MP:0008699","label":"increased interleukin-4 secretion"}]}},{"entity":"MGI:2447199","phenotype":{"types":[{"id":"MP:0000932","label":"absent notochord"}]}},{"entity":"FlyBase:FBal0207596","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:42079","phenotype":{"types":[{"id":"HP:0002720","label":"IgA deficiency"}]}},{"entity":"ClinVarVariant:143802","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:7622","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"MGI:5295747","phenotype":{"types":[{"id":"HP:0003292","label":"Decreased serum leptin"}]}},{"entity":"ClinVarVariant:884","phenotype":{"types":[{"id":"HP:0002318","label":"Cervical myelopathy"}]}},{"entity":"ClinVarVariant:204096","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"ClinVarVariant:1389","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:94230","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:49530","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:30696","phenotype":{"types":[{"id":"HP:0000256","label":"Macrocephaly"}]}},{"entity":"WormBase:WBVar00146313","phenotype":{"types":[{"id":"WBPhenotype:0000962","label":"level of transgene expression variant"}]}},{"entity":"ClinVarVariant:53294","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ClinVarVariant:53935","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"MGI:3757964","phenotype":{"types":[{"id":"HP:0001719","label":"Double outlet right ventricle"}]}},{"entity":"ClinVarVariant:53738","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:193517","phenotype":{"types":[{"id":"HP:0000992","label":"Cutaneous photosensitivity"}]}},{"entity":"MGI:1857930","phenotype":{"types":[{"id":"HP:0011804","label":"Abnormality of muscle physiology"}]}},{"entity":"ClinVarVariant:68711","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:158339","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:6718","phenotype":{"types":[{"id":"HP:0001908","label":"Hypoplastic anemia"}]}},{"entity":"ClinVarVariant:94139","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"ClinVarVariant:45115","phenotype":{"types":[{"id":"HP:0002859","label":"Rhabdomyosarcoma"}]}},{"entity":"MGI:2678305","phenotype":{"types":[{"id":"MP:0002169","label":"no abnormal phenotype detected"}]}},{"entity":"ClinVarVariant:158974","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:9236","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000067-WBRNAi00085673","phenotype":{"types":[{"id":"WBPhenotype:0001260","label":"oocyte morphology variant"}]}},{"entity":"ClinVarVariant:4262","phenotype":{"types":[{"id":"HP:0005177","label":"Premature arteriosclerosis"}]}},{"entity":"ClinVarVariant:42327","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"dbSNP:rs6729815","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"MGI:3840238","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:65058","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:36091","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:7360","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"ClinVarVariant:5225","phenotype":{"types":[{"id":"HP:0011003","label":"Severe Myopia"}]}},{"entity":"ClinVarVariant:65166","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"MGI:3832033","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"ClinVarVariant:10761","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:210456","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003401-WBRNAi00085349","phenotype":{"types":[{"id":"WBPhenotype:0001944","label":"oocyte number decreased"}]}},{"entity":"ClinVarVariant:42089","phenotype":{"types":[{"id":"HP:0002720","label":"IgA deficiency"}]}},{"entity":"FlyBase:FBal0119169","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:186362","phenotype":{"types":[{"id":"HP:0001908","label":"Hypoplastic anemia"}]}},{"entity":"ClinVarVariant:127417","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:39785","phenotype":{"types":[{"id":"HP:0000772","label":"Abnormality of the ribs"}]}},{"entity":"MGI:1857212","phenotype":{"types":[{"id":"MP:0005458","label":"increased percent body fat/body weight"}]}},{"entity":"ClinVarVariant:143525","phenotype":{"types":[{"id":"HP:0000729","label":"Autistic behavior"}]}},{"entity":"ClinVarVariant:101294","phenotype":{"types":[{"id":"HP:0100689","label":"Decreased corneal thickness"}]}},{"entity":"ClinVarVariant:167361","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"ClinVarVariant:16342","phenotype":{"types":[{"id":"HP:0003811","label":"Neonatal death"}]}},{"entity":"MGI:1857722","phenotype":{"types":[{"id":"MP:0012165","label":"absent neural folds"}]}},{"entity":"ClinVarVariant:159921","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:12023","phenotype":{"types":[{"id":"HP:0010978","label":"Abnormality of immune system physiology"}]}},{"entity":"ZFIN:ZDB-ALT-040929-4","phenotype":{"types":[{"id":"ZP:0000043","label":"abnormal(ly) decreased size eye"}]}},{"entity":"ClinVarVariant:10118","phenotype":{"types":[{"id":"HP:0005542","label":"Prolonged whole-blood clotting time"}]}},{"entity":"MGI:2176049","phenotype":{"types":[{"id":"HP:0002414","label":"Spina bifida"}]}},{"entity":"ClinVarVariant:53923","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:49631","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:36093","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:35890","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"dbSNP:rs109529219","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:8875","phenotype":{"types":[{"id":"HP:0009773","label":"Symphalangism affecting the phalanges of the hand"}]}},{"entity":"MGI:5548830","phenotype":{"types":[{"id":"MP:0010123","label":"increased bone mineral content"}]}},{"entity":"ClinVarVariant:141944","phenotype":{"types":[{"id":"HP:0005374","label":"Cellular immunodeficiency"}]}},{"entity":"ClinVarVariant:40068","phenotype":{"types":[{"id":"HP:0000105","label":"Enlarged kidneys"}]}},{"entity":"ClinVarVariant:7427","phenotype":{"types":[{"id":"HP:0100015","label":"Stahl ear"}]}},{"entity":"MGI:1931521","phenotype":{"types":[{"id":"MP:0005296","label":"abnormal humerus morphology"}]}},{"entity":"ClinVarVariant:10288","phenotype":{"types":[{"id":"HP:0012062","label":"Bone cyst"}]}},{"entity":"FlyBase:FBal0178561","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"MGI:3623277","phenotype":{"types":[{"id":"MP:0003944","label":"abnormal T cell subpopulation ratio"}]}},{"entity":"ClinVarVariant:217280","phenotype":{"types":[{"id":"HP:0006808","label":"Cerebral hypomyelination"}]}},{"entity":"FlyBase:FBal0205457","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"FlyBase:FBal0208360","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:143818","phenotype":{"types":[{"id":"HP:0002376","label":"Developmental regression"}]}},{"entity":"ClinVarVariant:39715","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:210399","phenotype":{"types":[{"id":"HP:0011362","label":"Abnormal hair quantity"}]}},{"entity":"ClinVarVariant:94837","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"MGI:5468252","phenotype":{"types":[{"id":"MP:0011167","label":"abnormal adipose tissue development"}]}},{"entity":"FlyBase:FBal0203318","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:42391","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"ClinVarVariant:333","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"MGI:4360523","phenotype":{"types":[{"id":"MP:0003697","label":"absent zona pellucida"}]}},{"entity":"ClinVarVariant:127329","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:12586","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:217078","phenotype":{"types":[{"id":"HP:0007440","label":"Generalized hyperpigmentation"}]}},{"entity":"ClinVarVariant:54084","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:211656","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"MGI:4939621","phenotype":{"types":[{"id":"MP:0005670","label":"abnormal white adipose tissue physiology"}]}},{"entity":"FlyBase:FBal0260939","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:2267","phenotype":{"types":[{"id":"HP:0100279","label":"Ulcerative colitis"}]}},{"entity":"ClinVarVariant:137984","phenotype":{"types":[{"id":"HP:0000707","label":"Abnormality of the nervous system"}]}},{"entity":"MGI:3810074","phenotype":{"types":[{"id":"MP:0005092","label":"decreased double-positive T cell number"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002299-WBRNAi00078911","phenotype":{"types":[{"id":"WBPhenotype:0000666","label":"ovulation variant"}]}},{"entity":"ClinVarVariant:210464","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:215893","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:41085","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:133628","phenotype":{"types":[{"id":"HP:0002344","label":"Progressive neurologic deterioration"}]}},{"entity":"ClinVarVariant:180354","phenotype":{"types":[{"id":"HP:0002631","label":"Ascending aortic aneurysm"}]}},{"entity":"ClinVarVariant:135745","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:208846","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"MGI:2158692","phenotype":{"types":[{"id":"MP:0002566","label":"abnormal sexual interaction"}]}},{"entity":"MGI:2183240","phenotype":{"types":[{"id":"MP:0006143","label":"increased systemic arterial diastolic blood pressure"}]}},{"entity":"ClinVarVariant:41001","phenotype":{"types":[{"id":"HP:0001376","label":"Limitation of joint mobility"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00021604-WBRNAi00007532","phenotype":{"types":[{"id":"WBPhenotype:0001119","label":"cell cycle slow early emb"}]}},{"entity":"ClinVarVariant:128203","phenotype":{"types":[{"id":"HP:0000520","label":"Proptosis"}]}},{"entity":"ClinVarVariant:9966","phenotype":{"types":[{"id":"HP:0001923","label":"Reticulocytosis"}]}},{"entity":"ClinVarVariant:31190","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"ClinVarVariant:216404","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:120223","phenotype":{"types":[{"id":"HP:0000953","label":"Hyperpigmentation of the skin"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000912-WBRNAi00066508","phenotype":{"types":[{"id":"WBPhenotype:0000061","label":"extended life span"}]}},{"entity":"ClinVarVariant:10259","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:3773724","phenotype":{"types":[{"id":"MP:0001265","label":"decreased body size"}]}},{"entity":"ClinVarVariant:216414","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:53459","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017967-WBRNAi00000357","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:343","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"MGI:2153811","phenotype":{"types":[{"id":"MP:0000035","label":"abnormal membranous labyrinth morphology"}]}},{"entity":"ClinVarVariant:97534","phenotype":{"types":[{"id":"HP:0000999","label":"Pyoderma"}]}},{"entity":"ClinVarVariant:30262","phenotype":{"types":[{"id":"HP:0000546","label":"Retinal degeneration"}]}},{"entity":"ClinVarVariant:56237","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:4784","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:188125","phenotype":{"types":[{"id":"HP:0012539","label":"Non-Hodgkin lymphoma"}]}},{"entity":"ClinVarVariant:50237","phenotype":{"types":[{"id":"HP:0003300","label":"Ovoid vertebral bodies"}]}},{"entity":"ClinVarVariant:100931","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:9993","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:132699","phenotype":{"types":[{"id":"HP:0001161","label":"Hand polydactyly"}]}},{"entity":"FlyBase:FBal0277862","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ZFIN:ZDB-ALT-121128-4","phenotype":{"types":[{"id":"ZP:0002448","label":"abnormal(ly) disorganized retinal outer nuclear layer"}]}},{"entity":"ClinVarVariant:158984","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:5855","phenotype":{"types":[{"id":"HP:0000217","label":"Xerostomia"}]}},{"entity":"ClinVarVariant:14030","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:210007","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"FlyBase:FBal0098633","phenotype":{"types":[{"id":"FBcv:0000364","label":"sterile"}]}},{"entity":"ClinVarVariant:216764","phenotype":{"types":[{"id":"HP:0000256","label":"Macrocephaly"}]}},{"entity":"ClinVarVariant:143828","phenotype":{"types":[{"id":"HP:0002376","label":"Developmental regression"}]}},{"entity":"ClinVarVariant:96607","phenotype":{"types":[{"id":"HP:0010906","label":"Hyperhistidinemia"}]}},{"entity":"MGI:2651830","phenotype":{"types":[{"id":"MP:0001053","label":"abnormal neuromuscular synapse morphology"}]}},{"entity":"ClinVarVariant:88650","phenotype":{"types":[{"id":"HP:0002408","label":"Cerebral arteriovenous malformation"}]}},{"entity":"FlyBase:FBal0304837","phenotype":{"types":[{"id":"FBbt:00001778PHENOTYPE","label":"Drosophila wing disc phenotype"}]}},{"entity":"ClinVarVariant:162493","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:35601","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:1282","phenotype":{"types":[{"id":"HP:0003398","label":"Abnormal synaptic transmission at the neuromuscular junction"}]}},{"entity":"ClinVarVariant:36041","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:21545","phenotype":{"types":[{"id":"HP:0001256","label":"Intellectual disability, mild"}]}},{"entity":"ClinVarVariant:65068","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:13909","phenotype":{"types":[{"id":"HP:0002527","label":"Falls"}]}},{"entity":"ClinVarVariant:162416","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"dbSNP:rs110710505","phenotype":{"types":[{"id":"AQTLTrait:1120","label":"Thurl width"}]}},{"entity":"ClinVarVariant:5867","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:216132","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:142766","phenotype":{"types":[{"id":"HP:0001067","label":"Neurofibromas"}]}},{"entity":"ClinVarVariant:592","phenotype":{"types":[{"id":"HP:0002286","label":"Fair hair"}]}},{"entity":"ClinVarVariant:94437","phenotype":{"types":[{"id":"HP:0001371","label":"Flexion contracture"}]}},{"entity":"ClinVarVariant:13326","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"ClinVarVariant:7726","phenotype":{"types":[{"id":"HP:0000114","label":"Proximal tubulopathy"}]}},{"entity":"MGI:3624262","phenotype":{"types":[{"id":"HP:0000089","label":"Renal hypoplasia"}]}},{"entity":"ClinVarVariant:49932","phenotype":{"types":[{"id":"HP:0006772","label":"Renal angiomyolipoma"}]}},{"entity":"MGI:4262238","phenotype":{"types":[{"id":"GO:0003351PHENOTYPE","label":"epithelial cilium movement phenotype"}]}},{"entity":"ClinVarVariant:65879","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"FlyBase:FBal0297156","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:101115","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"ClinVarVariant:53185","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"ClinVarVariant:209063","phenotype":{"types":[{"id":"HP:0001648","label":"Cor pulmonale"}]}},{"entity":"ClinVarVariant:56283","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:10629","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:127244","phenotype":{"types":[{"id":"HP:0008734","label":"Decreased testicular size"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001102-WBRNAi00067595","phenotype":{"types":[{"id":"WBPhenotype:0000531","label":"organism development variant"}]}},{"entity":"ClinVarVariant:67858","phenotype":{"types":[{"id":"HP:0004756","label":"Ventricular tachycardia"}]}},{"entity":"ClinVarVariant:135922","phenotype":{"types":[{"id":"HP:0002672","label":"Gastrointestinal carcinoma"}]}},{"entity":"ClinVarVariant:35825","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:39594","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:143592","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"MGI:2152978","phenotype":{"types":[{"id":"MP:0004669","label":"enlarged vertebral body"}]}},{"entity":"FlyBase:FBal0210008","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:179260","phenotype":{"types":[{"id":"HP:0000358","label":"Posteriorly rotated ears"}]}},{"entity":"ClinVarVariant:53376","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:40680","phenotype":{"types":[{"id":"HP:0003010","label":"Prolonged bleeding time"}]}},{"entity":"ClinVarVariant:21242","phenotype":{"types":[{"id":"HP:0000202","label":"Oral cleft"}]}},{"entity":"ClinVarVariant:211666","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:3441","phenotype":{"types":[{"id":"HP:0001199","label":"Triphalangeal thumb"}]}},{"entity":"ClinVarVariant:17082","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:159244","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"MGI:2148205","phenotype":{"types":[{"id":"MP:0004236","label":"absent masseter muscle"}]}},{"entity":"ClinVarVariant:9246","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:188766","phenotype":{"types":[{"id":"HP:0000635","label":"Blue irides"}]}},{"entity":"ClinVarVariant:24502","phenotype":{"types":[{"id":"HP:0000099","label":"Glomerulonephritis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00012632-WBRNAi00067998","phenotype":{"types":[{"id":"WBPhenotype:0000531","label":"organism development variant"}]}},{"entity":"ClinVarVariant:24601","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:188938","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"ClinVarVariant:10263","phenotype":{"types":[{"id":"HP:0005681","label":"Juvenile rheumatoid arthritis"}]}},{"entity":"ClinVarVariant:49641","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"MGI:3771975","phenotype":{"types":[{"id":"MP:0000458","label":"abnormal mandible morphology"}]}},{"entity":"MGI:3765956","phenotype":{"types":[{"id":"GO:0042981PHENOTYPE","label":"regulation of apoptotic process phenotype"}]}},{"entity":"ClinVarVariant:18452","phenotype":{"types":[{"id":"HP:0000047","label":"Hypospadias"}]}},{"entity":"ClinVarVariant:29740","phenotype":{"types":[{"id":"HP:0010628","label":"Facial palsy"}]}},{"entity":"ClinVarVariant:216584","phenotype":{"types":[{"id":"HP:0006771","label":"Duodenal adenocarcinoma"}]}},{"entity":"ClinVarVariant:204313","phenotype":{"types":[{"id":"HP:0001989","label":"Fetal akinesia sequence"}]}},{"entity":"ClinVarVariant:4442","phenotype":{"types":[{"id":"HP:0001947","label":"Renal tubular acidosis"}]}},{"entity":"ClinVarVariant:120219","phenotype":{"types":[{"id":"HP:0001055","label":"Erysipelas"}]}},{"entity":"ClinVarVariant:158070","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:93153","phenotype":{"types":[{"id":"HP:0002202","label":"Pleural effusion"}]}},{"entity":"ClinVarVariant:12391","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:97700","phenotype":{"types":[{"id":"HP:0001596","label":"Alopecia"}]}},{"entity":"ClinVarVariant:10832","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"MGI:3778272","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:16646","phenotype":{"types":[{"id":"HP:0007110","label":"Central hypoventilation"}]}},{"entity":"ClinVarVariant:49661","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:24686","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"ClinVarVariant:158186","phenotype":{"types":[{"id":"HP:0011097","label":"Epileptic spasms"}]}},{"entity":"FlyBase:FBal0300880","phenotype":{"types":[{"id":"GO:0005634PHENOTYPE","label":"nucleus phenotype"}]}},{"entity":"ClinVarVariant:25360","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"WormBase:WBVar00144564","phenotype":{"types":[{"id":"WBPhenotype:0000687","label":"feminization of XX and XO animals"}]}},{"entity":"FlyBase:FBal0213074","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:52378","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"MGI:5518726","phenotype":{"types":[{"id":"MP:0000715","label":"decreased thymocyte number"}]}},{"entity":"ClinVarVariant:135736","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"_:genid1974728","phenotype":{"types":[{"id":"ZP:0001828","label":"abnormal(ly) malformed post-vent region"}]}},{"entity":"ClinVarVariant:5095","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"MGI:2183400","phenotype":{"types":[{"id":"MP:0005026","label":"decreased susceptibility to parasitic infection"}]}},{"entity":"ClinVarVariant:16275","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:2180768","phenotype":{"types":[{"id":"HP:0000777","label":"Abnormality of the thymus"}]}},{"entity":"MGI:5449635","phenotype":{"types":[{"id":"MP:0001661","label":"extended life span"}]}},{"entity":"FlyBase:FBal0268099","phenotype":{"types":[{"id":"FBbt:00004508PHENOTYPE","label":"eye phenotype"}]}},{"entity":"ClinVarVariant:3766","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:55941","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:53915","phenotype":{"types":[{"id":"HP:0010943","label":"Echogenic fetal bowel"}]}},{"entity":"ClinVarVariant:126447","phenotype":{"types":[{"id":"HP:0000613","label":"Photophobia"}]}},{"entity":"ClinVarVariant:353","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:211728","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"ClinVarVariant:24518","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:216185","phenotype":{"types":[{"id":"HP:0006744","label":"Adrenocortical carcinoma"}]}},{"entity":"MGI:2384163","phenotype":{"types":[{"id":"MP:0000351","label":"increased cell proliferation"}]}},{"entity":"ClinVarVariant:56687","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"ClinVarVariant:1137","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:36494","phenotype":{"types":[{"id":"HP:0004879","label":"Intermittent hyperventilation"}]}},{"entity":"ClinVarVariant:158994","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:14870","phenotype":{"types":[{"id":"HP:0010049","label":"Short metacarpal"}]}},{"entity":"ClinVarVariant:54013","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:208563","phenotype":{"types":[{"id":"HP:0001397","label":"Hepatic steatosis"}]}},{"entity":"FlyBase:FBal0209552","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:211312","phenotype":{"types":[{"id":"HP:0000445","label":"Wide nose"}]}},{"entity":"ClinVarVariant:13624","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:25335","phenotype":{"types":[{"id":"HP:0012023","label":"Galactosuria"}]}},{"entity":"ClinVarVariant:21575","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:216875","phenotype":{"types":[{"id":"HP:0002247","label":"Duodenal atresia"}]}},{"entity":"ClinVarVariant:41122","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:54094","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:53628","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:53903","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:188883","phenotype":{"types":[{"id":"HP:0001947","label":"Renal tubular acidosis"}]}},{"entity":"ClinVarVariant:101165","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:50106","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"MGI:5588201","phenotype":{"types":[{"id":"MP:0001685","label":"abnormal endoderm development"}]}},{"entity":"ClinVarVariant:30204","phenotype":{"types":[{"id":"HP:0000577","label":"Exotropia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011067-WBRNAi00081161","phenotype":{"types":[{"id":"WBPhenotype:0001569","label":"body wall muscle myosin organization defective"}]}},{"entity":"MGI:2679886","phenotype":{"types":[{"id":"HP:0012535","label":"Abnormal synaptic transmission"}]}},{"entity":"dbSNP:rs7787531","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"ClinVarVariant:179299","phenotype":{"types":[{"id":"HP:0004309","label":"Ventricular preexcitation"}]}},{"entity":"ClinVarVariant:50854","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:53945","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:25205","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:9120","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"ClinVarVariant:135872","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:56595","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"ClinVarVariant:56615","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"FlyBase:FBal0239685","phenotype":{"types":[{"id":"FBbt:00004729PHENOTYPE","label":"Drosophila wing phenotype"}]}},{"entity":"ClinVarVariant:9551","phenotype":{"types":[{"id":"HP:0002401","label":"Stroke-like episodes"}]}},{"entity":"ClinVarVariant:49651","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:110","phenotype":{"types":[{"id":"HP:0002321","label":"Vertigo"}]}},{"entity":"MGI:3054960","phenotype":{"types":[{"id":"MP:0001928","label":"abnormal ovulation"}]}},{"entity":"ClinVarVariant:82640","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:2216","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"ClinVarVariant:4034","phenotype":{"types":[{"id":"HP:0000158","label":"Macroglossia"}]}},{"entity":"ClinVarVariant:8963","phenotype":{"types":[{"id":"HP:0000126","label":"Hydronephrosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002251-WBRNAi00063113","phenotype":{"types":[{"id":"WBPhenotype:0000523","label":"chemical response variant"}]}},{"entity":"AQTL:25943","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:53544","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"FlyBase:FBal0258455","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:189716","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:135929","phenotype":{"types":[{"id":"HP:0100615","label":"Ovarian neoplasm"}]}},{"entity":"ClinVarVariant:39","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:215576","phenotype":{"types":[{"id":"HP:0005550","label":"Chronic lymphatic leukemia"}]}},{"entity":"MGI:1856699","phenotype":{"types":[{"id":"MP:0000376","label":"folliculitis"}]}},{"entity":"ClinVarVariant:127144","phenotype":{"types":[{"id":"HP:0002078","label":"Truncal ataxia"}]}},{"entity":"MGI:1857734","phenotype":{"types":[{"id":"MP:0011084","label":"lethality at weaning, incomplete penetrance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00018892-WBRNAi00000065","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:43612","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:163462","phenotype":{"types":[{"id":"HP:0002097","label":"Emphysema"}]}},{"entity":"FlyBase:FBal0128189","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:4387","phenotype":{"types":[{"id":"HP:0002486","label":"Myotonia"}]}},{"entity":"ClinVarVariant:95023","phenotype":{"types":[{"id":"HP:0007018","label":"Attention deficit hyperactivity disorder"}]}},{"entity":"ClinVarVariant:136194","phenotype":{"types":[{"id":"HP:0000157","label":"Abnormality of the tongue"}]}},{"entity":"ClinVarVariant:25320","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:38921","phenotype":{"types":[{"id":"HP:0001888","label":"Lymphopenia"}]}},{"entity":"ClinVarVariant:101118","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"dbSNP:rs41643216","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:211716","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"MGI:1857212","phenotype":{"types":[{"id":"GO:0030301PHENOTYPE","label":"cholesterol transport phenotype"}]}},{"entity":"ClinVarVariant:40562","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:97035","phenotype":{"types":[{"id":"HP:0000023","label":"Inguinal hernia"}]}},{"entity":"ClinVarVariant:24289","phenotype":{"types":[{"id":"HP:0000613","label":"Photophobia"}]}},{"entity":"AQTL:41940","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:68302","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"dbSNP:rs5219","phenotype":{"types":[{"id":"HP:0001254","label":"Lethargy"}]}},{"entity":"ClinVarVariant:83166","phenotype":{"types":[{"id":"HP:0006740","label":"Transitional cell carcinoma of the bladder"}]}},{"entity":"FlyBase:FBal0205897","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:21164","phenotype":{"types":[{"id":"HP:0002827","label":"Hip dislocation"}]}},{"entity":"FlyBase:FBal0102923","phenotype":{"types":[{"id":"FBbt:00005177PHENOTYPE","label":"Drosophila chaeta phenotype"}]}},{"entity":"MGI:1933748","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:135879","phenotype":{"types":[{"id":"HP:0010767","label":"Sacrococcygeal pilonidal abnormality"}]}},{"entity":"ClinVarVariant:56293","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:35835","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:39071","phenotype":{"types":[{"id":"HP:0009769","label":"Bullet-shaped phalanges of the hand"}]}},{"entity":"MGI:2668394","phenotype":{"types":[{"id":"HP:0002414","label":"Spina bifida"}]}},{"entity":"ClinVarVariant:38377","phenotype":{"types":[{"id":"HP:0002172","label":"Postural instability"}]}},{"entity":"ClinVarVariant:11846","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:53690","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00021829-WBRNAi00004730","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:53794","phenotype":{"types":[{"id":"HP:0100598","label":"Pulmonary edema"}]}},{"entity":"MGI:4948909","phenotype":{"types":[{"id":"MP:0004952","label":"increased spleen weight"}]}},{"entity":"ClinVarVariant:204087","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"MGI:2178475","phenotype":{"types":[{"id":"HP:0011014","label":"Abnormal glucose homeostasis"}]}},{"entity":"ClinVarVariant:132749","phenotype":{"types":[{"id":"HP:0011069","label":"Increased number of teeth"}]}},{"entity":"ClinVarVariant:49681","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"MGI:3530077","phenotype":{"types":[{"id":"MP:0001513","label":"limb grasping"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022017-WBRNAi00090877","phenotype":{"types":[{"id":"WBPhenotype:0002095","label":"lysosome-related organelle morphology variant"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-030131-1213-ZDB-MRPHLNO-131120-6","phenotype":{"types":[{"id":"ZP:0004518","label":"abnormal(ly) immature eye"}]}},{"entity":"ClinVarVariant:14214","phenotype":{"types":[{"id":"HP:0001732","label":"Abnormality of the pancreas"}]}},{"entity":"MGI:2180880","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"ClinVarVariant:216023","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:1855960","phenotype":{"types":[{"id":"MP:0005075","label":"abnormal melanosome morphology"}]}},{"entity":"ClinVarVariant:53370","phenotype":{"types":[{"id":"HP:0000027","label":"Azoospermia"}]}},{"entity":"ClinVarVariant:31851","phenotype":{"types":[{"id":"HP:0000944","label":"Abnormality of the metaphyses"}]}},{"entity":"MGI:1856209","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:3187","phenotype":{"types":[{"id":"HP:0010049","label":"Short metacarpal"}]}},{"entity":"ClinVarVariant:50040","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"ClinVarVariant:190786","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:161239","phenotype":{"types":[{"id":"HP:0007293","label":"Anterior sacral meningocele"}]}},{"entity":"ClinVarVariant:29943","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ZFIN:ZDB-ALT-030919-2","phenotype":{"types":[{"id":"ZP:0009068","label":"abnormal(ly) disrupted spinal cord oligodendrocyte cell differentiation"}]}},{"entity":"FlyBase:FBal0239048","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:14718","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:40186","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:156282","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"MGI:3845227","phenotype":{"types":[{"id":"HP:0005563","label":"Decreased numbers of nephrons"}]}},{"entity":"ClinVarVariant:53858","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"FlyBase:FBal0207413","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:4443","phenotype":{"types":[{"id":"HP:0008682","label":"Acute tubular necrosis"}]}},{"entity":"ClinVarVariant:13503","phenotype":{"types":[{"id":"HP:0002171","label":"Gliosis"}]}},{"entity":"ClinVarVariant:8189","phenotype":{"types":[{"id":"HP:0002196","label":"Myelopathy"}]}},{"entity":"ClinVarVariant:38980","phenotype":{"types":[{"id":"HP:0003458","label":"EMG: myopathic abnormalities"}]}},{"entity":"ClinVarVariant:136167","phenotype":{"types":[{"id":"HP:0001578","label":"Hypercortisolism"}]}},{"entity":"ClinVarVariant:13960","phenotype":{"types":[{"id":"HP:0001640","label":"Cardiomegaly"}]}},{"entity":"ClinVarVariant:21166","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:1333","phenotype":{"types":[{"id":"HP:0000601","label":"Hypotelorism"}]}},{"entity":"MGI:4429385","phenotype":{"types":[{"id":"MP:0001364","label":"decreased anxiety-related response"}]}},{"entity":"ClinVarVariant:53992","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:41462","phenotype":{"types":[{"id":"HP:0000473","label":"Torticollis"}]}},{"entity":"MGI:3716074","phenotype":{"types":[{"id":"MP:0005332","label":"abnormal amino acid level"}]}},{"entity":"ClinVarVariant:180305","phenotype":{"types":[{"id":"HP:0001519","label":"Disproportionate tall stature"}]}},{"entity":"ClinVarVariant:48806","phenotype":{"types":[{"id":"HP:0009720","label":"Adenoma sebaceum"}]}},{"entity":"FlyBase:FBal0183239","phenotype":{"types":[{"id":"FBbt:00005156PHENOTYPE","label":"Drosophila mechanosensory sensory organ phenotype"}]}},{"entity":"ClinVarVariant:49247","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"ClinVarVariant:35753","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"MGI:1931048","phenotype":{"types":[{"id":"MP:0005325","label":"abnormal renal glomerulus morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006917-WBRNAi00040864","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"ClinVarVariant:21779","phenotype":{"types":[{"id":"HP:0002411","label":"Myokymia"}]}},{"entity":"ClinVarVariant:127349","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:21218","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"WormBase:WBVar00143078","phenotype":{"types":[{"id":"WBPhenotype:0001652","label":"anchor cell invasion variant"}]}},{"entity":"ClinVarVariant:49810","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:53356","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:17272","phenotype":{"types":[{"id":"HP:0002273","label":"Tetraparesis"}]}},{"entity":"ClinVarVariant:211467","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:10204","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:6542","phenotype":{"types":[{"id":"HP:0001805","label":"Thick nail"}]}},{"entity":"ClinVarVariant:10822","phenotype":{"types":[{"id":"HP:0002757","label":"Recurrent fractures"}]}},{"entity":"ClinVarVariant:5449","phenotype":{"types":[{"id":"HP:0002671","label":"Basal cell carcinoma"}]}},{"entity":"ClinVarVariant:180392","phenotype":{"types":[{"id":"HP:0011034","label":"Amyloidosis"}]}},{"entity":"ClinVarVariant:5905","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:41187","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004506-WBRNAi00078787","phenotype":{"types":[{"id":"WBPhenotype:0001171","label":"shortened life span"}]}},{"entity":"ClinVarVariant:21451","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:2628","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:50060","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"ClinVarVariant:12965","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:2453","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:210427","phenotype":{"types":[{"id":"HP:0005599","label":"Hypopigmentation of hair"}]}},{"entity":"ClinVarVariant:53863","phenotype":{"types":[{"id":"HP:0010943","label":"Echogenic fetal bowel"}]}},{"entity":"ClinVarVariant:215894","phenotype":{"types":[{"id":"HP:0000012","label":"Urinary urgency"}]}},{"entity":"ClinVarVariant:9714","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"MGI:3836429","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:8061","phenotype":{"types":[{"id":"HP:0006443","label":"Patellar aplasia"}]}},{"entity":"ClinVarVariant:217068","phenotype":{"types":[{"id":"HP:0007440","label":"Generalized hyperpigmentation"}]}},{"entity":"ClinVarVariant:54053","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:209164","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"FlyBase:FBal0195554","phenotype":{"types":[{"id":"FBbt:00001311PHENOTYPE","label":"interface glial cell phenotype"}]}},{"entity":"FlyBase:FBal0209714","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"FlyBase:FBal0091132","phenotype":{"types":[{"id":"FBbt:00004642PHENOTYPE","label":"Drosophila tibia phenotype"}]}},{"entity":"ClinVarVariant:189261","phenotype":{"types":[{"id":"HP:0001284","label":"Areflexia"}]}},{"entity":"ClinVarVariant:10915","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:39848","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"dbSNP:rs110754910","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:93724","phenotype":{"types":[{"id":"HP:0006979","label":"Sleep-wake cycle disturbance"}]}},{"entity":"ClinVarVariant:25231","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"MGI:3656024","phenotype":{"types":[{"id":"MP:0000228","label":"abnormal thrombopoiesis"}]}},{"entity":"ClinVarVariant:5312","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004188-WBRNAi00095757","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:68288","phenotype":{"types":[{"id":"HP:0001874","label":"Abnormality of neutrophils"}]}},{"entity":"ClinVarVariant:53660","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"ClinVarVariant:8184","phenotype":{"types":[{"id":"HP:0003095","label":"Septic arthritis"}]}},{"entity":"ClinVarVariant:30988","phenotype":{"types":[{"id":"HP:0001845","label":"Overlapping toe"}]}},{"entity":"ZFIN:ZDB-ALT-050916-14","phenotype":{"types":[{"id":"ZP:0004993","label":"abnormal(ly) constricted heart"}]}},{"entity":"ClinVarVariant:53943","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"MGI:5466366","phenotype":{"types":[{"id":"MP:0001513","label":"limb grasping"}]}},{"entity":"ClinVarVariant:53935","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:56613","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:183678","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:16879","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:38752","phenotype":{"types":[{"id":"HP:0000519","label":"Congenital cataract"}]}},{"entity":"ClinVarVariant:182386","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:65739","phenotype":{"types":[{"id":"HP:0000691","label":"Microdontia"}]}},{"entity":"ClinVarVariant:53841","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:66439","phenotype":{"types":[{"id":"HP:0011441","label":"Abnormality of the medulla oblongata"}]}},{"entity":"ClinVarVariant:2259","phenotype":{"types":[{"id":"HP:0001287","label":"Meningitis"}]}},{"entity":"ClinVarVariant:1703","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"_:genid1976040","phenotype":{"types":[{"id":"ZP:0002310","label":"abnormal(ly) circling whole organism"}]}},{"entity":"dbSNP:rs12386026","phenotype":{"types":[{"id":"HP:0006516","label":"Hypersensitivity pneumonitis"}]}},{"entity":"MGI:3761621","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:211746","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:158392","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ClinVarVariant:12641","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"MGI:4432238","phenotype":{"types":[{"id":"MP:0004889","label":"increased energy expenditure"}]}},{"entity":"ClinVarVariant:217052","phenotype":{"types":[{"id":"HP:0100697","label":"Neurofibrosarcoma"}]}},{"entity":"ClinVarVariant:11129","phenotype":{"types":[{"id":"HP:0005549","label":"Congenital neutropenia"}]}},{"entity":"ClinVarVariant:56034","phenotype":{"types":[{"id":"HP:0000815","label":"Hypergonadotropic hypogonadism"}]}},{"entity":"ClinVarVariant:6286","phenotype":{"types":[{"id":"HP:0000925","label":"Abnormality of the vertebral column"}]}},{"entity":"ClinVarVariant:9960","phenotype":{"types":[{"id":"HP:0004936","label":"Venous thrombosis"}]}},{"entity":"ClinVarVariant:64779","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"ClinVarVariant:56635","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"MGI:2158457","phenotype":{"types":[{"id":"MP:0000527","label":"abnormal kidney development"}]}},{"entity":"ClinVarVariant:100671","phenotype":{"types":[{"id":"HP:0004719","label":"Hyperechogenic kidneys"}]}},{"entity":"ClinVarVariant:12791","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:101135","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"ClinVarVariant:189852","phenotype":{"types":[{"id":"HP:0002384","label":"Focal seizures with impairment of consciousness or awareness"}]}},{"entity":"AQTL:20678","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:13340","phenotype":{"types":[{"id":"HP:0004808","label":"Acute myeloid leukemia"}]}},{"entity":"ClinVarVariant:40490","phenotype":{"types":[{"id":"HP:0100495","label":"Mastocytosis"}]}},{"entity":"ClinVarVariant:94601","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"WormBase:WBVar00531947","phenotype":{"types":[{"id":"WBPhenotype:0000138","label":"lipid composition variant"}]}},{"entity":"MGI:3712283","phenotype":{"types":[{"id":"MP:0006316","label":"increased urine sodium level"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017983-WBRNAi00075550","phenotype":{"types":[{"id":"WBPhenotype:0000032","label":"sick"}]}},{"entity":"ClinVarVariant:44631","phenotype":{"types":[{"id":"HP:0000179","label":"Thick lower lip vermilion"}]}},{"entity":"MGI:5317762","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"MGI:2153094","phenotype":{"types":[{"id":"HP:0001397","label":"Hepatic steatosis"}]}},{"entity":"MGI:5467564","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:132733","phenotype":{"types":[{"id":"HP:0100777","label":"Exostoses"}]}},{"entity":"ClinVarVariant:53794","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:1568","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:5502","phenotype":{"types":[{"id":"HP:0200094","label":"Frontal open bite"}]}},{"entity":"MGI:3043520","phenotype":{"types":[{"id":"MP:0004952","label":"increased spleen weight"}]}},{"entity":"MGI:2157350","phenotype":{"types":[{"id":"GO:0030900PHENOTYPE","label":"forebrain development phenotype"}]}},{"entity":"ClinVarVariant:17189","phenotype":{"types":[{"id":"HP:0000768","label":"Pectus carinatum"}]}},{"entity":"ClinVarVariant:18025","phenotype":{"types":[{"id":"HP:0004850","label":"Recurrent deep vein thrombosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006975-WBRNAi00081919","phenotype":{"types":[{"id":"WBPhenotype:0001595","label":"somatic transgene silencing variant"}]}},{"entity":"ClinVarVariant:100719","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:9454","phenotype":{"types":[{"id":"HP:0000529","label":"Progressive visual loss"}]}},{"entity":"ClinVarVariant:53366","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004453-WBRNAi00072949","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:204127","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:1236","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"ClinVarVariant:48912","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"ClinVarVariant:8212","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:30180","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007030-WBRNAi00026587","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}}],"schema":"phenopacket-level-1"},"params":{"q":"*:*","fq":"(subject_closure:\"HP:0000739\" AND subject_closure:\"MP:0001363\")","personality":"variant_phenotype","showEmptyFields":false},"name":"Monarch Application","date":"Sun Jun 26 2016 12:07:31 GMT-0700 (PDT)"}
\ No newline at end of file
diff -r 000000000000 -r 850bb90bd667 test-data/phenotypes-for-variants-union.json
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/phenotypes-for-variants-union.json Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,1 @@
+{"phenopacket":{"phenotype_profile":[{"entity":"ClinVarVariant:217207","phenotype":{"types":[{"id":"HP:0010535","label":"Sleep apnea"}]}},{"entity":"FlyBase:FBal0213223","phenotype":{"types":[{"id":"FBcv:0000352","label":"partially lethal - majority die"}]}},{"entity":"ClinVarVariant:11487","phenotype":{"types":[{"id":"HP:0001829","label":"Foot polydactyly"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022219-WBRNAi00094335","phenotype":{"types":[{"id":"WBPhenotype:0000508","label":"nonsense mRNA accumulation"}]}},{"entity":"FlyBase:FBal0204990","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"FlyBase:FBal0094697","phenotype":{"types":[{"id":"FBcv:0000395","label":"locomotor rhythm defective"}]}},{"entity":"ClinVarVariant:126392","phenotype":{"types":[{"id":"HP:0001433","label":"Hepatosplenomegaly"}]}},{"entity":"ClinVarVariant:167486","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:161253","phenotype":{"types":[{"id":"HP:0011096","label":"Peripheral demyelination"}]}},{"entity":"ClinVarVariant:24488","phenotype":{"types":[{"id":"HP:0000517","label":"Abnormality of the lens"}]}},{"entity":"ClinVarVariant:10038","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"ClinVarVariant:120292","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:91630","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:188714","phenotype":{"types":[{"id":"HP:0002015","label":"Dysphagia"}]}},{"entity":"ClinVarVariant:65078","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:13919","phenotype":{"types":[{"id":"HP:0002527","label":"Falls"}]}},{"entity":"ClinVarVariant:166796","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"ClinVarVariant:53300","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:49671","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:6383","phenotype":{"types":[{"id":"HP:0002758","label":"Osteoarthritis"}]}},{"entity":"ClinVarVariant:12869","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:3241","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"MGI:1856875","phenotype":{"types":[{"id":"MP:0000377","label":"abnormal hair follicle morphology"}]}},{"entity":"ClinVarVariant:24448","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"NCBIGene:553991","phenotype":{"types":[{"id":"HP:0003805","label":"Rimmed vacuoles"}]}},{"entity":"ClinVarVariant:35614","phenotype":{"types":[{"id":"HP:0001518","label":"Small for gestational age"}]}},{"entity":"ClinVarVariant:24856","phenotype":{"types":[{"id":"HP:0001636","label":"Tetralogy of Fallot"}]}},{"entity":"ClinVarVariant:135244","phenotype":{"types":[{"id":"HP:0100819","label":"Intestinal fistula"}]}},{"entity":"MGI:3702572","phenotype":{"types":[{"id":"MP:0001327","label":"decreased retinal photoreceptor cell number"}]}},{"entity":"ClinVarVariant:204248","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002981-WBRNAi00083915","phenotype":{"types":[{"id":"WBPhenotype:0001171","label":"shortened life span"}]}},{"entity":"ClinVarVariant:10490","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007201-WBRNAi00062819","phenotype":{"types":[{"id":"WBPhenotype:0000691","label":"gonad development variant"}]}},{"entity":"MGI:2182460","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"dbSNP:rs2202157","phenotype":{"types":[{"id":"HP:0009733","label":"Glioma"}]}},{"entity":"ClinVarVariant:49410","phenotype":{"types":[{"id":"HP:0100764","label":"Lymphangioma"}]}},{"entity":"ClinVarVariant:101209","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"MGI:2684419","phenotype":{"types":[{"id":"MP:0008190","label":"decreased transitional stage B cell number"}]}},{"entity":"MGI:2671609","phenotype":{"types":[{"id":"MP:0011279","label":"decreased ear pigmentation"}]}},{"entity":"ClinVarVariant:215956","phenotype":{"types":[{"id":"HP:0000324","label":"Facial asymmetry"}]}},{"entity":"ClinVarVariant:49985","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"dbSNP:rs1819084","phenotype":{"types":[{"id":"HP:0002721","label":"Immunodeficiency"}]}},{"entity":"ClinVarVariant:42347","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"ClinVarVariant:10746","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"dbSNP:rs10720414","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"ClinVarVariant:100901","phenotype":{"types":[{"id":"HP:0008420","label":"Punctate vertebral calcifications"}]}},{"entity":"ClinVarVariant:40523","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:3975","phenotype":{"types":[{"id":"HP:0000121","label":"Nephrocalcinosis"}]}},{"entity":"ClinVarVariant:191776","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:3243","phenotype":{"types":[{"id":"HP:0001274","label":"Agenesis of corpus callosum"}]}},{"entity":"ClinVarVariant:49691","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:53303","phenotype":{"types":[{"id":"HP:0100732","label":"Pancreatic fibrosis"}]}},{"entity":"MGI:3046930","phenotype":{"types":[{"id":"MP:0008828","label":"abnormal lymph node cell ratio"}]}},{"entity":"ClinVarVariant:10947","phenotype":{"types":[{"id":"HP:0002007","label":"Frontal bossing"}]}},{"entity":"ClinVarVariant:208036","phenotype":{"types":[{"id":"HP:0000280","label":"Coarse facial features"}]}},{"entity":"ClinVarVariant:216123","phenotype":{"types":[{"id":"HP:0001350","label":"Slurred speech"}]}},{"entity":"ClinVarVariant:10634","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"ClinVarVariant:13684","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:53955","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:42536","phenotype":{"types":[{"id":"HP:0001297","label":"Stroke"}]}},{"entity":"dbSNP:rs109157116","phenotype":{"types":[{"id":"AQTLTrait:1067","label":"Length of productive life"}]}},{"entity":"ClinVarVariant:143822","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:208497","phenotype":{"types":[{"id":"HP:0002179","label":"Opisthotonus"}]}},{"entity":"ClinVarVariant:42838","phenotype":{"types":[{"id":"HP:0003712","label":"Skeletal muscle hypertrophy"}]}},{"entity":"ClinVarVariant:53165","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"MGI:2159365","phenotype":{"types":[{"id":"HP:0005528","label":"Bone marrow hypocellularity"}]}},{"entity":"ClinVarVariant:65088","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:40601","phenotype":{"types":[{"id":"HP:0008443","label":"Spinal deformities"}]}},{"entity":"ClinVarVariant:10128","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"MGI:2178049","phenotype":{"types":[{"id":"MP:0001405","label":"impaired coordination"}]}},{"entity":"FlyBase:FBal0294203","phenotype":{"types":[{"id":"FBbt:00001920PHENOTYPE","label":"embryonic/larval brain phenotype"}]}},{"entity":"ClinVarVariant:5007","phenotype":{"types":[{"id":"HP:0001182","label":"Tapered finger"}]}},{"entity":"ClinVarVariant:363","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:184551","phenotype":{"types":[{"id":"HP:0002216","label":"Premature graying of hair"}]}},{"entity":"MGI:3834217","phenotype":{"types":[{"id":"MP:0002841","label":"impaired skeletal muscle contractility"}]}},{"entity":"ClinVarVariant:45379","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:158297","phenotype":{"types":[{"id":"HP:0010761","label":"Broad columella"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004470-WBRNAi00085516","phenotype":{"types":[{"id":"WBPhenotype:0001954","label":"diplotene absent during oogenesis"}]}},{"entity":"ClinVarVariant:7309","phenotype":{"types":[{"id":"HP:0000954","label":"Single transverse palmar crease"}]}},{"entity":"ClinVarVariant:11580","phenotype":{"types":[{"id":"HP:0002007","label":"Frontal bossing"}]}},{"entity":"ClinVarVariant:7057","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:10283","phenotype":{"types":[{"id":"HP:0100710","label":"Impulsivity"}]}},{"entity":"ClinVarVariant:8492","phenotype":{"types":[{"id":"HP:0001332","label":"Dystonia"}]}},{"entity":"MGI:3841488","phenotype":{"types":[{"id":"HP:0004324","label":"Increased body weight"}]}},{"entity":"ClinVarVariant:189720","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"MGI:5140883","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"MGI:2182765","phenotype":{"types":[{"id":"MP:0001257","label":"increased body length"}]}},{"entity":"ClinVarVariant:39667","phenotype":{"types":[{"id":"HP:0001067","label":"Neurofibromas"}]}},{"entity":"ClinVarVariant:690","phenotype":{"types":[{"id":"HP:0010471","label":"Oligosacchariduria"}]}},{"entity":"ClinVarVariant:38952","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:215911","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:143120","phenotype":{"types":[{"id":"HP:0001653","label":"Mitral regurgitation"}]}},{"entity":"ClinVarVariant:159945","phenotype":{"types":[{"id":"HP:0002465","label":"Poor speech"}]}},{"entity":"ClinVarVariant:45183","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"ClinVarVariant:66101","phenotype":{"types":[{"id":"HP:0004469","label":"Chronic bronchitis"}]}},{"entity":"ClinVarVariant:127491","phenotype":{"types":[{"id":"HP:0000377","label":"Abnormality of the pinna"}]}},{"entity":"ClinVarVariant:208829","phenotype":{"types":[{"id":"HP:0009601","label":"Aplasia/Hypoplasia of the thumb"}]}},{"entity":"ClinVarVariant:24772","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:36051","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:158343","phenotype":{"types":[{"id":"HP:0000742","label":"Self-mutilation"}]}},{"entity":"dbSNP:rs10172646","phenotype":{"types":[{"id":"HP:0001931","label":"Hypochromic anemia"}]}},{"entity":"ClinVarVariant:56735","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:162049","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:12595","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"ClinVarVariant:13342","phenotype":{"types":[{"id":"HP:0002861","label":"Melanoma"}]}},{"entity":"ClinVarVariant:184560","phenotype":{"types":[{"id":"HP:0009734","label":"Optic glioma"}]}},{"entity":"ClinVarVariant:5985","phenotype":{"types":[{"id":"HP:0003119","label":"Abnormality of lipid metabolism"}]}},{"entity":"ClinVarVariant:92534","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:17178","phenotype":{"types":[{"id":"HP:0006149","label":"Increased laxity of fingers"}]}},{"entity":"FlyBase:FBal0137361","phenotype":{"types":[{"id":"FBbt:00005634PHENOTYPE","label":"Drosophila embryonic Malpighian tubule phenotype"}]}},{"entity":"ClinVarVariant:99942","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"MGI:1891594","phenotype":{"types":[{"id":"HP:0008222","label":"Female infertility"}]}},{"entity":"ClinVarVariant:53953","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:64885","phenotype":{"types":[{"id":"HP:0003881","label":"Humeral sclerosis"}]}},{"entity":"ClinVarVariant:180352","phenotype":{"types":[{"id":"HP:0002835","label":"Aspiration"}]}},{"entity":"ClinVarVariant:2023","phenotype":{"types":[{"id":"HP:0000830","label":"Anterior hypopituitarism"}]}},{"entity":"ClinVarVariant:94505","phenotype":{"types":[{"id":"HP:0002948","label":"Vertebral fusion"}]}},{"entity":"ClinVarVariant:12048","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"AQTL:20712","phenotype":{"types":[{"id":"AQTLTrait:1114","label":"Body length"}]}},{"entity":"MGI:1932294","phenotype":{"types":[{"id":"HP:0012819","label":"Myocarditis"}]}},{"entity":"ClinVarVariant:12493","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"ClinVarVariant:12589","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:24660","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:48937","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:13960","phenotype":{"types":[{"id":"HP:0002208","label":"Coarse hair"}]}},{"entity":"ClinVarVariant:21062","phenotype":{"types":[{"id":"HP:0000660","label":"Lipemia retinalis"}]}},{"entity":"ClinVarVariant:158712","phenotype":{"types":[{"id":"HP:0009237","label":"Short 5th finger"}]}},{"entity":"ClinVarVariant:11931","phenotype":{"types":[{"id":"HP:0001376","label":"Limitation of joint mobility"}]}},{"entity":"ClinVarVariant:204128","phenotype":{"types":[{"id":"HP:0100758","label":"Gangrene"}]}},{"entity":"ClinVarVariant:35880","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:155757","phenotype":{"types":[{"id":"HP:0001539","label":"Omphalocele"}]}},{"entity":"FlyBase:FBal0298766","phenotype":{"types":[{"id":"FBbt:00007250PHENOTYPE","label":"Drosophila inter-ommatidial cell phenotype"}]}},{"entity":"ClinVarVariant:189801","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"ClinVarVariant:167312","phenotype":{"types":[{"id":"HP:0002027","label":"Abdominal pain"}]}},{"entity":"ClinVarVariant:159955","phenotype":{"types":[{"id":"HP:0002465","label":"Poor speech"}]}},{"entity":"ClinVarVariant:127747","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:373","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"MGI:1861456","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"FlyBase:FBal0150123","phenotype":{"types":[{"id":"FBbt:00004970PHENOTYPE","label":"cuticle phenotype"}]}},{"entity":"FlyBase:FBal0183487","phenotype":{"types":[{"id":"FBcv:0000430","label":"cell polarity defective"}]}},{"entity":"ClinVarVariant:11218","phenotype":{"types":[{"id":"HP:0001685","label":"Myocardial fibrosis"}]}},{"entity":"MGI:5311370","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"ClinVarVariant:10497","phenotype":{"types":[{"id":"HP:0011855","label":"Pharyngeal edema"}]}},{"entity":"ClinVarVariant:53319","phenotype":{"types":[{"id":"HP:0100027","label":"Recurrent pancreatitis"}]}},{"entity":"ClinVarVariant:49838","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:68576","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:10572","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"MGI:4454555","phenotype":{"types":[{"id":"MP:0001745","label":"increased circulating corticosterone level"}]}},{"entity":"ClinVarVariant:97593","phenotype":{"types":[{"id":"HP:0005214","label":"Intestinal obstruction"}]}},{"entity":"ClinVarVariant:161981","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"ClinVarVariant:40512","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:188788","phenotype":{"types":[{"id":"HP:0000649","label":"Abnormality of visual evoked potentials"}]}},{"entity":"ClinVarVariant:10174","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:38289","phenotype":{"types":[{"id":"HP:0002196","label":"Myelopathy"}]}},{"entity":"ClinVarVariant:2334","phenotype":{"types":[{"id":"HP:0001315","label":"Reduced tendon reflexes"}]}},{"entity":"ClinVarVariant:64739","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:177995","phenotype":{"types":[{"id":"HP:0001279","label":"Syncope"}]}},{"entity":"ClinVarVariant:53999","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:181735","phenotype":{"types":[{"id":"HP:0008572","label":"External ear malformation"}]}},{"entity":"ClinVarVariant:11712","phenotype":{"types":[{"id":"HP:0001388","label":"Joint laxity"}]}},{"entity":"ClinVarVariant:38324","phenotype":{"types":[{"id":"HP:0000046","label":"Scrotal hypoplasia"}]}},{"entity":"ClinVarVariant:11077","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:7151","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:9141","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:188928","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:9064","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017241-WBRNAi00096241","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-001103-2-ZDB-MRPHLNO-041110-4-ZDB-MRPHLNO-050322-1","phenotype":{"types":[{"id":"ZP:0000064","label":"abnormal(ly) decreased size ceratohyal cartilage"}]}},{"entity":"ClinVarVariant:40680","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:210726","phenotype":{"types":[{"id":"HP:0001231","label":"Abnormality of the fingernails"}]}},{"entity":"MGI:3584018","phenotype":{"types":[{"id":"HP:0100827","label":"Lymphocytosis"}]}},{"entity":"NCBIGene:100526741","phenotype":{"types":[{"id":"HP:0002823","label":"Abnormality of the femur"}]}},{"entity":"ClinVarVariant:42317","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"ClinVarVariant:12786","phenotype":{"types":[{"id":"HP:0001028","label":"Hemangioma"}]}},{"entity":"MGI:4450934","phenotype":{"types":[{"id":"MP:0002188","label":"small heart"}]}},{"entity":"ClinVarVariant:43594","phenotype":{"types":[{"id":"HP:0002488","label":"Acute leukemia"}]}},{"entity":"ClinVarVariant:211626","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"FlyBase:FBal0206465","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:159239","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:156048","phenotype":{"types":[{"id":"HP:0002270","label":"Abnormality of the autonomic nervous system"}]}},{"entity":"ClinVarVariant:24478","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:40565","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"dbSNP:rs41625970","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:1461","phenotype":{"types":[{"id":"HP:0007359","label":"Focal seizures"}]}},{"entity":"ClinVarVariant:9581","phenotype":{"types":[{"id":"HP:0002401","label":"Stroke-like episodes"}]}},{"entity":"ClinVarVariant:21170","phenotype":{"types":[{"id":"HP:0001511","label":"Intrauterine growth retardation"}]}},{"entity":"ClinVarVariant:189700","phenotype":{"types":[{"id":"HP:0000478","label":"Abnormality of the eye"}]}},{"entity":"ClinVarVariant:14067","phenotype":{"types":[{"id":"HP:0001712","label":"Left ventricular hypertrophy"}]}},{"entity":"ClinVarVariant:49844","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:36848","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:16901","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:100938","phenotype":{"types":[{"id":"HP:0007018","label":"Attention deficit hyperactivity disorder"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000817-WBRNAi00073502","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:46499","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"dbSNP:rs41597892","phenotype":{"types":[{"id":"AQTLTrait:1101","label":"Foot angle"}]}},{"entity":"ClinVarVariant:167132","phenotype":{"types":[{"id":"HP:0000225","label":"Gingival bleeding"}]}},{"entity":"FlyBase:FBal0151927","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"AQTL:33210","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001210-WBRNAi00090496","phenotype":{"types":[{"id":"WBPhenotype:0001645","label":"protein degradation variant"}]}},{"entity":"ClinVarVariant:94504","phenotype":{"types":[{"id":"HP:0008443","label":"Spinal deformities"}]}},{"entity":"ClinVarVariant:4950","phenotype":{"types":[{"id":"HP:0005855","label":"Multiple prenatal fractures"}]}},{"entity":"ClinVarVariant:3331","phenotype":{"types":[{"id":"HP:0001575","label":"Mood changes"}]}},{"entity":"ClinVarVariant:210258","phenotype":{"types":[{"id":"HP:0007360","label":"Aplasia/Hypoplasia of the cerebellum"}]}},{"entity":"ClinVarVariant:101203","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"AQTL:1008","phenotype":{"types":[{"id":"AQTLTrait:3088","label":"Shoulder muscle weight"}]}},{"entity":"ClinVarVariant:24227","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:6011","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:43690","phenotype":{"types":[{"id":"HP:0000268","label":"Dolichocephaly"}]}},{"entity":"FlyBase:FBal0237989","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"MGI:2180062","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:25201","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:142320","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:36061","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:180362","phenotype":{"types":[{"id":"HP:0002835","label":"Aspiration"}]}},{"entity":"MGI:5301308","phenotype":{"types":[{"id":"MP:0004810","label":"decreased hematopoietic stem cell number"}]}},{"entity":"ClinVarVariant:156447","phenotype":{"types":[{"id":"HP:0000138","label":"Ovarian cyst"}]}},{"entity":"ClinVarVariant:10905","phenotype":{"types":[{"id":"HP:0002716","label":"Lymphadenopathy"}]}},{"entity":"ClinVarVariant:94260","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:3282","phenotype":{"types":[{"id":"HP:0009588","label":"Vestibular Schwannoma"}]}},{"entity":"ClinVarVariant:65095","phenotype":{"types":[{"id":"HP:0009727","label":"Achromatic retinal patches"}]}},{"entity":"ClinVarVariant:30186","phenotype":{"types":[{"id":"HP:0100021","label":"Cerebral palsy"}]}},{"entity":"ClinVarVariant:607","phenotype":{"types":[{"id":"HP:0100753","label":"Schizophrenia"}]}},{"entity":"ZFIN:ZDB-ALT-070117-12","phenotype":{"types":[{"id":"ZP:0008988","label":"abnormal(ly) disrupted regulation of hydrogen peroxide metabolic process"}]}},{"entity":"FlyBase:FBal0318121","phenotype":{"types":[{"id":"FBbt:00000015PHENOTYPE","label":"Drosophila thorax phenotype"}]}},{"entity":"ClinVarVariant:9153","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"ClinVarVariant:2240","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"WormBase:WBVar00087821","phenotype":{"types":[{"id":"WBPhenotype:0001384","label":"fertility reduced"}]}},{"entity":"ClinVarVariant:466","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:53630","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:136044","phenotype":{"types":[{"id":"HP:0001587","label":"Primary ovarian failure"}]}},{"entity":"ClinVarVariant:137633","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"MGI:2386179","phenotype":{"types":[{"id":"HP:0012533","label":"Allodynia"}]}},{"entity":"ClinVarVariant:217059","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:137950","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"ClinVarVariant:18045","phenotype":{"types":[{"id":"HP:0004850","label":"Recurrent deep vein thrombosis"}]}},{"entity":"ClinVarVariant:4407","phenotype":{"types":[{"id":"HP:0002200","label":"Pseudobulbar signs"}]}},{"entity":"FlyBase:FBal0045026","phenotype":{"types":[{"id":"FBbt:00004223PHENOTYPE","label":"Drosophila photoreceptor cell R6 phenotype"}]}},{"entity":"ClinVarVariant:36948","phenotype":{"types":[{"id":"HP:0002206","label":"Pulmonary fibrosis"}]}},{"entity":"ClinVarVariant:161343","phenotype":{"types":[{"id":"HP:0001038","label":"Warfarin-induced skin necrosis"}]}},{"entity":"dbSNP:rs6538140","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"MGI:5449877","phenotype":{"types":[{"id":"HP:0002069","label":"Generalized tonic-clonic seizures"}]}},{"entity":"MGI:3845814","phenotype":{"types":[{"id":"MP:0010957","label":"abnormal aerobic respiration"}]}},{"entity":"ClinVarVariant:11369","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:2821","phenotype":{"types":[{"id":"HP:0007074","label":"Thick corpus callosum"}]}},{"entity":"ClinVarVariant:101186","phenotype":{"types":[{"id":"HP:0000387","label":"Absent earlobe"}]}},{"entity":"ClinVarVariant:6059","phenotype":{"types":[{"id":"HP:0003693","label":"Distal amyotrophy"}]}},{"entity":"dbSNP:rs81270306","phenotype":{"types":[{"id":"AQTLTrait:1023","label":"Hindquarter muscle weight"}]}},{"entity":"ClinVarVariant:18277","phenotype":{"types":[{"id":"HP:0002381","label":"Aphasia"}]}},{"entity":"ClinVarVariant:159096","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:41068","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:4394","phenotype":{"types":[{"id":"HP:0000540","label":"Hypermetropia"}]}},{"entity":"ClinVarVariant:12761","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:39786","phenotype":{"types":[{"id":"HP:0000414","label":"Bulbous nose"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004891-WBRNAi00083804","phenotype":{"types":[{"id":"WBPhenotype:0000812","label":"germ cell development variant"}]}},{"entity":"ClinVarVariant:55942","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:35849","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:156130","phenotype":{"types":[{"id":"HP:0010808","label":"Protruding tongue"}]}},{"entity":"FlyBase:FBal0154542","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:35845","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:65098","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:4943","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:41155","phenotype":{"types":[{"id":"HP:0000286","label":"Epicanthus"}]}},{"entity":"ClinVarVariant:10269","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:211718","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"ClinVarVariant:25026","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"ClinVarVariant:37090","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"WormBase:WBVar00248883","phenotype":{"types":[{"id":"WBPhenotype:0001744","label":"cell adhesion variant"}]}},{"entity":"FlyBase:FBal0042573","phenotype":{"types":[{"id":"FBbt:00005744PHENOTYPE","label":"Drosophila embryonic dorsal epidermis phenotype"}]}},{"entity":"ClinVarVariant:64739","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:35723","phenotype":{"types":[{"id":"HP:0000934","label":"Chondrocalcinosis"}]}},{"entity":"ClinVarVariant:94179","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"ClinVarVariant:18333","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"MGI:2156985","phenotype":{"types":[{"id":"MP:0002177","label":"abnormal outer ear morphology"}]}},{"entity":"ClinVarVariant:6717","phenotype":{"types":[{"id":"HP:0001900","label":"Increased hemoglobin"}]}},{"entity":"ClinVarVariant:139529","phenotype":{"types":[{"id":"HP:0000179","label":"Thick lower lip vermilion"}]}},{"entity":"ClinVarVariant:190378","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-040426-2906-ZDB-MRPHLNO-100915-2-ZDB-MRPHLNO-100915-3","phenotype":{"types":[{"id":"ZP:0000962","label":"abnormal(ly) disrupted axonal fasciculation"}]}},{"entity":"ClinVarVariant:189083","phenotype":{"types":[{"id":"HP:0000510","label":"Rod-cone dystrophy"}]}},{"entity":"ClinVarVariant:21255","phenotype":{"types":[{"id":"HP:0002797","label":"Osteolysis"}]}},{"entity":"ClinVarVariant:7215","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:49540","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:209029","phenotype":{"types":[{"id":"HP:0000777","label":"Abnormality of the thymus"}]}},{"entity":"ClinVarVariant:10313","phenotype":{"types":[{"id":"HP:0100309","label":"Subdural hemorrhage"}]}},{"entity":"MGI:5462249","phenotype":{"types":[{"id":"MP:0004532","label":"abnormal inner hair cell stereociliary bundle morphology"}]}},{"entity":"ClinVarVariant:158349","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:12844","phenotype":{"types":[{"id":"HP:0008341","label":"Distal renal tubular acidosis"}]}},{"entity":"FlyBase:FBal0052396","phenotype":{"types":[{"id":"FBbt:00000155PHENOTYPE","label":"Drosophila embryonic head phenotype"}]}},{"entity":"MGI:2180685","phenotype":{"types":[{"id":"MP:0005093","label":"decreased B cell proliferation"}]}},{"entity":"ClinVarVariant:188728","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:10748","phenotype":{"types":[{"id":"HP:0000763","label":"Sensory neuropathy"}]}},{"entity":"ClinVarVariant:24841","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:7750","phenotype":{"types":[{"id":"HP:0012062","label":"Bone cyst"}]}},{"entity":"MGI:4431694","phenotype":{"types":[{"id":"HP:0009887","label":"Abnormality of hair pigmentation"}]}},{"entity":"MGI:3037859","phenotype":{"types":[{"id":"MP:0001394","label":"circling"}]}},{"entity":"ClinVarVariant:40553","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:6927","phenotype":{"types":[{"id":"HP:0004416","label":"Precocious atherosclerosis"}]}},{"entity":"ClinVarVariant:13361","phenotype":{"types":[{"id":"HP:0009830","label":"Peripheral neuropathy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011480-WBRNAi00071460","phenotype":{"types":[{"id":"WBPhenotype:0001425","label":"receptor mediated endocytosis defective"}]}},{"entity":"NCBIGene:100187724","phenotype":{"types":[{"id":"HP:0001161","label":"Hand polydactyly"}]}},{"entity":"ClinVarVariant:189254","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:210769","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:159222","phenotype":{"types":[{"id":"HP:0011951","label":"Aspiration pneumonia"}]}},{"entity":"ClinVarVariant:198999","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"ClinVarVariant:126817","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:189603","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:136156","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:6551","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"ClinVarVariant:128454","phenotype":{"types":[{"id":"HP:0100579","label":"Mucosal telangiectasiae"}]}},{"entity":"ClinVarVariant:93346","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"WormBase:WBVar00090199","phenotype":{"types":[{"id":"WBPhenotype:0001221","label":"nose touch defective"}]}},{"entity":"ClinVarVariant:2141","phenotype":{"types":[{"id":"HP:0009829","label":"Phocomelia"}]}},{"entity":"ClinVarVariant:940","phenotype":{"types":[{"id":"HP:0003053","label":"Epiphyseal deformities of tubular bones"}]}},{"entity":"ClinVarVariant:53705","phenotype":{"types":[{"id":"HP:0004936","label":"Venous thrombosis"}]}},{"entity":"ClinVarVariant:204184","phenotype":{"types":[{"id":"HP:0012622","label":"Chronic kidney disease"}]}},{"entity":"ClinVarVariant:5396","phenotype":{"types":[{"id":"HP:0001655","label":"Patent foramen ovale"}]}},{"entity":"MGI:1934013","phenotype":{"types":[{"id":"MP:0008810","label":"increased circulating iron level"}]}},{"entity":"ClinVarVariant:50009","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:211665","phenotype":{"types":[{"id":"HP:0000413","label":"Atresia of the external auditory canal"}]}},{"entity":"ClinVarVariant:24243","phenotype":{"types":[{"id":"HP:0012622","label":"Chronic kidney disease"}]}},{"entity":"MGI:4836722","phenotype":{"types":[{"id":"HP:0040216","label":"Hypoinsulinemia"}]}},{"entity":"ClinVarVariant:159226","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:143858","phenotype":{"types":[{"id":"HP:0002376","label":"Developmental regression"}]}},{"entity":"FlyBase:FBal0285352","phenotype":{"types":[{"id":"FBbt:00004580PHENOTYPE","label":"Drosophila mesothoracic tergum phenotype"}]}},{"entity":"ClinVarVariant:101219","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:25321","phenotype":{"types":[{"id":"HP:0100626","label":"Chronic hepatic failure"}]}},{"entity":"MGI:3775093","phenotype":{"types":[{"id":"MP:0002052","label":"decreased tumor incidence"}]}},{"entity":"ClinVarVariant:143832","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000201-WBRNAi00088651","phenotype":{"types":[{"id":"WBPhenotype:0002057","label":"Bacillus thuringiensis toxin hypersensitive"}]}},{"entity":"MGI:5295482","phenotype":{"types":[{"id":"HP:0012447","label":"Abnormal myelination"}]}},{"entity":"ClinVarVariant:40243","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:188151","phenotype":{"types":[{"id":"HP:0002894","label":"Neoplasm of the pancreas"}]}},{"entity":"ClinVarVariant:16332","phenotype":{"types":[{"id":"HP:0003811","label":"Neonatal death"}]}},{"entity":"ClinVarVariant:24723","phenotype":{"types":[{"id":"HP:0030034","label":"Diffuse glomerular basement membrane lamellation"}]}},{"entity":"ClinVarVariant:82781","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"MGI:2384028","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:48104","phenotype":{"types":[{"id":"HP:0100272","label":"Branchial sinus"}]}},{"entity":"ClinVarVariant:2666","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:5849","phenotype":{"types":[{"id":"HP:0000684","label":"Delayed eruption of teeth"}]}},{"entity":"MGI:3047571","phenotype":{"types":[{"id":"MP:0008178","label":"decreased germinal center B cell number"}]}},{"entity":"ClinVarVariant:141579","phenotype":{"types":[{"id":"HP:0002216","label":"Premature graying of hair"}]}},{"entity":"ClinVarVariant:6395","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"AQTL:2263","phenotype":{"types":[{"id":"AQTLTrait:2048","label":"Drumstick weight"}]}},{"entity":"ClinVarVariant:158183","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"MGI:3575756","phenotype":{"types":[{"id":"MP:0001874","label":"acanthosis"}]}},{"entity":"ClinVarVariant:53638","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"FlyBase:FBal0297233","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:17494","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:5033","phenotype":{"types":[{"id":"HP:0003477","label":"Peripheral axonal neuropathy"}]}},{"entity":"ClinVarVariant:17370","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:190796","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"MGI:4839367","phenotype":{"types":[{"id":"MP:0009716","label":"abnormal subcommissural organ morphology"}]}},{"entity":"ClinVarVariant:135746","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:188246","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:53626","phenotype":{"types":[{"id":"HP:0006510","label":"Chronic obstructive pulmonary disease"}]}},{"entity":"ClinVarVariant:215765","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:88863","phenotype":{"types":[{"id":"HP:0011108","label":"Recurrent sinusitis"}]}},{"entity":"ClinVarVariant:67956","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:159118","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:21249","phenotype":{"types":[{"id":"HP:0006487","label":"Bowing of the long bones"}]}},{"entity":"ClinVarVariant:207996","phenotype":{"types":[{"id":"HP:0002749","label":"Osteomalacia"}]}},{"entity":"ClinVarVariant:215985","phenotype":{"types":[{"id":"HP:0000612","label":"Iris coloboma"}]}},{"entity":"ClinVarVariant:36081","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:97710","phenotype":{"types":[{"id":"HP:0001596","label":"Alopecia"}]}},{"entity":"FlyBase:FBal0242010","phenotype":{"types":[{"id":"FBbt:00006029PHENOTYPE","label":"Drosophila wing pouch phenotype"}]}},{"entity":"ClinVarVariant:41196","phenotype":{"types":[{"id":"HP:0010535","label":"Sleep apnea"}]}},{"entity":"ClinVarVariant:10136","phenotype":{"types":[{"id":"HP:0005261","label":"Joint hemorrhage"}]}},{"entity":"ClinVarVariant:189623","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"FlyBase:FBal0159231","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:4280","phenotype":{"types":[{"id":"HP:0001053","label":"Hypopigmented skin patches"}]}},{"entity":"ClinVarVariant:65546","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"MGI:1857691","phenotype":{"types":[{"id":"MP:0013216","label":"absent ectoderm"}]}},{"entity":"ClinVarVariant:53178","phenotype":{"types":[{"id":"HP:0100582","label":"Nasal polyposis"}]}},{"entity":"ClinVarVariant:24385","phenotype":{"types":[{"id":"HP:0000093","label":"Proteinuria"}]}},{"entity":"ClinVarVariant:92893","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:21402","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:188745","phenotype":{"types":[{"id":"HP:0001982","label":"Sea-blue histiocytosis"}]}},{"entity":"MGI:1857129","phenotype":{"types":[{"id":"MP:0005386","label":"behavior/neurological phenotype"}]}},{"entity":"ClinVarVariant:159897","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"dbSNP:rs41581462","phenotype":{"types":[{"id":"AQTLTrait:1173","label":"Rear leg set"}]}},{"entity":"ClinVarVariant:41182","phenotype":{"types":[{"id":"HP:0003162","label":"Fasting hypoglycemia"}]}},{"entity":"ClinVarVariant:36062","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:21585","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:210013","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:7112","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:101239","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:41354","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:42353","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"ZFIN:ZDB-ALT-040721-22","phenotype":{"types":[{"id":"ZP:0000100","label":"abnormal(ly) morphology brain"}]}},{"entity":"ClinVarVariant:24444","phenotype":{"types":[{"id":"HP:0007763","label":"Retinal telangiectasia"}]}},{"entity":"MGI:2179136","phenotype":{"types":[{"id":"MP:0006011","label":"abnormal endolymphatic duct morphology"}]}},{"entity":"ClinVarVariant:167477","phenotype":{"types":[{"id":"HP:0005576","label":"Tubulointerstitial fibrosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003834-WBRNAi00040618","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:127355","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"MGI:3609477","phenotype":{"types":[{"id":"MP:0002169","label":"no abnormal phenotype detected"}]}},{"entity":"ClinVarVariant:215464","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"ClinVarVariant:36082","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"MGI:2158467","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:8880","phenotype":{"types":[{"id":"HP:0000863","label":"Central diabetes insipidus"}]}},{"entity":"ClinVarVariant:202211","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ClinVarVariant:48035","phenotype":{"types":[{"id":"HP:0003198","label":"Myopathy"}]}},{"entity":"MGI:1857117","phenotype":{"types":[{"id":"HP:0000961","label":"Cyanosis"}]}},{"entity":"ClinVarVariant:7175","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"MGI:1861705","phenotype":{"types":[{"id":"MP:0000133","label":"abnormal long bone metaphysis morphology"}]}},{"entity":"ZFIN:ZDB-ALT-150203-1","phenotype":{"types":[{"id":"ZP:0012596","label":"abnormal(ly) has extra parts of type compact layer of ventricle basal cortex towards compact layer of ventricle cardiac myofibril"}]}},{"entity":"ClinVarVariant:38975","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:38321","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"FlyBase:FBal0124001","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:143788","phenotype":{"types":[{"id":"HP:0000478","label":"Abnormality of the eye"}]}},{"entity":"ClinVarVariant:36072","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:100921","phenotype":{"types":[{"id":"HP:0007359","label":"Focal seizures"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00016117-WBRNAi00027443","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:211667","phenotype":{"types":[{"id":"HP:0000776","label":"Congenital diaphragmatic hernia"}]}},{"entity":"MGI:2388372","phenotype":{"types":[{"id":"HP:0001941","label":"Acidosis"}]}},{"entity":"ClinVarVariant:190366","phenotype":{"types":[{"id":"HP:0002493","label":"Upper motor neuron dysfunction"}]}},{"entity":"ClinVarVariant:5710","phenotype":{"types":[{"id":"HP:0002179","label":"Opisthotonus"}]}},{"entity":"ClinVarVariant:8470","phenotype":{"types":[{"id":"HP:0003551","label":"Difficulty climbing stairs"}]}},{"entity":"MGI:3775302","phenotype":{"types":[{"id":"HP:0010783","label":"Erythema"}]}},{"entity":"OMIM:242840","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"MGI:4949192","phenotype":{"types":[{"id":"HP:0002242","label":"Abnormality of the intestine"}]}},{"entity":"AQTL:32413","phenotype":{"types":[{"id":"AQTLTrait:1004","label":"Somatic cell count"}]}},{"entity":"ClinVarVariant:66013","phenotype":{"types":[{"id":"HP:0001075","label":"Atrophic scars"}]}},{"entity":"ClinVarVariant:24976","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:31196","phenotype":{"types":[{"id":"HP:0003805","label":"Rimmed vacuoles"}]}},{"entity":"ClinVarVariant:52358","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:162065","phenotype":{"types":[{"id":"HP:0009773","label":"Symphalangism affecting the phalanges of the hand"}]}},{"entity":"ClinVarVariant:197868","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"MGI:2663662","phenotype":{"types":[{"id":"HP:0001875","label":"Neutropenia"}]}},{"entity":"ClinVarVariant:3296","phenotype":{"types":[{"id":"HP:0008069","label":"Neoplasm of the skin"}]}},{"entity":"MGI:4999600","phenotype":{"types":[{"id":"MP:0004971","label":"dermal hyperplasia"}]}},{"entity":"FlyBase:FBal0207033","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:11510","phenotype":{"types":[{"id":"HP:0002938","label":"Lumbar hyperlordosis"}]}},{"entity":"ClinVarVariant:29737","phenotype":{"types":[{"id":"HP:0000602","label":"Ophthalmoplegia"}]}},{"entity":"ClinVarVariant:53902","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00015538-WBRNAi00027160","phenotype":{"types":[{"id":"WBPhenotype:0000697","label":"protruding vulva"}]}},{"entity":"ClinVarVariant:53905","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:36042","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:14889","phenotype":{"types":[{"id":"HP:0008740","label":"Longitudinal vaginal septum"}]}},{"entity":"ClinVarVariant:65064","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"FlyBase:FBal0210388","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:41141","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:10589","phenotype":{"types":[{"id":"HP:0100845","label":"Anaphylactic shock"}]}},{"entity":"ClinVarVariant:12464","phenotype":{"types":[{"id":"HP:0002058","label":"Myopathic facies"}]}},{"entity":"ClinVarVariant:8240","phenotype":{"types":[{"id":"HP:0008947","label":"Infantile muscular hypotonia"}]}},{"entity":"ClinVarVariant:135755","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:210036","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"FlyBase:FBal0240836","phenotype":{"types":[{"id":"FBbt:00004930PHENOTYPE","label":"hub cell phenotype"}]}},{"entity":"dbSNP:rs826221","phenotype":{"types":[{"id":"HP:0002063","label":"Rigidity"}]}},{"entity":"ClinVarVariant:181725","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:161997","phenotype":{"types":[{"id":"HP:0006280","label":"Chronic pancreatitis"}]}},{"entity":"ClinVarVariant:25370","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"dbSNP:rs4869931","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"ClinVarVariant:35870","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"MGI:3530536","phenotype":{"types":[{"id":"MP:0001475","label":"reduced long term depression"}]}},{"entity":"ClinVarVariant:5343","phenotype":{"types":[{"id":"HP:0000968","label":"Ectodermal dysplasia"}]}},{"entity":"MGI:4459078","phenotype":{"types":[{"id":"MP:0010053","label":"decreased grip strength"}]}},{"entity":"ClinVarVariant:132900","phenotype":{"types":[{"id":"HP:0000726","label":"Dementia"}]}},{"entity":"ClinVarVariant:35666","phenotype":{"types":[{"id":"HP:0100530","label":"Abnormality of calcium-phosphate metabolism"}]}},{"entity":"ClinVarVariant:159961","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ClinVarVariant:159118","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"MGI:2154514","phenotype":{"types":[{"id":"HP:0008516","label":"Abnormality of the vertebral spinous processes"}]}},{"entity":"ClinVarVariant:67814","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:840","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:127737","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:24696","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"ClinVarVariant:102431","phenotype":{"types":[{"id":"HP:0001800","label":"Hypoplastic toenails"}]}},{"entity":"MGI:1857257","phenotype":{"types":[{"id":"MP:0008214","label":"increased immature B cell number"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000066-WBRNAi00095708","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:36052","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:11520","phenotype":{"types":[{"id":"HP:0002938","label":"Lumbar hyperlordosis"}]}},{"entity":"ClinVarVariant:163758","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:127415","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:159007","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:9694","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"FlyBase:FBal0305269","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:5616","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:35865","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:43212","phenotype":{"types":[{"id":"HP:0000360","label":"Tinnitus"}]}},{"entity":"ClinVarVariant:24528","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:96387","phenotype":{"types":[{"id":"HP:0100720","label":"Hypoplasia of the ear cartilage"}]}},{"entity":"AQTL:27380","phenotype":{"types":[{"id":"AQTLTrait:1485","label":"Mean corpuscular volume"}]}},{"entity":"ClinVarVariant:156068","phenotype":{"types":[{"id":"HP:0002270","label":"Abnormality of the autonomic nervous system"}]}},{"entity":"ClinVarVariant:210773","phenotype":{"types":[{"id":"HP:0010562","label":"Keloids"}]}},{"entity":"ClinVarVariant:188044","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"FlyBase:FBal0249096","phenotype":{"types":[{"id":"FBbt:00100216PHENOTYPE","label":"dopaminergic PPM1 neuron phenotype"}]}},{"entity":"ClinVarVariant:197559","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:36963","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"dbSNP:rs80879875","phenotype":{"types":[{"id":"AQTLTrait:456","label":"Hemoglobin"}]}},{"entity":"ClinVarVariant:7442","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"MGI:3053810","phenotype":{"types":[{"id":"MP:0002404","label":"increased intestinal adenoma incidence"}]}},{"entity":"ClinVarVariant:190185","phenotype":{"types":[{"id":"HP:0002282","label":"Heterotopia"}]}},{"entity":"ClinVarVariant:138714","phenotype":{"types":[{"id":"HP:0200134","label":"Epileptic encephalopathy"}]}},{"entity":"ClinVarVariant:184231","phenotype":{"types":[{"id":"HP:0001376","label":"Limitation of joint mobility"}]}},{"entity":"ClinVarVariant:2915","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:29732","phenotype":{"types":[{"id":"HP:0002126","label":"Polymicrogyria"}]}},{"entity":"ClinVarVariant:54023","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:143714","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ZFIN:ZDB-ALT-060519-4","phenotype":{"types":[{"id":"ZP:0000041","label":"abnormal(ly) quality pharyngeal arch 3-7 skeleton"}]}},{"entity":"ClinVarVariant:24765","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:2666","phenotype":{"types":[{"id":"HP:0012368","label":"Flat face"}]}},{"entity":"ClinVarVariant:184969","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"ClinVarVariant:7935","phenotype":{"types":[{"id":"HP:0000077","label":"Abnormality of the kidney"}]}},{"entity":"ZFIN:ZDB-ALT-090424-3","phenotype":{"types":[{"id":"ZP:0008370","label":"abnormal(ly) absent gall bladder"}]}},{"entity":"ClinVarVariant:180710","phenotype":{"types":[{"id":"HP:0002151","label":"Increased serum lactate"}]}},{"entity":"ClinVarVariant:8427","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:156391","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:159254","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:31650","phenotype":{"types":[{"id":"HP:0001822","label":"Hallux valgus"}]}},{"entity":"AQTL:20631","phenotype":{"types":[{"id":"AQTLTrait:1112","label":"Withers height"}]}},{"entity":"ClinVarVariant:94585","phenotype":{"types":[{"id":"HP:0002948","label":"Vertebral fusion"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00018782-WBRNAi00099196","phenotype":{"types":[{"id":"WBPhenotype:0000961","label":"pattern of transgene expression variant"}]}},{"entity":"ClinVarVariant:159248","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"ClinVarVariant:160328","phenotype":{"types":[{"id":"HP:0001642","label":"Pulmonic stenosis"}]}},{"entity":"MGI:3832569","phenotype":{"types":[{"id":"MP:0006057","label":"decreased vascular endothelial cell number"}]}},{"entity":"ClinVarVariant:39111","phenotype":{"types":[{"id":"HP:0002721","label":"Immunodeficiency"}]}},{"entity":"ClinVarVariant:9106","phenotype":{"types":[{"id":"HP:0100615","label":"Ovarian neoplasm"}]}},{"entity":"ClinVarVariant:24697","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"MGI:1889550","phenotype":{"types":[{"id":"HP:0003826","label":"Stillbirth"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006768-WBRNAi00071339","phenotype":{"types":[{"id":"WBPhenotype:0000961","label":"pattern of transgene expression variant"}]}},{"entity":"ClinVarVariant:67947","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:53687","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:210474","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:49284","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:10935","phenotype":{"types":[{"id":"HP:0002716","label":"Lymphadenopathy"}]}},{"entity":"ClinVarVariant:13080","phenotype":{"types":[{"id":"HP:0002893","label":"Pituitary adenoma"}]}},{"entity":"_:genid1976017","phenotype":{"types":[{"id":"ZP:0003327","label":"abnormal(ly) disrupted cerebellum development"}]}},{"entity":"ClinVarVariant:189613","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"FlyBase:FBal0199281","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:156327","phenotype":{"types":[{"id":"HP:0006530","label":"Interstitial pulmonary disease"}]}},{"entity":"ClinVarVariant:11352","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"ClinVarVariant:102703","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:40512","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"ClinVarVariant:6433","phenotype":{"types":[{"id":"HP:0001939","label":"Abnormality of metabolism/homeostasis"}]}},{"entity":"ClinVarVariant:49241","phenotype":{"types":[{"id":"HP:0002103","label":"Abnormality of the pleura"}]}},{"entity":"ClinVarVariant:135779","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:56679","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:42900","phenotype":{"types":[{"id":"HP:0003128","label":"Lactic acidosis"}]}},{"entity":"ClinVarVariant:1175","phenotype":{"types":[{"id":"HP:0000013","label":"Hypoplasia of the uterus"}]}},{"entity":"ClinVarVariant:374","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"MGI:3709886","phenotype":{"types":[{"id":"HP:0011014","label":"Abnormal glucose homeostasis"}]}},{"entity":"ClinVarVariant:159181","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"dbSNP:rs29026584","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:65536","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:210471","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:53861","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:29690","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:3231","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"dbSNP:rs1768208","phenotype":{"types":[{"id":"HP:0000658","label":"Eyelid apraxia"}]}},{"entity":"ClinVarVariant:190356","phenotype":{"types":[{"id":"HP:0002493","label":"Upper motor neuron dysfunction"}]}},{"entity":"ClinVarVariant:5353","phenotype":{"types":[{"id":"HP:0001871","label":"Abnormality of blood and blood-forming tissues"}]}},{"entity":"ClinVarVariant:188802","phenotype":{"types":[{"id":"HP:0002487","label":"Hyperkinesis"}]}},{"entity":"ClinVarVariant:49761","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:30471","phenotype":{"types":[{"id":"HP:0004348","label":"Abnormality of bone mineral density"}]}},{"entity":"ClinVarVariant:36032","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-980526-332-ZDB-MRPHLNO-041217-12-ZDB-MRPHLNO-041217-13","phenotype":{"types":[{"id":"ZP:0000027","label":"abnormal(ly) decreased length post-vent region"}]}},{"entity":"ClinVarVariant:7235","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:54083","phenotype":{"types":[{"id":"HP:0000966","label":"Hypohidrosis"}]}},{"entity":"ClinVarVariant:97711","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"ClinVarVariant:159931","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:13090","phenotype":{"types":[{"id":"HP:0002893","label":"Pituitary adenoma"}]}},{"entity":"ClinVarVariant:8120","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:24856","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ClinVarVariant:5825","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:50191","phenotype":{"types":[{"id":"HP:0006772","label":"Renal angiomyolipoma"}]}},{"entity":"ClinVarVariant:2131","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:11161","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"MGI:3579497","phenotype":{"types":[{"id":"GO:0030154PHENOTYPE","label":"cell differentiation phenotype"}]}},{"entity":"AQTL:46070","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:136410","phenotype":{"types":[{"id":"HP:0200040","label":"Epidermoid cyst"}]}},{"entity":"AQTL:5491","phenotype":{"types":[{"id":"AQTLTrait:479","label":"Basophil number"}]}},{"entity":"dbSNP:rs110865743","phenotype":{"types":[{"id":"AQTLTrait:1004","label":"Somatic cell count"}]}},{"entity":"ClinVarVariant:198054","phenotype":{"types":[{"id":"HP:0011712","label":"Right bundle branch block"}]}},{"entity":"ClinVarVariant:13445","phenotype":{"types":[{"id":"HP:0001269","label":"Hemiparesis"}]}},{"entity":"ClinVarVariant:102806","phenotype":{"types":[{"id":"HP:0003231","label":"Hypertyrosinemia"}]}},{"entity":"ClinVarVariant:2657","phenotype":{"types":[{"id":"HP:0006101","label":"Finger syndactyly"}]}},{"entity":"ClinVarVariant:42307","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"ClinVarVariant:158297","phenotype":{"types":[{"id":"HP:0009911","label":"Abnormality of the temporal bone"}]}},{"entity":"ClinVarVariant:128211","phenotype":{"types":[{"id":"HP:0002488","label":"Acute leukemia"}]}},{"entity":"ClinVarVariant:9290","phenotype":{"types":[{"id":"HP:0002063","label":"Rigidity"}]}},{"entity":"ClinVarVariant:188893","phenotype":{"types":[{"id":"HP:0001947","label":"Renal tubular acidosis"}]}},{"entity":"ClinVarVariant:16788","phenotype":{"types":[{"id":"HP:0001274","label":"Agenesis of corpus callosum"}]}},{"entity":"MGI:2384513","phenotype":{"types":[{"id":"MP:0013184","label":"hemorrhagic ascites"}]}},{"entity":"AQTL:50226","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004460-WBRNAi00085472","phenotype":{"types":[{"id":"WBPhenotype:0001948","label":"diakinesis progression during oogenesis variant"}]}},{"entity":"ClinVarVariant:159180","phenotype":{"types":[{"id":"HP:0011951","label":"Aspiration pneumonia"}]}},{"entity":"FlyBase:FBal0040484","phenotype":{"types":[{"id":"FBbt:00004510PHENOTYPE","label":"Drosophila ommatidium phenotype"}]}},{"entity":"ClinVarVariant:8942","phenotype":{"types":[{"id":"HP:0100843","label":"Glioblastoma"}]}},{"entity":"ClinVarVariant:10100","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"MGI:3722325","phenotype":{"types":[{"id":"HP:0010772","label":"Anomalous pulmonary venous return"}]}},{"entity":"ClinVarVariant:49728","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:192299","phenotype":{"types":[{"id":"HP:0030034","label":"Diffuse glomerular basement membrane lamellation"}]}},{"entity":"ClinVarVariant:21101","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"ClinVarVariant:101229","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:10624","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"ClinVarVariant:12870","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:53975","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:6121","phenotype":{"types":[{"id":"HP:0003537","label":"Hypouricemia"}]}},{"entity":"MGI:1856173","phenotype":{"types":[{"id":"MP:0006030","label":"abnormal otic vesicle development"}]}},{"entity":"MGI:1857278","phenotype":{"types":[{"id":"HP:0000110","label":"Renal dysplasia"}]}},{"entity":"ClinVarVariant:212733","phenotype":{"types":[{"id":"HP:0100783","label":"Breast aplasia"}]}},{"entity":"ClinVarVariant:1902","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"ClinVarVariant:186916","phenotype":{"types":[{"id":"HP:0002858","label":"Meningioma"}]}},{"entity":"ClinVarVariant:94841","phenotype":{"types":[{"id":"HP:0003713","label":"Muscle fiber necrosis"}]}},{"entity":"ZFIN:ZDB-ALT-980520-19","phenotype":{"types":[{"id":"ZP:0000406","label":"abnormal(ly) quality sensory system"}]}},{"entity":"ClinVarVariant:9591","phenotype":{"types":[{"id":"HP:0002401","label":"Stroke-like episodes"}]}},{"entity":"ClinVarVariant:65859","phenotype":{"types":[{"id":"HP:0001182","label":"Tapered finger"}]}},{"entity":"ClinVarVariant:83189","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"ClinVarVariant:41057","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:64708","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"ClinVarVariant:209","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:182730","phenotype":{"types":[{"id":"HP:0003189","label":"Long nose"}]}},{"entity":"ClinVarVariant:41023","phenotype":{"types":[{"id":"HP:0009027","label":"Foot dorsiflexor weakness"}]}},{"entity":"ClinVarVariant:127338","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"ClinVarVariant:49450","phenotype":{"types":[{"id":"HP:0009719","label":"Hypomelanotic macule"}]}},{"entity":"ClinVarVariant:190346","phenotype":{"types":[{"id":"HP:0002493","label":"Upper motor neuron dysfunction"}]}},{"entity":"ClinVarVariant:3852","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"MGI:3779080","phenotype":{"types":[{"id":"MP:0010955","label":"abnormal respiratory electron transport chain"}]}},{"entity":"ClinVarVariant:216221","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:40563","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:35855","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"MGI:5635433","phenotype":{"types":[{"id":"MP:0004799","label":"increased susceptibility to experimental autoimmune encephalomyelitis"}]}},{"entity":"ClinVarVariant:24381","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"ClinVarVariant:35868","phenotype":{"types":[{"id":"HP:0100027","label":"Recurrent pancreatitis"}]}},{"entity":"ClinVarVariant:127830","phenotype":{"types":[{"id":"HP:0100585","label":"Telangiectasia of the skin"}]}},{"entity":"ClinVarVariant:143704","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ClinVarVariant:194332","phenotype":{"types":[{"id":"HP:0001350","label":"Slurred speech"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006944-WBRNAi00063314","phenotype":{"types":[{"id":"WBPhenotype:0000697","label":"protruding vulva"}]}},{"entity":"ClinVarVariant:3968","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"MGI:2677631","phenotype":{"types":[{"id":"HP:0010831","label":"Impaired proprioception"}]}},{"entity":"ClinVarVariant:4417","phenotype":{"types":[{"id":"HP:0002200","label":"Pseudobulbar signs"}]}},{"entity":"ClinVarVariant:53996","phenotype":{"types":[{"id":"HP:0010444","label":"Pulmonary insufficiency"}]}},{"entity":"ClinVarVariant:53726","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:25179","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:128201","phenotype":{"types":[{"id":"HP:0002488","label":"Acute leukemia"}]}},{"entity":"ClinVarVariant:207995","phenotype":{"types":[{"id":"HP:0002148","label":"Hypophosphatemia"}]}},{"entity":"MGI:5447471","phenotype":{"types":[{"id":"HP:0003097","label":"Short femur"}]}},{"entity":"ClinVarVariant:194115","phenotype":{"types":[{"id":"HP:0000232","label":"Everted lower lip vermilion"}]}},{"entity":"FlyBase:FBal0245644","phenotype":{"types":[{"id":"FBbt:00005378PHENOTYPE","label":"wing margin phenotype"}]}},{"entity":"FlyBase:FBal0125399","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:159093","phenotype":{"types":[{"id":"HP:0009937","label":"Facial hirsutism"}]}},{"entity":"ClinVarVariant:36093","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:209200","phenotype":{"types":[{"id":"HP:0002126","label":"Polymicrogyria"}]}},{"entity":"ClinVarVariant:12662","phenotype":{"types":[{"id":"HP:0000963","label":"Thin skin"}]}},{"entity":"ClinVarVariant:17247","phenotype":{"types":[{"id":"HP:0000772","label":"Abnormality of the ribs"}]}},{"entity":"ClinVarVariant:1589","phenotype":{"types":[{"id":"HP:0000140","label":"Abnormality of the menstrual cycle"}]}},{"entity":"ClinVarVariant:143113","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:6982","phenotype":{"types":[{"id":"HP:0002553","label":"Highly arched eyebrow"}]}},{"entity":"MGI:3711006","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:60534","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:143554","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"ClinVarVariant:56304","phenotype":{"types":[{"id":"HP:0001562","label":"Oligohydramnios"}]}},{"entity":"ClinVarVariant:10771","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:135886","phenotype":{"types":[{"id":"HP:0200042","label":"Skin ulcer"}]}},{"entity":"ClinVarVariant:101395","phenotype":{"types":[{"id":"HP:0005293","label":"Venous insufficiency"}]}},{"entity":"ClinVarVariant:38580","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"ClinVarVariant:10663","phenotype":{"types":[{"id":"HP:0005542","label":"Prolonged whole-blood clotting time"}]}},{"entity":"FlyBase:FBal0210316","phenotype":{"types":[{"id":"FBbt:00005149PHENOTYPE","label":"ganglion mother cell phenotype"}]}},{"entity":"ClinVarVariant:24412","phenotype":{"types":[{"id":"HP:0011508","label":"Macular hole"}]}},{"entity":"ClinVarVariant:4452","phenotype":{"types":[{"id":"HP:0001947","label":"Renal tubular acidosis"}]}},{"entity":"ClinVarVariant:156058","phenotype":{"types":[{"id":"HP:0002270","label":"Abnormality of the autonomic nervous system"}]}},{"entity":"ClinVarVariant:209163","phenotype":{"types":[{"id":"HP:0011220","label":"Prominent forehead"}]}},{"entity":"ClinVarVariant:7995","phenotype":{"types":[{"id":"HP:0002984","label":"Hypoplasia of the radius"}]}},{"entity":"ClinVarVariant:102626","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:10639","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"MGI:1856088","phenotype":{"types":[{"id":"MP:0006069","label":"abnormal retinal neuronal layer morphology"}]}},{"entity":"ClinVarVariant:7225","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:140867","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:36071","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:40370","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:11034","phenotype":{"types":[{"id":"HP:0001106","label":"Periorbital hyperpigmentation"}]}},{"entity":"ClinVarVariant:17219","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"MGI:3808477","phenotype":{"types":[{"id":"MP:0004920","label":"increased placenta weight"}]}},{"entity":"MGI:2183509","phenotype":{"types":[{"id":"MP:0004411","label":"decreased endocochlear potential"}]}},{"entity":"FlyBase:FBal0294937","phenotype":{"types":[{"id":"FBcv:0000440","label":"chemical sensitive"}]}},{"entity":"MGI:1857225","phenotype":{"types":[{"id":"MP:0004417","label":"decreased cochlear nerve compound action potential"}]}},{"entity":"ClinVarVariant:29700","phenotype":{"types":[{"id":"HP:0005900","label":"Fifth metacarpal with ulnar notch"}]}},{"entity":"ClinVarVariant:13070","phenotype":{"types":[{"id":"HP:0002893","label":"Pituitary adenoma"}]}},{"entity":"ClinVarVariant:21441","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:7179","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050103-13-ZDB-MRPHLNO-120727-1","phenotype":{"types":[{"id":"ZP:0002751","label":"abnormal(ly) hemorrhagic cranial vasculature"}]}},{"entity":"ClinVarVariant:211839","phenotype":{"types":[{"id":"HP:0007359","label":"Focal seizures"}]}},{"entity":"ClinVarVariant:65511","phenotype":{"types":[{"id":"HP:0002066","label":"Gait ataxia"}]}},{"entity":"ClinVarVariant:4465","phenotype":{"types":[{"id":"HP:0000988","label":"Skin rash"}]}},{"entity":"MGI:3852440","phenotype":{"types":[{"id":"MP:0010589","label":"common truncal valve"}]}},{"entity":"ClinVarVariant:195052","phenotype":{"types":[{"id":"HP:0004280","label":"Irregular ossification of hand bones"}]}},{"entity":"ClinVarVariant:56495","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:97701","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"ClinVarVariant:143714","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:2677647","phenotype":{"types":[{"id":"MP:0011088","label":"neonatal lethality, incomplete penetrance"}]}},{"entity":"ClinVarVariant:13396","phenotype":{"types":[{"id":"HP:0001260","label":"Dysarthria"}]}},{"entity":"ClinVarVariant:159973","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"ClinVarVariant:30664","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:31028","phenotype":{"types":[{"id":"HP:0010307","label":"Stridor"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006416-WBRNAi00095532","phenotype":{"types":[{"id":"WBPhenotype:0000402","label":"avoids bacterial lawn"}]}},{"entity":"ClinVarVariant:186867","phenotype":{"types":[{"id":"HP:0002073","label":"Progressive cerebellar ataxia"}]}},{"entity":"ClinVarVariant:11708","phenotype":{"types":[{"id":"HP:0008388","label":"Abnormality of the toenails"}]}},{"entity":"ClinVarVariant:36642","phenotype":{"types":[{"id":"HP:0004308","label":"Ventricular arrhythmia"}]}},{"entity":"ClinVarVariant:8965","phenotype":{"types":[{"id":"HP:0006561","label":"Lipid accumulation in hepatocytes"}]}},{"entity":"ClinVarVariant:25194","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:529","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"ClinVarVariant:156088","phenotype":{"types":[{"id":"HP:0002270","label":"Abnormality of the autonomic nervous system"}]}},{"entity":"ClinVarVariant:6111","phenotype":{"types":[{"id":"HP:0003537","label":"Hypouricemia"}]}},{"entity":"ClinVarVariant:189781","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ClinVarVariant:53484","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:53922","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"_:genid1976433","phenotype":{"types":[{"id":"ZP:0007732","label":"abnormal(ly) decreased amount skeletal muscle cell Z disc"}]}},{"entity":"ClinVarVariant:6718","phenotype":{"types":[{"id":"HP:0100587","label":"Abnormality of the preputium"}]}},{"entity":"ClinVarVariant:35755","phenotype":{"types":[{"id":"HP:0000137","label":"Abnormality of the ovary"}]}},{"entity":"ClinVarVariant:50081","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:1216","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"ClinVarVariant:137994","phenotype":{"types":[{"id":"HP:0000707","label":"Abnormality of the nervous system"}]}},{"entity":"ClinVarVariant:7142","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:10462","phenotype":{"types":[{"id":"HP:0003651","label":"Foam cells"}]}},{"entity":"ClinVarVariant:12063","phenotype":{"types":[{"id":"HP:0008321","label":"Reduced factor X activity"}]}},{"entity":"ClinVarVariant:2468","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:95939","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:39712","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004197-WBRNAi00007235","phenotype":{"types":[{"id":"WBPhenotype:0001263","label":"peroxisome morphology variant"}]}},{"entity":"ClinVarVariant:65124","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:215578","phenotype":{"types":[{"id":"HP:0008348","label":"Immunoglobulin IgG2 deficiency"}]}},{"entity":"ClinVarVariant:156238","phenotype":{"types":[{"id":"HP:0000496","label":"Abnormality of eye movement"}]}},{"entity":"ClinVarVariant:10279","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"AQTL:49858","phenotype":{"types":[{"id":"AQTLTrait:1004","label":"Somatic cell count"}]}},{"entity":"ClinVarVariant:48885","phenotype":{"types":[{"id":"HP:0100764","label":"Lymphangioma"}]}},{"entity":"FlyBase:FBal0236318","phenotype":{"types":[{"id":"FBbt:00000034PHENOTYPE","label":"Drosophila egg phenotype"}]}},{"entity":"ClinVarVariant:634","phenotype":{"types":[{"id":"HP:0004395","label":"Malnutrition"}]}},{"entity":"ClinVarVariant:6094","phenotype":{"types":[{"id":"HP:0006989","label":"Dysplastic corpus callosum"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001093-WBRNAi00026282","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:1932","phenotype":{"types":[{"id":"HP:0006573","label":"Acute hepatic steatosis"}]}},{"entity":"ClinVarVariant:2239","phenotype":{"types":[{"id":"HP:0001287","label":"Meningitis"}]}},{"entity":"ClinVarVariant:2020","phenotype":{"types":[{"id":"HP:0000992","label":"Cutaneous photosensitivity"}]}},{"entity":"ClinVarVariant:42391","phenotype":{"types":[{"id":"HP:0100775","label":"Dural ectasia"}]}},{"entity":"ClinVarVariant:48971","phenotype":{"types":[{"id":"HP:0009594","label":"Retinal hamartoma"}]}},{"entity":"MGI:1857149","phenotype":{"types":[{"id":"MP:0001191","label":"abnormal skin condition"}]}},{"entity":"ClinVarVariant:199656","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"ClinVarVariant:2824","phenotype":{"types":[{"id":"HP:0000297","label":"Facial hypotonia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022042-WBRNAi00081339","phenotype":{"types":[{"id":"WBPhenotype:0001027","label":"nuclear position defective early emb"}]}},{"entity":"ClinVarVariant:53705","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"MGI:4437094","phenotype":{"types":[{"id":"MP:0003059","label":"decreased insulin secretion"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004738-WBRNAi00065884","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:94537","phenotype":{"types":[{"id":"HP:0100595","label":"Camptocormia"}]}},{"entity":"ClinVarVariant:53663","phenotype":{"types":[{"id":"HP:0100651","label":"Type I diabetes mellitus"}]}},{"entity":"ClinVarVariant:136120","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:162048","phenotype":{"types":[{"id":"HP:0009830","label":"Peripheral neuropathy"}]}},{"entity":"ClinVarVariant:49800","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:39534","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:183820","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"MGI:1857227","phenotype":{"types":[{"id":"MP:0001921","label":"reduced fertility"}]}},{"entity":"ClinVarVariant:54030","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"ClinVarVariant:204016","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:2276","phenotype":{"types":[{"id":"HP:0002936","label":"Distal sensory impairment"}]}},{"entity":"ClinVarVariant:25211","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"MGI:2675121","phenotype":{"types":[{"id":"MP:0010979","label":"small ureteric bud"}]}},{"entity":"ClinVarVariant:11544","phenotype":{"types":[{"id":"HP:0006145","label":"Central Y-shaped metacarpal"}]}},{"entity":"ClinVarVariant:38302","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:161353","phenotype":{"types":[{"id":"HP:0001038","label":"Warfarin-induced skin necrosis"}]}},{"entity":"ClinVarVariant:5539","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"MGI:3583735","phenotype":{"types":[{"id":"MP:0000968","label":"abnormal sensory neuron innervation pattern"}]}},{"entity":"ClinVarVariant:11634","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"ZFIN:ZDB-ALT-050916-14","phenotype":{"types":[{"id":"ZP:0000530","label":"abnormal(ly) collapsed dorsal aorta"}]}},{"entity":"MGI:2156622","phenotype":{"types":[{"id":"MP:0001853","label":"heart inflammation"}]}},{"entity":"MGI:3578655","phenotype":{"types":[{"id":"GO:0021636PHENOTYPE","label":"trigeminal nerve morphogenesis phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004915-WBRNAi00075315","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:41172","phenotype":{"types":[{"id":"HP:0003162","label":"Fasting hypoglycemia"}]}},{"entity":"FlyBase:FBal0190540","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:5425","phenotype":{"types":[{"id":"HP:0004927","label":"Pulmonary artery dilatation"}]}},{"entity":"ClinVarVariant:36305","phenotype":{"types":[{"id":"HP:0001025","label":"Urticaria"}]}},{"entity":"ClinVarVariant:158359","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:53265","phenotype":{"types":[{"id":"HP:0011850","label":"Parotitis"}]}},{"entity":"ClinVarVariant:92564","phenotype":{"types":[{"id":"HP:0012702","label":"Tenesmus"}]}},{"entity":"ClinVarVariant:180310","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:212733","phenotype":{"types":[{"id":"HP:0003220","label":"Abnormality of chromosome stability"}]}},{"entity":"ClinVarVariant:17282","phenotype":{"types":[{"id":"HP:0004277","label":"Fractured hand bones"}]}},{"entity":"ClinVarVariant:41078","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:6935","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ZFIN:ZDB-ALT-060602-2","phenotype":{"types":[{"id":"ZP:0006118","label":"abnormal(ly) dilated enterocyte Golgi apparatus"}]}},{"entity":"ClinVarVariant:67937","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:204591","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"MGI:1856893","phenotype":{"types":[{"id":"HP:0012447","label":"Abnormal myelination"}]}},{"entity":"ClinVarVariant:101249","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:49468","phenotype":{"types":[{"id":"HP:0004755","label":"Supraventricular tachycardia"}]}},{"entity":"ClinVarVariant:157677","phenotype":{"types":[{"id":"HP:0008527","label":"Congenital sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:7132","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"MGI:3770133","phenotype":{"types":[{"id":"HP:0000618","label":"Blindness"}]}},{"entity":"ClinVarVariant:210023","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"MGI:2181380","phenotype":{"types":[{"id":"HP:0000029","label":"Testicular atrophy"}]}},{"entity":"ClinVarVariant:215572","phenotype":{"types":[{"id":"HP:0100242","label":"Sarcoma"}]}},{"entity":"ClinVarVariant:101405","phenotype":{"types":[{"id":"HP:0000963","label":"Thin skin"}]}},{"entity":"ClinVarVariant:2145","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"ClinVarVariant:53774","phenotype":{"types":[{"id":"HP:0011109","label":"Chronic sinusitis"}]}},{"entity":"ClinVarVariant:206816","phenotype":{"types":[{"id":"HP:0005484","label":"Postnatal microcephaly"}]}},{"entity":"ClinVarVariant:39442","phenotype":{"types":[{"id":"HP:0007333","label":"Hypoplasia of the frontal lobes"}]}},{"entity":"ClinVarVariant:6050","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:56814","phenotype":{"types":[{"id":"HP:0002676","label":"Cloverleaf skull"}]}},{"entity":"ClinVarVariant:3652","phenotype":{"types":[{"id":"HP:0002028","label":"Chronic diarrhea"}]}},{"entity":"MGI:3512077","phenotype":{"types":[{"id":"MP:0009419","label":"skeletal muscle fibrosis"}]}},{"entity":"ClinVarVariant:4954","phenotype":{"types":[{"id":"HP:0002315","label":"Headache"}]}},{"entity":"ClinVarVariant:101394","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:9219","phenotype":{"types":[{"id":"HP:0011157","label":"Auras"}]}},{"entity":"ClinVarVariant:3861","phenotype":{"types":[{"id":"HP:0000787","label":"Nephrolithiasis"}]}},{"entity":"ZFIN:ZDB-ALT-070309-1","phenotype":{"types":[{"id":"ZP:0010305","label":"abnormal(ly) decreased size atrioventricular canal"}]}},{"entity":"ClinVarVariant:197075","phenotype":{"types":[{"id":"HP:0000431","label":"Wide nasal bridge"}]}},{"entity":"ClinVarVariant:3612","phenotype":{"types":[{"id":"HP:0007819","label":"Presenile cataracts"}]}},{"entity":"ClinVarVariant:11340","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000912-WBRNAi00087983","phenotype":{"types":[{"id":"WBPhenotype:0001171","label":"shortened life span"}]}},{"entity":"ClinVarVariant:101155","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:53995","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:8663","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:10209","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:216067","phenotype":{"types":[{"id":"HP:0009736","label":"Tibial pseudoarthrosis"}]}},{"entity":"ClinVarVariant:211630","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00020051-WBRNAi00095700","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:18336","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:180210","phenotype":{"types":[{"id":"HP:0000974","label":"Hyperextensible skin"}]}},{"entity":"ClinVarVariant:10614","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"WormBase:WBVar00087953","phenotype":{"types":[{"id":"WBPhenotype:0001350","label":"protein phosphorylation increased"}]}},{"entity":"ClinVarVariant:189643","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:2119","phenotype":{"types":[{"id":"HP:0000174","label":"Abnormality of the palate"}]}},{"entity":"MGI:2148547","phenotype":{"types":[{"id":"MP:0006042","label":"increased apoptosis"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-110805-2-ZDB-MRPHLNO-111102-4","phenotype":{"types":[{"id":"ZP:0004922","label":"abnormal(ly) malformed neurohypophysis vasculature"}]}},{"entity":"ClinVarVariant:53748","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:208543","phenotype":{"types":[{"id":"HP:0001344","label":"Absent speech"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019481-WBRNAi00063437","phenotype":{"types":[{"id":"WBPhenotype:0000436","label":"protein subcellular localization variant"}]}},{"entity":"ClinVarVariant:53402","phenotype":{"types":[{"id":"HP:0001948","label":"Alkalosis"}]}},{"entity":"ClinVarVariant:35860","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:50235","phenotype":{"types":[{"id":"HP:0000322","label":"Short philtrum"}]}},{"entity":"ClinVarVariant:1068","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:127727","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:53640","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"MGI:1856656","phenotype":{"types":[{"id":"HP:0001254","label":"Lethargy"}]}},{"entity":"ClinVarVariant:46464","phenotype":{"types":[{"id":"HP:0000738","label":"Hallucinations"}]}},{"entity":"ClinVarVariant:54091","phenotype":{"types":[{"id":"HP:0011034","label":"Amyloidosis"}]}},{"entity":"ClinVarVariant:3221","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:159157","phenotype":{"types":[{"id":"HP:0100627","label":"Displacement of the external urethral meatus"}]}},{"entity":"ZFIN:ZDB-ALT-011017-8","phenotype":{"types":[{"id":"ZP:0013971","label":"abnormal(ly) disrupted caudal fin morphogenesis"}]}},{"entity":"ClinVarVariant:53714","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:16932","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:3157","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:216196","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:194808","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:101213","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"ClinVarVariant:46601","phenotype":{"types":[{"id":"HP:0003327","label":"Axial muscle weakness"}]}},{"entity":"ClinVarVariant:2139","phenotype":{"types":[{"id":"HP:0000089","label":"Renal hypoplasia"}]}},{"entity":"FlyBase:FBal0135890","phenotype":{"types":[{"id":"FBcv:0000411","label":"visual behavior defective"}]}},{"entity":"ClinVarVariant:126827","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:120272","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:200129","phenotype":{"types":[{"id":"HP:0001166","label":"Arachnodactyly"}]}},{"entity":"ClinVarVariant:198695","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:3773644","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"ClinVarVariant:53866","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:161355","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:13372","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004953-WBRNAi00038543","phenotype":{"types":[{"id":"WBPhenotype:0000034","label":"embryonic polarity variant"}]}},{"entity":"ClinVarVariant:56485","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:53446","phenotype":{"types":[{"id":"HP:0006538","label":"Recurrent bronchopulmonary infections"}]}},{"entity":"WormBase:WBVar00251819","phenotype":{"types":[{"id":"WBPhenotype:0000142","label":"cell stress response variant"}]}},{"entity":"ClinVarVariant:24866","phenotype":{"types":[{"id":"HP:0001636","label":"Tetralogy of Fallot"}]}},{"entity":"ClinVarVariant:4274","phenotype":{"types":[{"id":"HP:0000235","label":"Abnormality of the fontanelles or cranial sutures"}]}},{"entity":"ClinVarVariant:31695","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"FlyBase:FBal0151492","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:35875","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:36091","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"MGI:5438282","phenotype":{"types":[{"id":"MP:0005169","label":"abnormal male meiosis"}]}},{"entity":"dbSNP:rs109463474","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:21170","phenotype":{"types":[{"id":"HP:0001518","label":"Small for gestational age"}]}},{"entity":"MGI:3790794","phenotype":{"types":[{"id":"MP:0001302","label":"eyelids open at birth"}]}},{"entity":"ClinVarVariant:189730","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:182720","phenotype":{"types":[{"id":"HP:0003189","label":"Long nose"}]}},{"entity":"ClinVarVariant:53226","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:12995","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:53963","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:194320","phenotype":{"types":[{"id":"HP:0100689","label":"Decreased corneal thickness"}]}},{"entity":"ClinVarVariant:93888","phenotype":{"types":[{"id":"HP:0000311","label":"Round face"}]}},{"entity":"FlyBase:FBal0210205","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"MGI:1857326","phenotype":{"types":[{"id":"HP:0002251","label":"Aganglionic megacolon"}]}},{"entity":"ClinVarVariant:10350","phenotype":{"types":[{"id":"HP:0006380","label":"Knee flexion contracture"}]}},{"entity":"ClinVarVariant:53209","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"FlyBase:FBal0039464","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:11075","phenotype":{"types":[{"id":"HP:0100709","label":"Reduction of oligodendroglia"}]}},{"entity":"ClinVarVariant:10138","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"ClinVarVariant:39425","phenotype":{"types":[{"id":"HP:0003127","label":"Hypocalciuria"}]}},{"entity":"ClinVarVariant:35848","phenotype":{"types":[{"id":"HP:0006516","label":"Hypersensitivity pneumonitis"}]}},{"entity":"NCBIGene:791085","phenotype":{"types":[{"id":"HP:0000337","label":"Broad forehead"}]}},{"entity":"ClinVarVariant:49939","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"ClinVarVariant:30528","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"dbSNP:rs1819084","phenotype":{"types":[{"id":"HP:0002028","label":"Chronic diarrhea"}]}},{"entity":"FlyBase:FBal0219831","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:10868","phenotype":{"types":[{"id":"HP:0008572","label":"External ear malformation"}]}},{"entity":"ClinVarVariant:8267","phenotype":{"types":[{"id":"HP:0001082","label":"Cholecystitis"}]}},{"entity":"FlyBase:FBal0177466","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:11228","phenotype":{"types":[{"id":"HP:0001685","label":"Myocardial fibrosis"}]}},{"entity":"ClinVarVariant:159936","phenotype":{"types":[{"id":"HP:0040082","label":"Happy demeanor"}]}},{"entity":"ClinVarVariant:100921","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:45126","phenotype":{"types":[{"id":"HP:0002047","label":"Malignant hyperthermia"}]}},{"entity":"ClinVarVariant:12816","phenotype":{"types":[{"id":"HP:0008417","label":"Vertebral hypoplasia"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-070410-133-ZDB-MRPHLNO-130620-1","phenotype":{"types":[{"id":"ZP:0008698","label":"abnormal(ly) increased accumulation nucleate erythrocyte towards dorsal aorta"}]}},{"entity":"ClinVarVariant:127459","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"FlyBase:FBal0205974","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:163152","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:30999","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:101142","phenotype":{"types":[{"id":"HP:0000490","label":"Deeply set eye"}]}},{"entity":"FlyBase:FBal0198779","phenotype":{"types":[{"id":"FBbt:00005169PHENOTYPE","label":"Drosophila trichogen cell phenotype"}]}},{"entity":"ClinVarVariant:15644","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:210300","phenotype":{"types":[{"id":"HP:0000457","label":"Depressed nasal ridge"}]}},{"entity":"MGI:1857444","phenotype":{"types":[{"id":"GO:0045765PHENOTYPE","label":"regulation of angiogenesis phenotype"}]}},{"entity":"ClinVarVariant:49232","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:21410","phenotype":{"types":[{"id":"HP:0002069","label":"Generalized tonic-clonic seizures"}]}},{"entity":"ClinVarVariant:39727","phenotype":{"types":[{"id":"HP:0002910","label":"Elevated hepatic transaminases"}]}},{"entity":"ClinVarVariant:49105","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:53985","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:140517","phenotype":{"types":[{"id":"HP:0004540","label":"Congenital, generalized hypertrichosis"}]}},{"entity":"MGI:1933758","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:40522","phenotype":{"types":[{"id":"HP:0000276","label":"Long face"}]}},{"entity":"ClinVarVariant:4234","phenotype":{"types":[{"id":"HP:0010935","label":"Abnormality of the upper urinary tract"}]}},{"entity":"ClinVarVariant:36294","phenotype":{"types":[{"id":"HP:0000832","label":"Primary hypothyroidism"}]}},{"entity":"ClinVarVariant:65623","phenotype":{"types":[{"id":"HP:0001159","label":"Syndactyly"}]}},{"entity":"ClinVarVariant:8379","phenotype":{"types":[{"id":"HP:0003097","label":"Short femur"}]}},{"entity":"ClinVarVariant:3323","phenotype":{"types":[{"id":"HP:0008998","label":"Pectoralis hypoplasia"}]}},{"entity":"ClinVarVariant:41190","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:188880","phenotype":{"types":[{"id":"HP:0002835","label":"Aspiration"}]}},{"entity":"ClinVarVariant:36092","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:126948","phenotype":{"types":[{"id":"HP:0002435","label":"Meningocele"}]}},{"entity":"_:genid1972400","phenotype":{"types":[{"id":"ZP:0003234","label":"abnormal(ly) disrupted glomerular filtration"}]}},{"entity":"MGI:4361278","phenotype":{"types":[{"id":"HP:0003081","label":"Increased urinary potassium"}]}},{"entity":"ClinVarVariant:67539","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:53704","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"FlyBase:FBal0202908","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"MGI:1856241","phenotype":{"types":[{"id":"HP:0000134","label":"Female hypogonadism"}]}},{"entity":"WormBase:WBVar00144142","phenotype":{"types":[{"id":"WBPhenotype:0000229","label":"small"}]}},{"entity":"ClinVarVariant:210437","phenotype":{"types":[{"id":"HP:0005599","label":"Hypopigmentation of hair"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011043-WBRNAi00071240","phenotype":{"types":[{"id":"WBPhenotype:0001425","label":"receptor mediated endocytosis defective"}]}},{"entity":"MGI:3528447","phenotype":{"types":[{"id":"HP:0003138","label":"Increased blood urea nitrogen (BUN)"}]}},{"entity":"AQTL:37488","phenotype":{"types":[{"id":"AQTLTrait:1310","label":"Rabies antibody titer"}]}},{"entity":"ClinVarVariant:49163","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00020347-WBRNAi00072072","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:7178","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:45358","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"MGI:3581891","phenotype":{"types":[{"id":"MP:0004560","label":"abnormal chorionic plate morphology"}]}},{"entity":"ClinVarVariant:91610","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:30207","phenotype":{"types":[{"id":"HP:0011682","label":"Perimembranous ventricular septal defect"}]}},{"entity":"ClinVarVariant:210299","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007400-WBRNAi00080157","phenotype":{"types":[{"id":"ZP:0000676","label":"abnormal(ly) increased rate cell proliferation"}]}},{"entity":"FlyBase:FBal0258532","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:21168","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:158731","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:4889","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:3772","phenotype":{"types":[{"id":"HP:0001022","label":"Albinism"}]}},{"entity":"ClinVarVariant:49905","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:68266","phenotype":{"types":[{"id":"HP:0030273","label":"Reduced red cell adenosine deaminase activity"}]}},{"entity":"ClinVarVariant:5626","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:2446","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:9666","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:135716","phenotype":{"types":[{"id":"HP:0007649","label":"Congenital hypertrophy of retinal pigment epithelium"}]}},{"entity":"ClinVarVariant:190195","phenotype":{"types":[{"id":"HP:0002282","label":"Heterotopia"}]}},{"entity":"ClinVarVariant:42750","phenotype":{"types":[{"id":"HP:0002067","label":"Bradykinesia"}]}},{"entity":"ClinVarVariant:4335","phenotype":{"types":[{"id":"HP:0000751","label":"Personality changes"}]}},{"entity":"ClinVarVariant:204258","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:135754","phenotype":{"types":[{"id":"HP:0012539","label":"Non-Hodgkin lymphoma"}]}},{"entity":"MGI:1934195","phenotype":{"types":[{"id":"MP:0011089","label":"perinatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:35822","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"ClinVarVariant:101128","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"MGI:1856223","phenotype":{"types":[{"id":"HP:0000925","label":"Abnormality of the vertebral column"}]}},{"entity":"MGI:3848796","phenotype":{"types":[{"id":"MP:0001606","label":"impaired hematopoiesis"}]}},{"entity":"ClinVarVariant:13540","phenotype":{"types":[{"id":"HP:0001873","label":"Thrombocytopenia"}]}},{"entity":"dbSNP:rs110180463","phenotype":{"types":[{"id":"AQTLTrait:1289","label":"Milk beta-lactoglobulin protein content"}]}},{"entity":"ZFIN:ZDB-ALT-011017-8","phenotype":{"types":[{"id":"ZP:0003184","label":"abnormal(ly) aplastic dorsal longitudinal anastomotic vessel"}]}},{"entity":"MGI:2182093","phenotype":{"types":[{"id":"HP:0003323","label":"Progressive muscle weakness"}]}},{"entity":"ClinVarVariant:177941","phenotype":{"types":[{"id":"HP:0006579","label":"Prolonged neonatal jaundice"}]}},{"entity":"AQTL:5527","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:132740","phenotype":{"types":[{"id":"HP:0001578","label":"Hypercortisolism"}]}},{"entity":"ClinVarVariant:101400","phenotype":{"types":[{"id":"HP:0000790","label":"Hematuria"}]}},{"entity":"ClinVarVariant:65771","phenotype":{"types":[{"id":"HP:0002013","label":"Vomiting"}]}},{"entity":"ClinVarVariant:101174","phenotype":{"types":[{"id":"HP:0100718","label":"Uterine rupture"}]}},{"entity":"FlyBase:FBal0058990","phenotype":{"types":[{"id":"FBbt:00004508PHENOTYPE","label":"eye phenotype"}]}},{"entity":"ClinVarVariant:21502","phenotype":{"types":[{"id":"HP:0001374","label":"Congenital hip dislocation"}]}},{"entity":"ClinVarVariant:100735","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:186986","phenotype":{"types":[{"id":"HP:0002858","label":"Meningioma"}]}},{"entity":"ClinVarVariant:190262","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:56575","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"ClinVarVariant:181737","phenotype":{"types":[{"id":"HP:0009909","label":"Uplifted earlobe"}]}},{"entity":"ClinVarVariant:39095","phenotype":{"types":[{"id":"HP:0030148","label":"Heart murmur"}]}},{"entity":"ClinVarVariant:211726","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:53912","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:10184","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:56603","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:24285","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"ClinVarVariant:189633","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:25330","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:38497","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"MGI:2387580","phenotype":{"types":[{"id":"MP:0002896","label":"abnormal bone mineralization"}]}},{"entity":"ClinVarVariant:36082","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:193484","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"FlyBase:FBal0213151","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:42357","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"ClinVarVariant:6929","phenotype":{"types":[{"id":"HP:0000660","label":"Lipemia retinalis"}]}},{"entity":"ClinVarVariant:132708","phenotype":{"types":[{"id":"HP:0100242","label":"Sarcoma"}]}},{"entity":"AQTL:34784","phenotype":{"types":[{"id":"AQTLTrait:1326","label":"Milk pentadecylic acid percentage"}]}},{"entity":"ClinVarVariant:211636","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"ClinVarVariant:49721","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:10858","phenotype":{"types":[{"id":"HP:0001290","label":"Generalized hypotonia"}]}},{"entity":"ClinVarVariant:21458","phenotype":{"types":[{"id":"HP:0002511","label":"Alzheimer disease"}]}},{"entity":"MGI:4459519","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:12985","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:49995","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"ClinVarVariant:99928","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:67700","phenotype":{"types":[{"id":"HP:0006682","label":"Ventricular extrasystoles"}]}},{"entity":"ClinVarVariant:17093","phenotype":{"types":[{"id":"HP:0100615","label":"Ovarian neoplasm"}]}},{"entity":"MGI:3611770","phenotype":{"types":[{"id":"MP:0004043","label":"abnormal pH regulation"}]}},{"entity":"ClinVarVariant:10604","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"ClinVarVariant:159928","phenotype":{"types":[{"id":"HP:0001939","label":"Abnormality of metabolism/homeostasis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00009365-WBRNAi00002028","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:135765","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:67966","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:38752","phenotype":{"types":[{"id":"HP:0010741","label":"Edema of the lower limbs"}]}},{"entity":"ClinVarVariant:190261","phenotype":{"types":[{"id":"HP:0100699","label":"Scarring"}]}},{"entity":"ClinVarVariant:215580","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:15443","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"ClinVarVariant:143754","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ClinVarVariant:53204","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:39769","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:204046","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:53564","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"MGI:2152962","phenotype":{"types":[{"id":"MP:0003984","label":"embryonic growth retardation"}]}},{"entity":"ClinVarVariant:4800","phenotype":{"types":[{"id":"HP:0002754","label":"Osteomyelitis"}]}},{"entity":"ClinVarVariant:68716","phenotype":{"types":[{"id":"HP:0007109","label":"Periventricular cysts"}]}},{"entity":"ClinVarVariant:126966","phenotype":{"types":[{"id":"HP:0009713","label":"Spinal hemangioblastoma"}]}},{"entity":"ClinVarVariant:158339","phenotype":{"types":[{"id":"HP:0000343","label":"Long philtrum"}]}},{"entity":"ClinVarVariant:18035","phenotype":{"types":[{"id":"HP:0004850","label":"Recurrent deep vein thrombosis"}]}},{"entity":"ClinVarVariant:94804","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:188862","phenotype":{"types":[{"id":"HP:0002487","label":"Hyperkinesis"}]}},{"entity":"ClinVarVariant:12799","phenotype":{"types":[{"id":"HP:0000133","label":"Gonadal dysgenesis"}]}},{"entity":"ClinVarVariant:10163","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"ClinVarVariant:30294","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:159097","phenotype":{"types":[{"id":"HP:0005815","label":"Supernumerary ribs"}]}},{"entity":"ClinVarVariant:41245","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"ClinVarVariant:3196","phenotype":{"types":[{"id":"HP:0003411","label":"Proximal femoral metaphyseal irregularity"}]}},{"entity":"ClinVarVariant:13567","phenotype":{"types":[{"id":"HP:0000132","label":"Menorrhagia"}]}},{"entity":"ClinVarVariant:41132","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00077526-WBRNAi00070047","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:3813","phenotype":{"types":[{"id":"HP:0004332","label":"Abnormality of lymphocytes"}]}},{"entity":"ClinVarVariant:53734","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"_:genid1976152","phenotype":{"types":[{"id":"ZP:0001609","label":"abnormal(ly) morphology head"}]}},{"entity":"ClinVarVariant:68264","phenotype":{"types":[{"id":"HP:0002644","label":"Abnormality of pelvic girdle bone morphology"}]}},{"entity":"ClinVarVariant:8542","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:53935","phenotype":{"types":[{"id":"HP:0100512","label":"Vitamin D deficiency"}]}},{"entity":"ClinVarVariant:534","phenotype":{"types":[{"id":"HP:0000597","label":"Ophthalmoparesis"}]}},{"entity":"ClinVarVariant:9177","phenotype":{"types":[{"id":"HP:0000384","label":"Preauricular skin tag"}]}},{"entity":"ClinVarVariant:3684","phenotype":{"types":[{"id":"HP:0001114","label":"Xanthelasma"}]}},{"entity":"ClinVarVariant:94605","phenotype":{"types":[{"id":"HP:0002948","label":"Vertebral fusion"}]}},{"entity":"FlyBase:FBal0203313","phenotype":{"types":[{"id":"FBcv:0000352","label":"partially lethal - majority die"}]}},{"entity":"ClinVarVariant:211625","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"MGI:1861958","phenotype":{"types":[{"id":"MP:0009684","label":"abnormal spinal cord lateral motor column morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001746-WBRNAi00084506","phenotype":{"types":[{"id":"WBPhenotype:0001235","label":"cell division polarity variant"}]}},{"entity":"ClinVarVariant:2074","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:189159","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:1033","phenotype":{"types":[{"id":"HP:0003103","label":"Abnormal cortical bone morphology"}]}},{"entity":"ClinVarVariant:6834","phenotype":{"types":[{"id":"HP:0003422","label":"Vertebral segmentation defect"}]}},{"entity":"ClinVarVariant:2076","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"FlyBase:FBal0260715","phenotype":{"types":[{"id":"FBbt:00100529PHENOTYPE","label":"Drosophila embryonic/larval carpet glial cell phenotype"}]}},{"entity":"ClinVarVariant:7994","phenotype":{"types":[{"id":"HP:0009777","label":"Absent thumb"}]}},{"entity":"dbSNP:rs41649184","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:158353","phenotype":{"types":[{"id":"HP:0000742","label":"Self-mutilation"}]}},{"entity":"ClinVarVariant:21535","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:49711","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:35850","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"MGI:3847254","phenotype":{"types":[{"id":"MP:0008237","label":"abnormal ventral coat pigmentation"}]}},{"entity":"ClinVarVariant:36970","phenotype":{"types":[{"id":"HP:0007925","label":"Lacrimal duct aplasia"}]}},{"entity":"ClinVarVariant:13455","phenotype":{"types":[{"id":"HP:0001269","label":"Hemiparesis"}]}},{"entity":"ClinVarVariant:24427","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"ClinVarVariant:24538","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:6051","phenotype":{"types":[{"id":"HP:0100864","label":"Short femoral neck"}]}},{"entity":"ClinVarVariant:7172","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:197156","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:10756","phenotype":{"types":[{"id":"HP:0009830","label":"Peripheral neuropathy"}]}},{"entity":"ClinVarVariant:24299","phenotype":{"types":[{"id":"HP:0000613","label":"Photophobia"}]}},{"entity":"ClinVarVariant:24458","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:93896","phenotype":{"types":[{"id":"HP:0003236","label":"Elevated serum creatine phosphokinase"}]}},{"entity":"ClinVarVariant:159941","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:12403","phenotype":{"types":[{"id":"HP:0009727","label":"Achromatic retinal patches"}]}},{"entity":"ClinVarVariant:10713","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"dbSNP:rs12294076","phenotype":{"types":[{"id":"HP:0002102","label":"Pleuritis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011944-WBRNAi00072116","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"MGI:5615712","phenotype":{"types":[{"id":"MP:0020001","label":"decreased response to antigen"}]}},{"entity":"ClinVarVariant:67927","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:24498","phenotype":{"types":[{"id":"HP:0000517","label":"Abnormality of the lens"}]}},{"entity":"ClinVarVariant:31879","phenotype":{"types":[{"id":"HP:0001712","label":"Left ventricular hypertrophy"}]}},{"entity":"ClinVarVariant:12880","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:49701","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:54093","phenotype":{"types":[{"id":"HP:0004401","label":"Meconium ileus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00013532-WBRNAi00058395","phenotype":{"types":[{"id":"WBPhenotype:0000056","label":"late larval arrest"}]}},{"entity":"ZFIN:ZDB-ALT-150528-4","phenotype":{"types":[{"id":"ZP:0012747","label":"abnormal(ly) process quality cranial neural crest neural crest cell migration"}]}},{"entity":"ClinVarVariant:197759","phenotype":{"types":[{"id":"HP:0005107","label":"Abnormality of the sacrum"}]}},{"entity":"ClinVarVariant:8711","phenotype":{"types":[{"id":"HP:0001895","label":"Normochromic anemia"}]}},{"entity":"ClinVarVariant:196933","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:31592","phenotype":{"types":[{"id":"HP:0003034","label":"Diaphyseal sclerosis"}]}},{"entity":"ClinVarVariant:6221","phenotype":{"types":[{"id":"HP:0100335","label":"Non-midline cleft lip"}]}},{"entity":"ClinVarVariant:210043","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"MGI:3809665","phenotype":{"types":[{"id":"MP:0004946","label":"abnormal regulatory T cell physiology"}]}},{"entity":"ClinVarVariant:1569","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"_:genid1976482","phenotype":{"types":[{"id":"ZP:0010599","label":"abnormal(ly) position ceratohyal cartilage"}]}},{"entity":"ClinVarVariant:210790","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"MGI:3583779","phenotype":{"types":[{"id":"MP:0012113","label":"decreased inner cell mass proliferation"}]}},{"entity":"ClinVarVariant:56697","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"NCBIGene:1165","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:54033","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:210476","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"ClinVarVariant:204036","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:2236","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"MGI:1857189","phenotype":{"types":[{"id":"MP:0008211","label":"decreased mature B cell number"}]}},{"entity":"ClinVarVariant:35895","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:10110","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"ClinVarVariant:189153","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:36511","phenotype":{"types":[{"id":"HP:0002633","label":"Vasculitis"}]}},{"entity":"ClinVarVariant:135748","phenotype":{"types":[{"id":"HP:0008348","label":"Immunoglobulin IgG2 deficiency"}]}},{"entity":"MGI:3815539","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:5419","phenotype":{"types":[{"id":"HP:0002150","label":"Hypercalciuria"}]}},{"entity":"MGI:2668901","phenotype":{"types":[{"id":"MP:0002655","label":"abnormal keratinocyte morphology"}]}},{"entity":"ClinVarVariant:156349","phenotype":{"types":[{"id":"HP:0000227","label":"Tongue telangiectasia"}]}},{"entity":"ClinVarVariant:159039","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:29639","phenotype":{"types":[{"id":"HP:0000689","label":"Dental malocclusion"}]}},{"entity":"ClinVarVariant:297","phenotype":{"types":[{"id":"HP:0001873","label":"Thrombocytopenia"}]}},{"entity":"dbSNP:rs132692798","phenotype":{"types":[{"id":"AQTLTrait:1327","label":"Milk odd-chain fatty acid percentage"}]}},{"entity":"ClinVarVariant:216944","phenotype":{"types":[{"id":"HP:0002170","label":"Intracranial hemorrhage"}]}},{"entity":"ClinVarVariant:181713","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:53915","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"dbSNP:rs42436295","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:12661","phenotype":{"types":[{"id":"HP:0008981","label":"Calf muscle hypertrophy"}]}},{"entity":"ClinVarVariant:11040","phenotype":{"types":[{"id":"HP:0007411","label":"Hypoplastic-absent sebaceous glands"}]}},{"entity":"ClinVarVariant:143171","phenotype":{"types":[{"id":"HP:0001123","label":"Visual field defect"}]}},{"entity":"ClinVarVariant:53990","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"ClinVarVariant:24866","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"FlyBase:FBal0296742","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007029-WBRNAi00088606","phenotype":{"types":[{"id":"WBPhenotype:0002057","label":"Bacillus thuringiensis toxin hypersensitive"}]}},{"entity":"ClinVarVariant:161357","phenotype":{"types":[{"id":"HP:0000303","label":"Mandibular prognathia"}]}},{"entity":"FlyBase:FBal0204265","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:65606","phenotype":{"types":[{"id":"HP:0001507","label":"Growth abnormality"}]}},{"entity":"ClinVarVariant:53961","phenotype":{"types":[{"id":"HP:0011947","label":"Respiratory tract infection"}]}},{"entity":"ClinVarVariant:135882","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:38742","phenotype":{"types":[{"id":"HP:0000519","label":"Congenital cataract"}]}},{"entity":"ClinVarVariant:41146","phenotype":{"types":[{"id":"HP:0100267","label":"Lip pit"}]}},{"entity":"ClinVarVariant:53803","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:189663","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:24409","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"MGI:2449695","phenotype":{"types":[{"id":"MP:0002563","label":"shortened circadian period"}]}},{"entity":"ClinVarVariant:24611","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:53964","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:189931","phenotype":{"types":[{"id":"HP:0005484","label":"Postnatal microcephaly"}]}},{"entity":"ClinVarVariant:30665","phenotype":{"types":[{"id":"HP:0000230","label":"Gingivitis"}]}},{"entity":"ClinVarVariant:40257","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"MGI:1856209","phenotype":{"types":[{"id":"GO:0021953PHENOTYPE","label":"central nervous system neuron differentiation phenotype"}]}},{"entity":"ClinVarVariant:24512","phenotype":{"types":[{"id":"HP:0000099","label":"Glomerulonephritis"}]}},{"entity":"ClinVarVariant:44811","phenotype":{"types":[{"id":"HP:0009891","label":"Underdeveloped supraorbital ridges"}]}},{"entity":"ClinVarVariant:8870","phenotype":{"types":[{"id":"HP:0002823","label":"Abnormality of the femur"}]}},{"entity":"ClinVarVariant:10156","phenotype":{"types":[{"id":"HP:0005268","label":"Spontaneous abortion"}]}},{"entity":"ClinVarVariant:210476","phenotype":{"types":[{"id":"HP:0003819","label":"Death in childhood"}]}},{"entity":"MGI:4818801","phenotype":{"types":[{"id":"HP:0001899","label":"Increased hematocrit"}]}},{"entity":"ClinVarVariant:10733","phenotype":{"types":[{"id":"HP:0009763","label":"Limb pain"}]}},{"entity":"FlyBase:FBal0102482","phenotype":{"types":[{"id":"FBcv:0000377","label":"female fertile"}]}},{"entity":"AQTL:54943","phenotype":{"types":[{"id":"AQTLTrait:1004","label":"Somatic cell count"}]}},{"entity":"ClinVarVariant:56625","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:6574","phenotype":{"types":[{"id":"HP:0010783","label":"Erythema"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004813-WBRNAi00075001","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:13823","phenotype":{"types":[{"id":"HP:0002164","label":"Nail dysplasia"}]}},{"entity":"ClinVarVariant:195148","phenotype":{"types":[{"id":"HP:0004327","label":"Abnormality of the vitreous humor"}]}},{"entity":"ClinVarVariant:40502","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:135886","phenotype":{"types":[{"id":"HP:0009733","label":"Glioma"}]}},{"entity":"ClinVarVariant:53932","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:49565","phenotype":{"types":[{"id":"HP:0009716","label":"Subependymal nodules"}]}},{"entity":"ClinVarVariant:13658","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"ClinVarVariant:21160","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"MGI:1857872","phenotype":{"types":[{"id":"MP:0008813","label":"decreased common myeloid progenitor cell number"}]}},{"entity":"ClinVarVariant:183748","phenotype":{"types":[{"id":"HP:0100568","label":"Neoplasm of the endocrine system"}]}},{"entity":"ClinVarVariant:50050","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"ClinVarVariant:56475","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:17974","phenotype":{"types":[{"id":"HP:0002613","label":"Biliary cirrhosis"}]}},{"entity":"MGI:1860866","phenotype":{"types":[{"id":"GO:0051209PHENOTYPE","label":"release of sequestered calcium ion into cytosol phenotype"}]}},{"entity":"MGI:3044898","phenotype":{"types":[{"id":"MP:0013716","label":"hypolactation"}]}},{"entity":"ClinVarVariant:216231","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:188863","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"ClinVarVariant:162395","phenotype":{"types":[{"id":"HP:0010819","label":"Atonic seizures"}]}},{"entity":"MGI:3027823","phenotype":{"types":[{"id":"MP:0001929","label":"abnormal gametogenesis"}]}},{"entity":"ClinVarVariant:1075","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"WormBase:WBVar00094804","phenotype":{"types":[{"id":"WBPhenotype:0001059","label":"magnesium chemotaxis defective"}]}},{"entity":"ClinVarVariant:13001","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:4849547","phenotype":{"types":[{"id":"HP:0002213","label":"Fine hair"}]}},{"entity":"ClinVarVariant:143564","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"ClinVarVariant:209010","phenotype":{"types":[{"id":"HP:0100660","label":"Dyskinesia"}]}},{"entity":"ClinVarVariant:210389","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"MGI:3848347","phenotype":{"types":[{"id":"GO:0008584PHENOTYPE","label":"male gonad development phenotype"}]}},{"entity":"ClinVarVariant:24268","phenotype":{"types":[{"id":"HP:0100273","label":"Neoplasm of the colon"}]}},{"entity":"ClinVarVariant:143744","phenotype":{"types":[{"id":"HP:0002120","label":"Cerebral cortical atrophy"}]}},{"entity":"ClinVarVariant:68490","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001337-WBRNAi00096891","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:132795","phenotype":{"types":[{"id":"HP:0001874","label":"Abnormality of neutrophils"}]}},{"entity":"ClinVarVariant:158349","phenotype":{"types":[{"id":"HP:0009765","label":"Low hanging columella"}]}},{"entity":"ClinVarVariant:65343","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:11642","phenotype":{"types":[{"id":"HP:0006887","label":"Intellectual disability, progressive"}]}},{"entity":"ClinVarVariant:161287","phenotype":{"types":[{"id":"HP:0001084","label":"Corneal arcus"}]}},{"entity":"ClinVarVariant:29790","phenotype":{"types":[{"id":"HP:0003690","label":"Limb muscle weakness"}]}},{"entity":"MGI:2682016","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"MGI:1932294","phenotype":{"types":[{"id":"HP:0012447","label":"Abnormal myelination"}]}},{"entity":"ClinVarVariant:6794","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:24762","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:21252","phenotype":{"types":[{"id":"HP:0000202","label":"Oral cleft"}]}},{"entity":"ClinVarVariant:53933","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:49411","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"MGI:2136432","phenotype":{"types":[{"id":"MP:0001284","label":"absent vibrissae"}]}},{"entity":"dbSNP:rs109445675","phenotype":{"types":[{"id":"AQTLTrait:1130","label":"Udder cleft"}]}},{"entity":"ClinVarVariant:10912","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"FlyBase:FBal0197136","phenotype":{"types":[{"id":"FBcv:0000397","label":"learning defective"}]}},{"entity":"ClinVarVariant:42756","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:36501","phenotype":{"types":[{"id":"HP:0002633","label":"Vasculitis"}]}},{"entity":"ClinVarVariant:101125","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"ClinVarVariant:6834","phenotype":{"types":[{"id":"HP:0000337","label":"Broad forehead"}]}},{"entity":"FlyBase:FBal0206542","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:9162","phenotype":{"types":[{"id":"HP:0011106","label":"Hypovolemia"}]}},{"entity":"ClinVarVariant:692","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:204026","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:1775","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:164883","phenotype":{"types":[{"id":"HP:0000540","label":"Hypermetropia"}]}},{"entity":"ClinVarVariant:10249","phenotype":{"types":[{"id":"HP:0100845","label":"Anaphylactic shock"}]}},{"entity":"ClinVarVariant:53724","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:24448","phenotype":{"types":[{"id":"HP:0200020","label":"Corneal erosion"}]}},{"entity":"ClinVarVariant:43146","phenotype":{"types":[{"id":"HP:0008555","label":"Absent vestibular function"}]}},{"entity":"ClinVarVariant:54021","phenotype":{"types":[{"id":"HP:0005948","label":"Cystic lung disease"}]}},{"entity":"ClinVarVariant:202199","phenotype":{"types":[{"id":"HP:0005257","label":"Thoracic hypoplasia"}]}},{"entity":"ClinVarVariant:24339","phenotype":{"types":[{"id":"HP:0100539","label":"Periorbital edema"}]}},{"entity":"ClinVarVariant:136155","phenotype":{"types":[{"id":"HP:0000582","label":"Upslanted palpebral fissure"}]}},{"entity":"ClinVarVariant:91600","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:50098","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"ZFIN:ZDB-ALT-071108-4","phenotype":{"types":[{"id":"ZP:0005125","label":"abnormal(ly) decreased size swim bladder"}]}},{"entity":"ClinVarVariant:1371","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"ClinVarVariant:56662","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:6540","phenotype":{"types":[{"id":"HP:0200042","label":"Skin ulcer"}]}},{"entity":"ClinVarVariant:210388","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"ClinVarVariant:40726","phenotype":{"types":[{"id":"HP:0000027","label":"Azoospermia"}]}},{"entity":"ClinVarVariant:24996","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:100739","phenotype":{"types":[{"id":"HP:0000484","label":"Hyperopic astigmatism"}]}},{"entity":"ClinVarVariant:189599","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"ClinVarVariant:158080","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:678","phenotype":{"types":[{"id":"HP:0005543","label":"Reduced protein C activity"}]}},{"entity":"ClinVarVariant:159036","phenotype":{"types":[{"id":"HP:0200054","label":"Monodactyly (feet)"}]}},{"entity":"ClinVarVariant:188984","phenotype":{"types":[{"id":"HP:0006887","label":"Intellectual disability, progressive"}]}},{"entity":"ClinVarVariant:6593","phenotype":{"types":[{"id":"HP:0003155","label":"Elevated alkaline phosphatase"}]}},{"entity":"ClinVarVariant:133628","phenotype":{"types":[{"id":"HP:0005425","label":"Recurrent sinopulmonary infections"}]}},{"entity":"ClinVarVariant:217297","phenotype":{"types":[{"id":"HP:0001144","label":"Orbital cyst"}]}},{"entity":"ClinVarVariant:40869","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004873-WBRNAi00037161","phenotype":{"types":[{"id":"WBPhenotype:0000025","label":"blistered"}]}},{"entity":"ClinVarVariant:41095","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:189125","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:6969","phenotype":{"types":[{"id":"HP:0003148","label":"Elevated serum acid phosphatase"}]}},{"entity":"ClinVarVariant:194120","phenotype":{"types":[{"id":"HP:0000657","label":"Oculomotor apraxia"}]}},{"entity":"ClinVarVariant:56314","phenotype":{"types":[{"id":"HP:0001562","label":"Oligohydramnios"}]}},{"entity":"MGI:2679338","phenotype":{"types":[{"id":"MP:0001473","label":"reduced long term potentiation"}]}},{"entity":"ClinVarVariant:56354","phenotype":{"types":[{"id":"HP:0012156","label":"Hemophagocytosis"}]}},{"entity":"ClinVarVariant:7152","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:210259","phenotype":{"types":[{"id":"HP:0002592","label":"Gastric ulcer"}]}},{"entity":"FlyBase:FBal0057699","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:10649","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:101259","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:157613","phenotype":{"types":[{"id":"HP:0000510","label":"Rod-cone dystrophy"}]}},{"entity":"ClinVarVariant:189653","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:210033","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:13343","phenotype":{"types":[{"id":"HP:0008357","label":"Reduced factor XIII activity"}]}},{"entity":"ClinVarVariant:40525","phenotype":{"types":[{"id":"HP:0030084","label":"Clinodactyly"}]}},{"entity":"ClinVarVariant:45358","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"ClinVarVariant:190395","phenotype":{"types":[{"id":"HP:0011100","label":"Intestinal atresia"}]}},{"entity":"MGI:2384087","phenotype":{"types":[{"id":"HP:0040171","label":"Decreased serum testosterone level"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008476-WBRNAi00024985","phenotype":{"types":[{"id":"WBPhenotype:0000054","label":"larval lethal"}]}},{"entity":"AQTL:30584","phenotype":{"types":[{"id":"AQTLTrait:1559","label":"Cell-mediated immune response"}]}},{"entity":"ClinVarVariant:204107","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:127339","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00018156-WBRNAi00087047","phenotype":{"types":[{"id":"WBPhenotype:0000038","label":"exploded through vulva"}]}},{"entity":"FlyBase:FBal0117671","phenotype":{"types":[{"id":"FBcv:0000358","label":"small body"}]}},{"entity":"MGI:1926498","phenotype":{"types":[{"id":"HP:0000962","label":"Hyperkeratosis"}]}},{"entity":"ClinVarVariant:52348","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"MGI:5297555","phenotype":{"types":[{"id":"MP:0001258","label":"decreased body length"}]}},{"entity":"AQTL:14959","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002226-WBRNAi00074011","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:17112","phenotype":{"types":[{"id":"HP:0007759","label":"Opacification of the corneal stroma"}]}},{"entity":"ClinVarVariant:7624","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:4566","phenotype":{"types":[{"id":"HP:0003487","label":"Babinski sign"}]}},{"entity":"ClinVarVariant:41167","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:132684","phenotype":{"types":[{"id":"HP:0000982","label":"Palmoplantar keratoderma"}]}},{"entity":"MGI:2183411","phenotype":{"types":[{"id":"HP:0011805","label":"Abnormality of muscle morphology"}]}},{"entity":"FlyBase:FBal0210631","phenotype":{"types":[{"id":"FBbt:00005179PHENOTYPE","label":"Drosophila macrochaeta phenotype"}]}},{"entity":"ClinVarVariant:11742","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:66001","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:97544","phenotype":{"types":[{"id":"HP:0000999","label":"Pyoderma"}]}},{"entity":"ClinVarVariant:3364","phenotype":{"types":[{"id":"HP:0001012","label":"Multiple lipomas"}]}},{"entity":"MGI:1857711","phenotype":{"types":[{"id":"GO:0007281PHENOTYPE","label":"germ cell development phenotype"}]}},{"entity":"ClinVarVariant:97000","phenotype":{"types":[{"id":"HP:0000012","label":"Urinary urgency"}]}},{"entity":"MGI:3762119","phenotype":{"types":[{"id":"HP:0011018","label":"Abnormality of the cell cycle"}]}},{"entity":"ClinVarVariant:682","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:159807","phenotype":{"types":[{"id":"HP:0000405","label":"Conductive hearing impairment"}]}},{"entity":"ClinVarVariant:16635","phenotype":{"types":[{"id":"HP:0002027","label":"Abdominal pain"}]}},{"entity":"ClinVarVariant:49482","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"ClinVarVariant:68721","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"dbSNP:rs41668337","phenotype":{"types":[{"id":"AQTLTrait:1115","label":"Chest width"}]}},{"entity":"FlyBase:FBal0239202","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:196726","phenotype":{"types":[{"id":"HP:0001030","label":"Fragile skin"}]}},{"entity":"ClinVarVariant:45344","phenotype":{"types":[{"id":"HP:0004808","label":"Acute myeloid leukemia"}]}},{"entity":"AQTL:3668","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:189693","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:53715","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"dbSNP:rs109089392","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"ClinVarVariant:49560","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:54195","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:204076","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:67917","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:5823","phenotype":{"types":[{"id":"HP:0008472","label":"Prominent protruding coccyx"}]}},{"entity":"ClinVarVariant:2656","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:17112","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"dbSNP:rs3800569","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:40522","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"MGI:1857826","phenotype":{"types":[{"id":"MP:0004453","label":"abnormal pterygoid bone morphology"}]}},{"entity":"ClinVarVariant:66473","phenotype":{"types":[{"id":"HP:0007360","label":"Aplasia/Hypoplasia of the cerebellum"}]}},{"entity":"ClinVarVariant:43580","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"MGI:2656537","phenotype":{"types":[{"id":"HP:0001322","label":"Brain very small"}]}},{"entity":"ClinVarVariant:49781","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:31562","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:39479","phenotype":{"types":[{"id":"HP:0000944","label":"Abnormality of the metaphyses"}]}},{"entity":"ClinVarVariant:188339","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:35840","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:39824","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:211909","phenotype":{"types":[{"id":"HP:0007772","label":"Impaired smooth pursuit"}]}},{"entity":"ClinVarVariant:1078","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:127707","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008053-WBRNAi00093392","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"MGI:3772332","phenotype":{"types":[{"id":"MP:0008209","label":"decreased pre-B cell number"}]}},{"entity":"ClinVarVariant:65877","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:31054","phenotype":{"types":[{"id":"HP:0000625","label":"Cleft eyelid"}]}},{"entity":"ClinVarVariant:18337","phenotype":{"types":[{"id":"HP:0009773","label":"Symphalangism affecting the phalanges of the hand"}]}},{"entity":"ClinVarVariant:53397","phenotype":{"types":[{"id":"HP:0005214","label":"Intestinal obstruction"}]}},{"entity":"WormBase:WBVar00089700","phenotype":{"types":[{"id":"WBPhenotype:0000216","label":"cell fate specification variant"}]}},{"entity":"MGI:5691529","phenotype":{"types":[{"id":"HP:0003196","label":"Short nose"}]}},{"entity":"FlyBase:FBal0117901","phenotype":{"types":[{"id":"FBbt:00001055PHENOTYPE","label":"presumptive embryonic/larval nervous system phenotype"}]}},{"entity":"ClinVarVariant:53754","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"MGI:4881474","phenotype":{"types":[{"id":"MP:0002945","label":"abnormal inhibitory postsynaptic currents"}]}},{"entity":"ClinVarVariant:42177","phenotype":{"types":[{"id":"HP:0002110","label":"Bronchiectasis"}]}},{"entity":"ClinVarVariant:101218","phenotype":{"types":[{"id":"HP:0100585","label":"Telangiectasia of the skin"}]}},{"entity":"ClinVarVariant:209131","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:7393","phenotype":{"types":[{"id":"HP:0000135","label":"Hypogonadism"}]}},{"entity":"ClinVarVariant:95639","phenotype":{"types":[{"id":"HP:0009909","label":"Uplifted earlobe"}]}},{"entity":"ClinVarVariant:49771","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:101223","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"ClinVarVariant:10053","phenotype":{"types":[{"id":"HP:0007325","label":"Generalized dystonia"}]}},{"entity":"ClinVarVariant:56402","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:3862","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"_:genid1975835","phenotype":{"types":[{"id":"ZP:0001663","label":"abnormal(ly) increased branchiness motor neuron axon"}]}},{"entity":"ClinVarVariant:24237","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"FlyBase:FBal0268981","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:166813","phenotype":{"types":[{"id":"HP:0010780","label":"Hyperacusis"}]}},{"entity":"ClinVarVariant:181733","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"MGI:3691651","phenotype":{"types":[{"id":"HP:0003330","label":"Abnormal bone structure"}]}},{"entity":"FlyBase:FBal0200319","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:215765","phenotype":{"types":[{"id":"HP:0005562","label":"Multiple renal cysts"}]}},{"entity":"FlyBase:FBal0190677","phenotype":{"types":[{"id":"FBbt:00005378PHENOTYPE","label":"wing margin phenotype"}]}},{"entity":"ClinVarVariant:53650","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:13329","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:54009","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"MGI:5297120","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:7184","phenotype":{"types":[{"id":"HP:0100027","label":"Recurrent pancreatitis"}]}},{"entity":"ClinVarVariant:49286","phenotype":{"types":[{"id":"HP:0009717","label":"Cortical tubers"}]}},{"entity":"ClinVarVariant:101289","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:11707","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:99920","phenotype":{"types":[{"id":"HP:0000289","label":"Broad philtrum"}]}},{"entity":"ClinVarVariant:17229","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1756","phenotype":{"types":[{"id":"ZP:0000212","label":"abnormal(ly) viability whole organism"}]}},{"entity":"ClinVarVariant:156620","phenotype":{"types":[{"id":"HP:0100021","label":"Cerebral palsy"}]}},{"entity":"ClinVarVariant:54067","phenotype":{"types":[{"id":"HP:0011109","label":"Chronic sinusitis"}]}},{"entity":"ClinVarVariant:53736","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"MGI:2179460","phenotype":{"types":[{"id":"MP:0009678","label":"abnormal spinal cord lateral column morphology"}]}},{"entity":"ClinVarVariant:188794","phenotype":{"types":[{"id":"HP:0002015","label":"Dysphagia"}]}},{"entity":"ClinVarVariant:12000","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00020263-WBRNAi00026196","phenotype":{"types":[{"id":"WBPhenotype:0000697","label":"protruding vulva"}]}},{"entity":"ClinVarVariant:68596","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:210780","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:41258","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"ClinVarVariant:4627","phenotype":{"types":[{"id":"HP:0003390","label":"Sensory axonal neuropathy"}]}},{"entity":"ClinVarVariant:21156","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ZFIN:ZDB-ALT-080325-1","phenotype":{"types":[{"id":"ZP:0015389","label":"abnormal(ly) non-functional sperm mitochondrion"}]}},{"entity":"ClinVarVariant:159236","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:30170","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:12672","phenotype":{"types":[{"id":"HP:0000963","label":"Thin skin"}]}},{"entity":"ClinVarVariant:9001","phenotype":{"types":[{"id":"HP:0010971","label":"Absence of Lutheran antigen on erythrocytes"}]}},{"entity":"ClinVarVariant:210789","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"MGI:3576671","phenotype":{"types":[{"id":"HP:0000021","label":"Megacystis"}]}},{"entity":"ClinVarVariant:10758","phenotype":{"types":[{"id":"HP:0000763","label":"Sensory neuropathy"}]}},{"entity":"ClinVarVariant:10063","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:53952","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050913-84-ZDB-MRPHLNO-070713-2","phenotype":{"types":[{"id":"ZP:0007928","label":"abnormal(ly) edematous heart sarcolemma"}]}},{"entity":"ClinVarVariant:66925","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"MGI:2150346","phenotype":{"types":[{"id":"MP:0009039","label":"absent inferior colliculus"}]}},{"entity":"ClinVarVariant:12607","phenotype":{"types":[{"id":"HP:0000474","label":"Thickened nuchal skin fold"}]}},{"entity":"FlyBase:FBal0230895","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:36132","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:180361","phenotype":{"types":[{"id":"HP:0011645","label":"Sinus of Valsalva aneurysm"}]}},{"entity":"ClinVarVariant:11010","phenotype":{"types":[{"id":"HP:0002021","label":"Pyloric stenosis"}]}},{"entity":"ClinVarVariant:9378","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:65730","phenotype":{"types":[{"id":"HP:0000722","label":"Obsessive-compulsive behavior"}]}},{"entity":"MGI:3036704","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"ClinVarVariant:14087","phenotype":{"types":[{"id":"HP:0001712","label":"Left ventricular hypertrophy"}]}},{"entity":"FlyBase:FBal0204597","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:16911","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:53117","phenotype":{"types":[{"id":"HP:0006696","label":"Polymorphic and polytopic ventricular extrasystoles"}]}},{"entity":"ClinVarVariant:56312","phenotype":{"types":[{"id":"HP:0002323","label":"Anencephaly"}]}},{"entity":"ClinVarVariant:24391","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"ClinVarVariant:94001","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:10289","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:6207","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:127348","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"FlyBase:FBal0202458","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:180411","phenotype":{"types":[{"id":"HP:0100749","label":"Chest pain"}]}},{"entity":"ClinVarVariant:200598","phenotype":{"types":[{"id":"HP:0006696","label":"Polymorphic and polytopic ventricular extrasystoles"}]}},{"entity":"ClinVarVariant:53214","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:11819","phenotype":{"types":[{"id":"HP:0000721","label":"Lack of spontaneous play"}]}},{"entity":"AQTL:51680","phenotype":{"types":[{"id":"AQTLTrait:1120","label":"Thurl width"}]}},{"entity":"FlyBase:FBal0124348","phenotype":{"types":[{"id":"FBcv:0000432","label":"mitotic cell cycle defective"}]}},{"entity":"ClinVarVariant:5086","phenotype":{"types":[{"id":"HP:0000666","label":"Horizontal nystagmus"}]}},{"entity":"dbSNP:rs16879552","phenotype":{"types":[{"id":"HP:0005249","label":"Functional intestinal obstruction"}]}},{"entity":"ClinVarVariant:101196","phenotype":{"types":[{"id":"HP:0000387","label":"Absent earlobe"}]}},{"entity":"MGI:4318693","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006366-WBRNAi00086348","phenotype":{"types":[{"id":"WBPhenotype:0000154","label":"reduced brood size"}]}},{"entity":"WormBase:WBVar00143937","phenotype":{"types":[{"id":"WBPhenotype:0000502","label":"right handed roller"}]}},{"entity":"ClinVarVariant:93356","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:55952","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:155982","phenotype":{"types":[{"id":"HP:0200085","label":"Limb tremor"}]}},{"entity":"ClinVarVariant:204102","phenotype":{"types":[{"id":"HP:0000121","label":"Nephrocalcinosis"}]}},{"entity":"MGI:3837125","phenotype":{"types":[{"id":"MP:0005154","label":"increased B cell proliferation"}]}},{"entity":"ClinVarVariant:36122","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:189043","phenotype":{"types":[{"id":"HP:0002967","label":"Cubitus valgus"}]}},{"entity":"ClinVarVariant:167563","phenotype":{"types":[{"id":"HP:0007018","label":"Attention deficit hyperactivity disorder"}]}},{"entity":"ClinVarVariant:216025","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:5973","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"MGI:2156086","phenotype":{"types":[{"id":"MP:0003645","label":"increased pancreatic beta cell number"}]}},{"entity":"ClinVarVariant:25340","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:216143","phenotype":{"types":[{"id":"HP:0001350","label":"Slurred speech"}]}},{"entity":"AQTL:49968","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"MGI:4440831","phenotype":{"types":[{"id":"MP:0011095","label":"embryonic lethality between implantation and placentation, complete penetrance"}]}},{"entity":"WormBase:WBVar00146423","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:7460","phenotype":{"types":[{"id":"HP:0000069","label":"Abnormality of the ureter"}]}},{"entity":"ClinVarVariant:157618","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"ClinVarVariant:10198","phenotype":{"types":[{"id":"HP:0100310","label":"Epidural hemorrhage"}]}},{"entity":"ClinVarVariant:53412","phenotype":{"types":[{"id":"HP:0001948","label":"Alkalosis"}]}},{"entity":"ClinVarVariant:189740","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:12016","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"MGI:4839231","phenotype":{"types":[{"id":"MP:0009977","label":"abnormal cerebellar granule cell migration"}]}},{"entity":"ClinVarVariant:50019","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:829","phenotype":{"types":[{"id":"HP:0000706","label":"Unerupted tooth"}]}},{"entity":"ClinVarVariant:66105","phenotype":{"types":[{"id":"HP:0001742","label":"Nasal obstruction"}]}},{"entity":"ClinVarVariant:10148","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"MGI:3510641","phenotype":{"types":[{"id":"MP:0003081","label":"abnormal soleus morphology"}]}},{"entity":"FlyBase:FBal0190270","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:204066","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:53902","phenotype":{"types":[{"id":"HP:0001082","label":"Cholecystitis"}]}},{"entity":"ClinVarVariant:18427","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00013144-WBRNAi00082701","phenotype":{"types":[{"id":"MP:0002209","label":"decreased germ cell number"}]}},{"entity":"ClinVarVariant:35733","phenotype":{"types":[{"id":"HP:0000934","label":"Chondrocalcinosis"}]}},{"entity":"ClinVarVariant:82630","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:11379","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:56465","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:48762","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:25036","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"ClinVarVariant:24670","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:162009","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:24292","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:189710","phenotype":{"types":[{"id":"HP:0000478","label":"Abnormality of the eye"}]}},{"entity":"AQTL:25469","phenotype":{"types":[{"id":"AQTLTrait:1044","label":"Milk yield"}]}},{"entity":"ClinVarVariant:24488","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:24581","phenotype":{"types":[{"id":"HP:0100586","label":"Aseptic leukocyturia"}]}},{"entity":"ClinVarVariant:183145","phenotype":{"types":[{"id":"HP:0010318","label":"Aplasia/Hypoplasia of the abdominal wall musculature"}]}},{"entity":"ClinVarVariant:49761","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:41939","phenotype":{"types":[{"id":"HP:0003741","label":"Congenital muscular dystrophy"}]}},{"entity":"ClinVarVariant:126837","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001929-WBRNAi00026532","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:97695","phenotype":{"types":[{"id":"HP:0100537","label":"Fasciitis"}]}},{"entity":"ClinVarVariant:139033","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:53744","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:9990","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"MGI:3811233","phenotype":{"types":[{"id":"MP:0000060","label":"delayed bone ossification"}]}},{"entity":"ClinVarVariant:92205","phenotype":{"types":[{"id":"HP:0000131","label":"Uterine leiomyoma"}]}},{"entity":"ClinVarVariant:53973","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:35456","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:55938","phenotype":{"types":[{"id":"HP:0006887","label":"Intellectual disability, progressive"}]}},{"entity":"ClinVarVariant:189683","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:143543","phenotype":{"types":[{"id":"HP:0010521","label":"Gait apraxia"}]}},{"entity":"ClinVarVariant:210299","phenotype":{"types":[{"id":"HP:0002592","label":"Gastric ulcer"}]}},{"entity":"ClinVarVariant:36794","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"ClinVarVariant:217164","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"AQTL:31966","phenotype":{"types":[{"id":"AQTLTrait:2161","label":"Femur length"}]}},{"entity":"ClinVarVariant:53219","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"ClinVarVariant:13325","phenotype":{"types":[{"id":"HP:0001644","label":"Dilated cardiomyopathy"}]}},{"entity":"ClinVarVariant:208080","phenotype":{"types":[{"id":"HP:0005478","label":"Prominent frontal sinuses"}]}},{"entity":"ClinVarVariant:42420","phenotype":{"types":[{"id":"HP:0000646","label":"Amblyopia"}]}},{"entity":"ClinVarVariant:35832","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"ClinVarVariant:36764","phenotype":{"types":[{"id":"HP:0006682","label":"Ventricular extrasystoles"}]}},{"entity":"ClinVarVariant:53493","phenotype":{"types":[{"id":"HP:0011109","label":"Chronic sinusitis"}]}},{"entity":"MGI:3590264","phenotype":{"types":[{"id":"MP:0001987","label":"alcohol preference"}]}},{"entity":"ClinVarVariant:6213","phenotype":{"types":[{"id":"HP:0003218","label":"Oroticaciduria"}]}},{"entity":"ClinVarVariant:53158","phenotype":{"types":[{"id":"HP:0004395","label":"Malnutrition"}]}},{"entity":"ClinVarVariant:188948","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00014883-WBRNAi00077884","phenotype":{"types":[{"id":"WBPhenotype:0001824","label":"meiotic progression prophase variant"}]}},{"entity":"ClinVarVariant:183330","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:41088","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:66501","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"MGI:2135666","phenotype":{"types":[{"id":"MP:0000166","label":"abnormal chondrocyte morphology"}]}},{"entity":"ClinVarVariant:2608","phenotype":{"types":[{"id":"HP:0011096","label":"Peripheral demyelination"}]}},{"entity":"ClinVarVariant:45017","phenotype":{"types":[{"id":"HP:0011663","label":"Right ventricular cardiomyopathy"}]}},{"entity":"ClinVarVariant:217252","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:6021","phenotype":{"types":[{"id":"HP:0002230","label":"Generalized hirsutism"}]}},{"entity":"ClinVarVariant:11755","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"MGI:2388715","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"MGI:4888719","phenotype":{"types":[{"id":"MP:0006060","label":"increased cerebral infarction size"}]}},{"entity":"ClinVarVariant:49751","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:162613","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:92705","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00016493-WBRNAi00096905","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"ClinVarVariant:36112","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:36577","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"FlyBase:FBal0209323","phenotype":{"types":[{"id":"FBcv:0000352","label":"partially lethal - majority die"}]}},{"entity":"ClinVarVariant:13162","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:25340","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:5509","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003084-WBRNAi00078913","phenotype":{"types":[{"id":"WBPhenotype:0000700","label":"multivulva"}]}},{"entity":"ClinVarVariant:211736","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"MGI:3775648","phenotype":{"types":[{"id":"HP:0012465","label":"Elevated hepatic iron concentration"}]}},{"entity":"ClinVarVariant:65274","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:11811","phenotype":{"types":[{"id":"HP:0000248","label":"Brachycephaly"}]}},{"entity":"ClinVarVariant:49741","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:158612","phenotype":{"types":[{"id":"HP:0007266","label":"Cerebral dysmyelination"}]}},{"entity":"MGI:2181021","phenotype":{"types":[{"id":"MP:0011086","label":"postnatal lethality, incomplete penetrance"}]}},{"entity":"MGI:4362924","phenotype":{"types":[{"id":"HP:0010976","label":"B lymphocytopenia"}]}},{"entity":"ClinVarVariant:2017","phenotype":{"types":[{"id":"HP:0000230","label":"Gingivitis"}]}},{"entity":"ClinVarVariant:2945","phenotype":{"types":[{"id":"HP:0000662","label":"Nyctalopia"}]}},{"entity":"ClinVarVariant:42325","phenotype":{"types":[{"id":"HP:0004933","label":"Ascending aortic dissection"}]}},{"entity":"WormBase:WBVar00252220","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:1451","phenotype":{"types":[{"id":"HP:0006597","label":"Diaphragmatic paralysis"}]}},{"entity":"ClinVarVariant:11082","phenotype":{"types":[{"id":"HP:0002361","label":"Psychomotor deterioration"}]}},{"entity":"ClinVarVariant:7192","phenotype":{"types":[{"id":"HP:0002608","label":"Celiac disease"}]}},{"entity":"ClinVarVariant:5280","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:36102","phenotype":{"types":[{"id":"HP:0002987","label":"Elbow flexion contracture"}]}},{"entity":"ClinVarVariant:2250","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"ClinVarVariant:101138","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"ClinVarVariant:10253","phenotype":{"types":[{"id":"HP:0005681","label":"Juvenile rheumatoid arthritis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00009882-WBRNAi00085534","phenotype":{"types":[{"id":"WBPhenotype:0001810","label":"oocyte septum formation variant"}]}},{"entity":"FlyBase:FBal0302452","phenotype":{"types":[{"id":"FBcv:0000316","label":"homeotic"}]}},{"entity":"ClinVarVariant:6810","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000962-WBRNAi00085605","phenotype":{"types":[{"id":"WBPhenotype:0001028","label":"nuclear appearance variant"}]}},{"entity":"ClinVarVariant:137950","phenotype":{"types":[{"id":"HP:0009765","label":"Low hanging columella"}]}},{"entity":"ClinVarVariant:53851","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:3670","phenotype":{"types":[{"id":"HP:0007957","label":"Corneal opacity"}]}},{"entity":"ClinVarVariant:143152","phenotype":{"types":[{"id":"HP:0002251","label":"Aganglionic megacolon"}]}},{"entity":"ClinVarVariant:162134","phenotype":{"types":[{"id":"HP:0007754","label":"Macular dystrophy"}]}},{"entity":"ClinVarVariant:211254","phenotype":{"types":[{"id":"HP:0001973","label":"Autoimmune thrombocytopenia"}]}},{"entity":"ClinVarVariant:167491","phenotype":{"types":[{"id":"HP:0002089","label":"Pulmonary hypoplasia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006928-WBRNAi00095274","phenotype":{"types":[{"id":"WBPhenotype:0001013","label":"pathogen susceptibility increased"}]}},{"entity":"ClinVarVariant:40678","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:42545","phenotype":{"types":[{"id":"HP:0000859","label":"Hyperaldosteronism"}]}},{"entity":"ClinVarVariant:180643","phenotype":{"types":[{"id":"HP:0002359","label":"Frequent falls"}]}},{"entity":"ClinVarVariant:65302","phenotype":{"types":[{"id":"HP:0000826","label":"Precocious puberty"}]}},{"entity":"ClinVarVariant:48947","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:4182","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:52338","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:41162","phenotype":{"types":[{"id":"HP:0003162","label":"Fasting hypoglycemia"}]}},{"entity":"MGI:2177337","phenotype":{"types":[{"id":"MP:0003934","label":"abnormal pancreas development"}]}},{"entity":"ClinVarVariant:2033","phenotype":{"types":[{"id":"HP:0000830","label":"Anterior hypopituitarism"}]}},{"entity":"ClinVarVariant:21244","phenotype":{"types":[{"id":"HP:0011362","label":"Abnormal hair quantity"}]}},{"entity":"MGI:2155977","phenotype":{"types":[{"id":"GO:0043066PHENOTYPE","label":"negative regulation of apoptotic process phenotype"}]}},{"entity":"ClinVarVariant:13903","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:184187","phenotype":{"types":[{"id":"HP:0005523","label":"Lymphoproliferative disorder"}]}},{"entity":"ClinVarVariant:126446","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:181723","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:3160","phenotype":{"types":[{"id":"HP:0001254","label":"Lethargy"}]}},{"entity":"ClinVarVariant:204097","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:10108","phenotype":{"types":[{"id":"HP:0005542","label":"Prolonged whole-blood clotting time"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000376-WBRNAi00027553","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"FlyBase:FBal0203410","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:49731","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:11736","phenotype":{"types":[{"id":"HP:0010808","label":"Protruding tongue"}]}},{"entity":"dbSNP:rs9268905","phenotype":{"types":[{"id":"HP:0002331","label":"Headache (with pheochromocytoma)"}]}},{"entity":"MGI:5548388","phenotype":{"types":[{"id":"HP:0005736","label":"Short tibia"}]}},{"entity":"WormBase:WBVar00242226","phenotype":{"types":[{"id":"WBPhenotype:0000470","label":"HSN migration variant"}]}},{"entity":"FlyBase:FBal0207110","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:41191","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:38985","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:204056","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:56302","phenotype":{"types":[{"id":"HP:0002323","label":"Anencephaly"}]}},{"entity":"ClinVarVariant:101279","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:196934","phenotype":{"types":[{"id":"HP:0002512","label":"Brain stem compression"}]}},{"entity":"MGI:2653045","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:4888","phenotype":{"types":[{"id":"HP:0100639","label":"Erectile abnormalities"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-990415-279-ZDB-MRPHLNO-070116-1","phenotype":{"types":[{"id":"GO:0021854PHENOTYPE","label":"hypothalamus development phenotype"}]}},{"entity":"ClinVarVariant:21595","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:41158","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"AQTL:15956","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:101279","phenotype":{"types":[{"id":"HP:0000015","label":"Bladder diverticulum"}]}},{"entity":"ClinVarVariant:13396","phenotype":{"types":[{"id":"HP:0007772","label":"Impaired smooth pursuit"}]}},{"entity":"ClinVarVariant:143704","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:5634328","phenotype":{"types":[{"id":"HP:0011970","label":"Cerebral amyloid angiopathy"}]}},{"entity":"AQTL:18099","phenotype":{"types":[{"id":"AQTLTrait:1153","label":"Stillbirth"}]}},{"entity":"ClinVarVariant:216145","phenotype":{"types":[{"id":"HP:0009806","label":"Nephrogenic diabetes insipidus"}]}},{"entity":"ClinVarVariant:53643","phenotype":{"types":[{"id":"HP:0100732","label":"Pancreatic fibrosis"}]}},{"entity":"ClinVarVariant:217069","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:1955","phenotype":{"types":[{"id":"HP:0001890","label":"Autoimmune hemolytic anemia"}]}},{"entity":"ClinVarVariant:39667","phenotype":{"types":[{"id":"HP:0006380","label":"Knee flexion contracture"}]}},{"entity":"AQTL:13689","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:209143","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:8762","phenotype":{"types":[{"id":"HP:0000988","label":"Skin rash"}]}},{"entity":"ZFIN:ZDB-ALT-050913-4","phenotype":{"types":[{"id":"ZP:0010859","label":"abnormal(ly) lacks parts or has fewer parts of type olfactory epithelium towards olfactory epithelium microvillous olfactory receptor neuron"}]}},{"entity":"ClinVarVariant:1221","phenotype":{"types":[{"id":"HP:0002063","label":"Rigidity"}]}},{"entity":"FlyBase:FBal0199572","phenotype":{"types":[{"id":"FBbt:00005169PHENOTYPE","label":"Drosophila trichogen cell phenotype"}]}},{"entity":"ClinVarVariant:7161","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"MGI:1931048","phenotype":{"types":[{"id":"GO:0001525PHENOTYPE","label":"angiogenesis phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001686-WBRNAi00023783","phenotype":{"types":[{"id":"WBPhenotype:0001183","label":"fat content reduced"}]}},{"entity":"ClinVarVariant:49805","phenotype":{"types":[{"id":"HP:0009720","label":"Adenoma sebaceum"}]}},{"entity":"ClinVarVariant:50874","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:53942","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"AQTL:20964","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"ClinVarVariant:183242","phenotype":{"types":[{"id":"HP:0003687","label":"Centrally nucleated skeletal muscle fibers"}]}},{"entity":"ClinVarVariant:21057","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:49848","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"MGI:4367072","phenotype":{"types":[{"id":"MP:0004753","label":"abnormal miniature excitatory postsynaptic currents"}]}},{"entity":"FlyBase:FBal0292824","phenotype":{"types":[{"id":"FBcv:0000366","label":"female sterile"}]}},{"entity":"FlyBase:FBal0130285","phenotype":{"types":[{"id":"FBcv:0000449","label":"planar polarity defective"}]}},{"entity":"ClinVarVariant:38887","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-001212-6-ZDB-MRPHLNO-060215-2","phenotype":{"types":[{"id":"ZP:0000955","label":"abnormal(ly) disrupted determination of heart left/right asymmetry"}]}},{"entity":"MGI:3528994","phenotype":{"types":[{"id":"MP:0005463","label":"abnormal CD4-positive, alpha-beta T cell physiology"}]}},{"entity":"ClinVarVariant:68698","phenotype":{"types":[{"id":"HP:0002900","label":"Hypokalemia"}]}},{"entity":"ClinVarVariant:53390","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:216707","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"ClinVarVariant:56027","phenotype":{"types":[{"id":"HP:0008434","label":"Hypoplastic cervical vertebrae"}]}},{"entity":"ClinVarVariant:126651","phenotype":{"types":[{"id":"HP:0000864","label":"Abnormality of the hypothalamus-pituitary axis"}]}},{"entity":"ClinVarVariant:82337","phenotype":{"types":[{"id":"HP:0006753","label":"Neoplasm of the stomach"}]}},{"entity":"dbSNP:rs29015207","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:4881","phenotype":{"types":[{"id":"HP:0000771","label":"Gynecomastia"}]}},{"entity":"ClinVarVariant:156326","phenotype":{"types":[{"id":"HP:0001762","label":"Talipes equinovarus"}]}},{"entity":"ClinVarVariant:3211","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007385-WBRNAi00028603","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"ClinVarVariant:92521","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"ClinVarVariant:10756","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"ClinVarVariant:11000","phenotype":{"types":[{"id":"HP:0002021","label":"Pyloric stenosis"}]}},{"entity":"MGI:3698867","phenotype":{"types":[{"id":"MP:0002047","label":"increased hepatic hemangioma incidence"}]}},{"entity":"ClinVarVariant:53648","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:53396","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:126952","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:135756","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:10194","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:204268","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:1641","phenotype":{"types":[{"id":"HP:0002942","label":"Thoracic kyphosis"}]}},{"entity":"WormBase:WBVar00089870","phenotype":{"types":[{"id":"WBPhenotype:0000425","label":"antibody staining reduced"}]}},{"entity":"ClinVarVariant:135702","phenotype":{"types":[{"id":"HP:0000684","label":"Delayed eruption of teeth"}]}},{"entity":"MGI:2137553","phenotype":{"types":[{"id":"MP:0001698","label":"decreased embryo size"}]}},{"entity":"MGI:1933761","phenotype":{"types":[{"id":"HP:0100522","label":"Thymoma"}]}},{"entity":"ClinVarVariant:135767","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:1391","phenotype":{"types":[{"id":"HP:0004639","label":"Elevated amniotic fluid alpha-fetoprotein"}]}},{"entity":"ClinVarVariant:49307","phenotype":{"types":[{"id":"HP:0009554","label":"Projection of scalp hair onto lateral cheek"}]}},{"entity":"MGI:5629408","phenotype":{"types":[{"id":"HP:0003097","label":"Short femur"}]}},{"entity":"ClinVarVariant:18334","phenotype":{"types":[{"id":"HP:0007110","label":"Central hypoventilation"}]}},{"entity":"_:genid1976156","phenotype":{"types":[{"id":"ZP:0000038","label":"abnormal(ly) edematous pericardium"}]}},{"entity":"ClinVarVariant:24775","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:9450","phenotype":{"types":[{"id":"HP:0000455","label":"Broad nasal tip"}]}},{"entity":"ClinVarVariant:204096","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:2764","phenotype":{"types":[{"id":"HP:0003019","label":"Abnormality of the wrist"}]}},{"entity":"ClinVarVariant:16814","phenotype":{"types":[{"id":"HP:0011663","label":"Right ventricular cardiomyopathy"}]}},{"entity":"ClinVarVariant:29667","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"ClinVarVariant:16303","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:181735","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:161992","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"ClinVarVariant:17272","phenotype":{"types":[{"id":"HP:0004277","label":"Fractured hand bones"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002202-WBRNAi00101493","phenotype":{"types":[{"id":"WBPhenotype:0001887","label":"excess seam cells"}]}},{"entity":"ClinVarVariant:13898","phenotype":{"types":[{"id":"HP:0001558","label":"Decreased fetal movement"}]}},{"entity":"ClinVarVariant:49526","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:24694","phenotype":{"types":[{"id":"HP:0011502","label":"Posterior lenticonus"}]}},{"entity":"FlyBase:FBal0204414","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:40983","phenotype":{"types":[{"id":"HP:0002757","label":"Recurrent fractures"}]}},{"entity":"ClinVarVariant:102723","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:14700","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:54043","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:55824","phenotype":{"types":[{"id":"HP:0001900","label":"Increased hemoglobin"}]}},{"entity":"ClinVarVariant:160314","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:159229","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:8882","phenotype":{"types":[{"id":"HP:0006989","label":"Dysplastic corpus callosum"}]}},{"entity":"ClinVarVariant:3167","phenotype":{"types":[{"id":"HP:0003419","label":"Low back pain"}]}},{"entity":"MGI:2152978","phenotype":{"types":[{"id":"HP:0008873","label":"Disproportionate short-limb short stature"}]}},{"entity":"ClinVarVariant:12975","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:127425","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:7519","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:54073","phenotype":{"types":[{"id":"HP:0006536","label":"Obstructive lung disease"}]}},{"entity":"ClinVarVariant:163768","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ZFIN:ZDB-ALT-980203-483","phenotype":{"types":[{"id":"ZP:0001317","label":"abnormal(ly) condensed pharyngeal arch cartilage"}]}},{"entity":"ClinVarVariant:192382","phenotype":{"types":[{"id":"HP:0000303","label":"Mandibular prognathia"}]}},{"entity":"ClinVarVariant:120303","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:157598","phenotype":{"types":[{"id":"HP:0001231","label":"Abnormality of the fingernails"}]}},{"entity":"MGI:3620559","phenotype":{"types":[{"id":"MP:0003719","label":"abnormal pericyte morphology"}]}},{"entity":"ClinVarVariant:216935","phenotype":{"types":[{"id":"HP:0000900","label":"Thickened ribs"}]}},{"entity":"ClinVarVariant:24548","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:143491","phenotype":{"types":[{"id":"HP:0010521","label":"Gait apraxia"}]}},{"entity":"MGI:3797077","phenotype":{"types":[{"id":"MP:0013283","label":"failure of ventral body wall closure"}]}},{"entity":"ClinVarVariant:8814","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:140832","phenotype":{"types":[{"id":"HP:0002344","label":"Progressive neurologic deterioration"}]}},{"entity":"MGI:2180365","phenotype":{"types":[{"id":"MP:0000097","label":"short maxilla"}]}},{"entity":"ClinVarVariant:56455","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:94811","phenotype":{"types":[{"id":"HP:0003713","label":"Muscle fiber necrosis"}]}},{"entity":"MGI:3579497","phenotype":{"types":[{"id":"MP:0001728","label":"failure of embryo implantation"}]}},{"entity":"ClinVarVariant:36113","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:7185","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"FlyBase:FBal0244010","phenotype":{"types":[{"id":"FBbt:00004283PHENOTYPE","label":"Drosophila prothoracic tarsal bristle phenotype"}]}},{"entity":"ClinVarVariant:101145","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:7444","phenotype":{"types":[{"id":"HP:0000771","label":"Gynecomastia"}]}},{"entity":"MGI:4457504","phenotype":{"types":[{"id":"HP:0003076","label":"Glycosuria"}]}},{"entity":"ClinVarVariant:50854","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"MGI:2449290","phenotype":{"types":[{"id":"HP:0100738","label":"Abnormal eating behavior"}]}},{"entity":"ClinVarVariant:5859","phenotype":{"types":[{"id":"HP:0000684","label":"Delayed eruption of teeth"}]}},{"entity":"ClinVarVariant:41151","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:1985","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:66441","phenotype":{"types":[{"id":"HP:0100707","label":"Abnormality of the astrocytes"}]}},{"entity":"MGI:2386172","phenotype":{"types":[{"id":"MP:0002118","label":"abnormal lipid homeostasis"}]}},{"entity":"ClinVarVariant:53972","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:42363","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"MGI:2150350","phenotype":{"types":[{"id":"HP:0001669","label":"Transposition of the great arteries"}]}},{"entity":"ClinVarVariant:127150","phenotype":{"types":[{"id":"HP:0001321","label":"Cerebellar hypoplasia"}]}},{"entity":"MGI:1855936","phenotype":{"types":[{"id":"HP:0009887","label":"Abnormality of hair pigmentation"}]}},{"entity":"_:genid1972365","phenotype":{"types":[{"id":"ZP:0014893","label":"abnormal(ly) process quality response to gamma radiation"}]}},{"entity":"ClinVarVariant:30547","phenotype":{"types":[{"id":"HP:0000972","label":"Palmoplantar hyperkeratosis"}]}},{"entity":"ClinVarVariant:53788","phenotype":{"types":[{"id":"HP:0100646","label":"Thyroiditis"}]}},{"entity":"MGI:3041864","phenotype":{"types":[{"id":"MP:0008395","label":"abnormal osteoblast differentiation"}]}},{"entity":"MGI:1856910","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:142043","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:216224","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:210843","phenotype":{"types":[{"id":"HP:0100495","label":"Mastocytosis"}]}},{"entity":"ClinVarVariant:25184","phenotype":{"types":[{"id":"HP:0004372","label":"Reduced consciousness/confusion"}]}},{"entity":"ClinVarVariant:143181","phenotype":{"types":[{"id":"HP:0001123","label":"Visual field defect"}]}},{"entity":"FlyBase:FBal0198615","phenotype":{"types":[{"id":"FBcv:0000386","label":"long lived"}]}},{"entity":"ClinVarVariant:189163","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:41364","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:7945","phenotype":{"types":[{"id":"HP:0000077","label":"Abnormality of the kidney"}]}},{"entity":"MGI:3051523","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"FlyBase:FBal0213272","phenotype":{"types":[{"id":"FBcv:0000356","label":"body color defective"}]}},{"entity":"ClinVarVariant:9143","phenotype":{"types":[{"id":"HP:0003455","label":"Elevated long chain fatty acids"}]}},{"entity":"ClinVarVariant:35823","phenotype":{"types":[{"id":"HP:0001742","label":"Nasal obstruction"}]}},{"entity":"ClinVarVariant:10460","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:101300","phenotype":{"types":[{"id":"HP:0100784","label":"Peripheral arteriovenous fistula"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022281-WBRNAi00098373","phenotype":{"types":[{"id":"WBPhenotype:0001566","label":"ventral enclosure variant"}]}},{"entity":"AQTL:28586","phenotype":{"types":[{"id":"AQTLTrait:1169","label":"Interval to first estrus after calving"}]}},{"entity":"dbSNP:rs43697015","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:10723","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"AQTL:13101","phenotype":{"types":[{"id":"AQTLTrait:1110","label":"Muscle protein percentage"}]}},{"entity":"ClinVarVariant:53234","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:17380","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:133325","phenotype":{"types":[{"id":"HP:0002317","label":"Unsteady gait"}]}},{"entity":"ClinVarVariant:93761","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"MGI:5320677","phenotype":{"types":[{"id":"HP:0001899","label":"Increased hematocrit"}]}},{"entity":"ClinVarVariant:159128","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:49173","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:36035","phenotype":{"types":[{"id":"HP:0000541","label":"Retinal detachment"}]}},{"entity":"ClinVarVariant:209052","phenotype":{"types":[{"id":"HP:0002107","label":"Pneumothorax"}]}},{"entity":"ClinVarVariant:204278","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:13560","phenotype":{"types":[{"id":"HP:0001873","label":"Thrombocytopenia"}]}},{"entity":"ClinVarVariant:2456","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"MGI:5548068","phenotype":{"types":[{"id":"MP:0001265","label":"decreased body size"}]}},{"entity":"ClinVarVariant:834","phenotype":{"types":[{"id":"HP:0006000","label":"Ureteral obstruction"}]}},{"entity":"ClinVarVariant:1676","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"FlyBase:FBal0125280","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"dbSNP:rs41628993","phenotype":{"types":[{"id":"AQTLTrait:1067","label":"Length of productive life"}]}},{"entity":"ClinVarVariant:3445","phenotype":{"types":[{"id":"HP:0000085","label":"Horseshoe kidney"}]}},{"entity":"ClinVarVariant:101410","phenotype":{"types":[{"id":"HP:0000790","label":"Hematuria"}]}},{"entity":"ClinVarVariant:53404","phenotype":{"types":[{"id":"HP:0100512","label":"Vitamin D deficiency"}]}},{"entity":"ClinVarVariant:197210","phenotype":{"types":[{"id":"HP:0008261","label":"Pancreatic islet cell adenoma"}]}},{"entity":"MGI:2387852","phenotype":{"types":[{"id":"GO:0070192PHENOTYPE","label":"chromosome organization involved in meiosis phenotype"}]}},{"entity":"FlyBase:FBal0044814","phenotype":{"types":[{"id":"FBbt:00003479PHENOTYPE","label":"Drosophila abdominal ventral muscle phenotype"}]}},{"entity":"ClinVarVariant:177938","phenotype":{"types":[{"id":"HP:0100749","label":"Chest pain"}]}},{"entity":"ClinVarVariant:2139","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ClinVarVariant:24395","phenotype":{"types":[{"id":"HP:0000093","label":"Proteinuria"}]}},{"entity":"MGI:3696958","phenotype":{"types":[{"id":"HP:0100678","label":"Premature skin wrinkling"}]}},{"entity":"ClinVarVariant:36123","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:156339","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:67976","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:157934","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"ClinVarVariant:5408","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:30450","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000209-WBRNAi00073191","phenotype":{"types":[{"id":"WBPhenotype:0001037","label":"sterile progeny"}]}},{"entity":"ClinVarVariant:8814","phenotype":{"types":[{"id":"HP:0004964","label":"Pulmonary arterial medial hypertrophy"}]}},{"entity":"ClinVarVariant:6465","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"MGI:3047647","phenotype":{"types":[{"id":"GO:0043249PHENOTYPE","label":"erythrocyte maturation phenotype"}]}},{"entity":"FlyBase:FBal0204879","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:17309","phenotype":{"types":[{"id":"HP:0007759","label":"Opacification of the corneal stroma"}]}},{"entity":"ClinVarVariant:9368","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:126748","phenotype":{"types":[{"id":"HP:0100760","label":"Clubbing of toes"}]}},{"entity":"ClinVarVariant:161993","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"MGI:2156498","phenotype":{"types":[{"id":"MP:0011086","label":"postnatal lethality, incomplete penetrance"}]}},{"entity":"ClinVarVariant:428","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:53316","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:67838","phenotype":{"types":[{"id":"HP:0004756","label":"Ventricular tachycardia"}]}},{"entity":"ClinVarVariant:211468","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:158542","phenotype":{"types":[{"id":"HP:0010719","label":"Abnormality of hair texture"}]}},{"entity":"ClinVarVariant:158830","phenotype":{"types":[{"id":"HP:0008678","label":"Renal hypoplasia/aplasia"}]}},{"entity":"MGI:1858030","phenotype":{"types":[{"id":"MP:0000819","label":"abnormal olfactory bulb morphology"}]}},{"entity":"MGI:4421413","phenotype":{"types":[{"id":"HP:0011373","label":"Incomplete partition of the cochlea"}]}},{"entity":"ClinVarVariant:25287","phenotype":{"types":[{"id":"HP:0008209","label":"Premature ovarian failure"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004306-WBRNAi00027441","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:161401","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"ClinVarVariant:12010","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"ClinVarVariant:49791","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:49215","phenotype":{"types":[{"id":"HP:0009719","label":"Hypomelanotic macule"}]}},{"entity":"ClinVarVariant:94759","phenotype":{"types":[{"id":"HP:0001644","label":"Dilated cardiomyopathy"}]}},{"entity":"ClinVarVariant:4531","phenotype":{"types":[{"id":"HP:0000144","label":"Decreased fertility"}]}},{"entity":"ClinVarVariant:37353","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:97583","phenotype":{"types":[{"id":"HP:0005214","label":"Intestinal obstruction"}]}},{"entity":"ClinVarVariant:194555","phenotype":{"types":[{"id":"HP:0200134","label":"Epileptic encephalopathy"}]}},{"entity":"FlyBase:FBal0208599","phenotype":{"types":[{"id":"FBcv:0000393","label":"pain response defective"}]}},{"entity":"MGI:5295237","phenotype":{"types":[{"id":"MP:0008498","label":"decreased IgG3 level"}]}},{"entity":"ClinVarVariant:10606","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"MGI:3043578","phenotype":{"types":[{"id":"MP:0001382","label":"abnormal nursing"}]}},{"entity":"ClinVarVariant:10251","phenotype":{"types":[{"id":"HP:0100773","label":"Cartilage destruction"}]}},{"entity":"ClinVarVariant:97709","phenotype":{"types":[{"id":"HP:0001677","label":"Coronary artery disease"}]}},{"entity":"ClinVarVariant:53959","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ClinVarVariant:54093","phenotype":{"types":[{"id":"HP:0000966","label":"Hypohidrosis"}]}},{"entity":"ClinVarVariant:64918","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:4348","phenotype":{"types":[{"id":"HP:0002839","label":"Urinary bladder sphincter dysfunction"}]}},{"entity":"MGI:3610995","phenotype":{"types":[{"id":"MP:0002910","label":"abnormal excitatory postsynaptic currents"}]}},{"entity":"AQTL:55082","phenotype":{"types":[{"id":"AQTLTrait:1153","label":"Stillbirth"}]}},{"entity":"ClinVarVariant:4380","phenotype":{"types":[{"id":"HP:0001281","label":"Tetany"}]}},{"entity":"ClinVarVariant:198424","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"ClinVarVariant:188978","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:6029","phenotype":{"types":[{"id":"HP:0003693","label":"Distal amyotrophy"}]}},{"entity":"ClinVarVariant:5243","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:11483","phenotype":{"types":[{"id":"HP:0003462","label":"Elevated 8-dehydrocholesterol"}]}},{"entity":"ClinVarVariant:49772","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:41177","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"MGI:1857718","phenotype":{"types":[{"id":"MP:0003691","label":"abnormal microglial cell physiology"}]}},{"entity":"ClinVarVariant:158369","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:217105","phenotype":{"types":[{"id":"HP:0001012","label":"Multiple lipomas"}]}},{"entity":"ClinVarVariant:55823","phenotype":{"types":[{"id":"HP:0000864","label":"Abnormality of the hypothalamus-pituitary axis"}]}},{"entity":"ClinVarVariant:14364","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"ClinVarVariant:127699","phenotype":{"types":[{"id":"HP:0002576","label":"Intussusception"}]}},{"entity":"ClinVarVariant:66051","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:4868762","phenotype":{"types":[{"id":"MP:0000428","label":"abnormal craniofacial morphology"}]}},{"entity":"ClinVarVariant:4305","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"MGI:3717494","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"WormBase:WBVar00142947","phenotype":{"types":[{"id":"WBPhenotype:0000644","label":"paralyzed"}]}},{"entity":"dbSNP:rs1896295","phenotype":{"types":[{"id":"HP:0002754","label":"Osteomyelitis"}]}},{"entity":"ClinVarVariant:65505","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:333","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:11675","phenotype":{"types":[{"id":"HP:0000233","label":"Thin vermilion border"}]}},{"entity":"ClinVarVariant:204117","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:8804","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:64705","phenotype":{"types":[{"id":"HP:0009716","label":"Subependymal nodules"}]}},{"entity":"dbSNP:rs1427407","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"FlyBase:FBal0285746","phenotype":{"types":[{"id":"FBbt:00005201PHENOTYPE","label":"denticle belt phenotype"}]}},{"entity":"ClinVarVariant:217428","phenotype":{"types":[{"id":"HP:0001231","label":"Abnormality of the fingernails"}]}},{"entity":"ClinVarVariant:95624","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ZFIN:ZDB-ALT-020426-56","phenotype":{"types":[{"id":"GO:0060036PHENOTYPE","label":"notochord cell vacuolation phenotype"}]}},{"entity":"dbSNP:rs11986414","phenotype":{"types":[{"id":"HP:0002756","label":"Pathologic fracture"}]}},{"entity":"ClinVarVariant:188893","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"ClinVarVariant:7404","phenotype":{"types":[{"id":"HP:0002226","label":"White eyebrow"}]}},{"entity":"ClinVarVariant:25390","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"dbSNP:rs3105491","phenotype":{"types":[{"id":"HP:0004825","label":"Increased hemoglobin oxygen affinity"}]}},{"entity":"ClinVarVariant:204086","phenotype":{"types":[{"id":"HP:0002570","label":"Steatorrhea"}]}},{"entity":"ClinVarVariant:49792","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:136076","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003992-WBRNAi00084326","phenotype":{"types":[{"id":"WBPhenotype:0000061","label":"extended life span"}]}},{"entity":"ClinVarVariant:38917","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:8137","phenotype":{"types":[{"id":"HP:0001002","label":"Decreased subcutaneous fat"}]}},{"entity":"ClinVarVariant:16085","phenotype":{"types":[{"id":"HP:0000055","label":"Abnormality of female external genitalia"}]}},{"entity":"ClinVarVariant:11362","phenotype":{"types":[{"id":"HP:0200042","label":"Skin ulcer"}]}},{"entity":"ClinVarVariant:101206","phenotype":{"types":[{"id":"HP:0000023","label":"Inguinal hernia"}]}},{"entity":"ClinVarVariant:53224","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:39727","phenotype":{"types":[{"id":"HP:0002239","label":"Gastrointestinal hemorrhage"}]}},{"entity":"ClinVarVariant:21106","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:91405","phenotype":{"types":[{"id":"HP:0002472","label":"Small cerebral cortex"}]}},{"entity":"FlyBase:FBal0144279","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011897-WBRNAi00095734","phenotype":{"types":[{"id":"WBPhenotype:0000402","label":"avoids bacterial lawn"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008149-WBRNAi00029911","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"ClinVarVariant:161364","phenotype":{"types":[{"id":"HP:0002486","label":"Myotonia"}]}},{"entity":"ClinVarVariant:2249","phenotype":{"types":[{"id":"HP:0001287","label":"Meningitis"}]}},{"entity":"FlyBase:FBal0270164","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:56689","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:102786","phenotype":{"types":[{"id":"HP:0005599","label":"Hypopigmentation of hair"}]}},{"entity":"ClinVarVariant:25221","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"AQTL:39589","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"dbSNP:rs10005603","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:35514","phenotype":{"types":[{"id":"HP:0000622","label":"Blurred vision"}]}},{"entity":"ClinVarVariant:179339","phenotype":{"types":[{"id":"HP:0001696","label":"Situs inversus totalis"}]}},{"entity":"ClinVarVariant:52328","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"dbSNP:rs6545883","phenotype":{"types":[{"id":"HP:0008207","label":"Primary adrenal insufficiency"}]}},{"entity":"AQTL:16175","phenotype":{"types":[{"id":"AQTLTrait:1044","label":"Milk yield"}]}},{"entity":"WormBase:WBVar00242144","phenotype":{"types":[{"id":"WBPhenotype:0000116","label":"mid larval lethal"}]}},{"entity":"ClinVarVariant:53973","phenotype":{"types":[{"id":"HP:0100582","label":"Nasal polyposis"}]}},{"entity":"ClinVarVariant:10872","phenotype":{"types":[{"id":"HP:0000286","label":"Epicanthus"}]}},{"entity":"ClinVarVariant:159191","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"ClinVarVariant:210786","phenotype":{"types":[{"id":"HP:0005306","label":"Capillary hemangiomas"}]}},{"entity":"ClinVarVariant:133075","phenotype":{"types":[{"id":"HP:0003738","label":"Exercise-induced myalgia"}]}},{"entity":"ClinVarVariant:211503","phenotype":{"types":[{"id":"HP:0000171","label":"Microglossia"}]}},{"entity":"ClinVarVariant:21274","phenotype":{"types":[{"id":"HP:0002827","label":"Hip dislocation"}]}},{"entity":"ClinVarVariant:14662","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:189027","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"MGI:3777553","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:16869","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ZFIN:ZDB-ALT-090625-1","phenotype":{"types":[{"id":"ZP:0004126","label":"abnormal(ly) absent intrahepatic bile duct"}]}},{"entity":"ClinVarVariant:35575","phenotype":{"types":[{"id":"HP:0001061","label":"Acne"}]}},{"entity":"ClinVarVariant:41181","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:7435","phenotype":{"types":[{"id":"HP:0000581","label":"Blepharophimosis"}]}},{"entity":"ClinVarVariant:56414","phenotype":{"types":[{"id":"HP:0003452","label":"Increased serum iron"}]}},{"entity":"ClinVarVariant:11159","phenotype":{"types":[{"id":"HP:0011948","label":"Acute respiratory tract infection"}]}},{"entity":"MGI:5311612","phenotype":{"types":[{"id":"MP:0002080","label":"prenatal lethality"}]}},{"entity":"ClinVarVariant:5116","phenotype":{"types":[{"id":"HP:0002857","label":"Genu valgum"}]}},{"entity":"ClinVarVariant:198034","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"FlyBase:FBal0244011","phenotype":{"types":[{"id":"FBbt:00004233PHENOTYPE","label":"Drosophila tertiary pigment cell phenotype"}]}},{"entity":"ClinVarVariant:97913","phenotype":{"types":[{"id":"HP:0001917","label":"Renal amyloidosis"}]}},{"entity":"ClinVarVariant:159983","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"ClinVarVariant:157955","phenotype":{"types":[{"id":"HP:0100022","label":"Abnormality of movement"}]}},{"entity":"ClinVarVariant:38312","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:158564","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"MGI:2674291","phenotype":{"types":[{"id":"MP:0000031","label":"abnormal cochlea morphology"}]}},{"entity":"ClinVarVariant:7230","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"NCBIGene:7467","phenotype":{"types":[{"id":"HP:0009778","label":"Short thumb"}]}},{"entity":"ClinVarVariant:56562","phenotype":{"types":[{"id":"HP:0000457","label":"Depressed nasal ridge"}]}},{"entity":"ClinVarVariant:155828","phenotype":{"types":[{"id":"HP:0000189","label":"Narrow palate"}]}},{"entity":"ClinVarVariant:182975","phenotype":{"types":[{"id":"HP:0002666","label":"Pheochromocytoma"}]}},{"entity":"FlyBase:FBal0206553","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:53925","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"NCBIGene:140906","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"FlyBase:FBal0159762","phenotype":{"types":[{"id":"FBbt:00005838PHENOTYPE","label":"NMJ bouton phenotype"}]}},{"entity":"ClinVarVariant:96117","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:14347","phenotype":{"types":[{"id":"HP:0002013","label":"Vomiting"}]}},{"entity":"ClinVarVariant:41334","phenotype":{"types":[{"id":"HP:0007067","label":"Distal peripheral sensory neuropathy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019801-WBRNAi00082236","phenotype":{"types":[{"id":"WBPhenotype:0001541","label":"dauer gonad arrest variant"}]}},{"entity":"ClinVarVariant:49738","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"MGI:2388352","phenotype":{"types":[{"id":"MP:0001274","label":"curly vibrissae"}]}},{"entity":"MGI:3690317","phenotype":{"types":[{"id":"HP:0012184","label":"Hyperalphalipoproteinemia"}]}},{"entity":"ClinVarVariant:159478","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"ClinVarVariant:4296","phenotype":{"types":[{"id":"HP:0011857","label":"Plasmacytoma"}]}},{"entity":"ClinVarVariant:53697","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019268-WBRNAi00008936","phenotype":{"types":[{"id":"WBPhenotype:0000032","label":"sick"}]}},{"entity":"ClinVarVariant:181743","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:1381","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"MGI:5520177","phenotype":{"types":[{"id":"HP:0000752","label":"Hyperactivity"}]}},{"entity":"FlyBase:FBal0208692","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:4613","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"MGI:1857196","phenotype":{"types":[{"id":"MP:0006082","label":"CNS inflammation"}]}},{"entity":"ClinVarVariant:216024","phenotype":{"types":[{"id":"HP:0002073","label":"Progressive cerebellar ataxia"}]}},{"entity":"ClinVarVariant:101299","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:36103","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:36315","phenotype":{"types":[{"id":"HP:0001025","label":"Urticaria"}]}},{"entity":"ClinVarVariant:181495","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:11362","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"FlyBase:FBal0147448","phenotype":{"types":[{"id":"FBcv:0000414","label":"locomotor behavior defective"}]}},{"entity":"ClinVarVariant:180350","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:1185","phenotype":{"types":[{"id":"HP:0000013","label":"Hypoplasia of the uterus"}]}},{"entity":"FlyBase:FBal0305239","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"dbSNP:rs41648982","phenotype":{"types":[{"id":"AQTLTrait:1120","label":"Thurl width"}]}},{"entity":"ClinVarVariant:159128","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"ClinVarVariant:6097","phenotype":{"types":[{"id":"HP:0006315","label":"Single median maxillary incisor"}]}},{"entity":"ClinVarVariant:10219","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:188945","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:101148","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00014088-WBRNAi00027107","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:53370","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:38995","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"dbSNP:rs109034504","phenotype":{"types":[{"id":"AQTLTrait:1070","label":"Inseminations per conception"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003026-WBRNAi00085490","phenotype":{"types":[{"id":"WBPhenotype:0001973","label":"germ cell compartment size variant"}]}},{"entity":"ClinVarVariant:18346","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:6094","phenotype":{"types":[{"id":"HP:0000748","label":"Inappropriate laughter"}]}},{"entity":"ClinVarVariant:56708","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"FlyBase:FBal0181584","phenotype":{"types":[{"id":"FBcv:0000450","label":"developmental rate defective"}]}},{"entity":"ClinVarVariant:159663","phenotype":{"types":[{"id":"HP:0006461","label":"Proximal femoral epiphysiolysis"}]}},{"entity":"MGI:104735","phenotype":{"types":[{"id":"MP:0002169","label":"no abnormal phenotype detected"}]}},{"entity":"ClinVarVariant:30538","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:17168","phenotype":{"types":[{"id":"HP:0006149","label":"Increased laxity of fingers"}]}},{"entity":"FlyBase:FBal0058344","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:21208","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:29973","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:2618","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:68708","phenotype":{"types":[{"id":"HP:0002900","label":"Hypokalemia"}]}},{"entity":"MGI:3620798","phenotype":{"types":[{"id":"MP:0002410","label":"decreased susceptibility to viral infection"}]}},{"entity":"MGI:3774341","phenotype":{"types":[{"id":"MP:0003203","label":"increased neuron apoptosis"}]}},{"entity":"ClinVarVariant:6552","phenotype":{"types":[{"id":"HP:0002213","label":"Fine hair"}]}},{"entity":"ClinVarVariant:56706","phenotype":{"types":[{"id":"HP:0002074","label":"Increased neuronal autofluorescent lipopigment"}]}},{"entity":"ClinVarVariant:40494","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"ClinVarVariant:10299","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:3050446","phenotype":{"types":[{"id":"MP:0004564","label":"enlarged myocardial fiber"}]}},{"entity":"ClinVarVariant:209062","phenotype":{"types":[{"id":"HP:0002107","label":"Pneumothorax"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001031-WBRNAi00072843","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:53980","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"ClinVarVariant:36058","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"AQTL:16912","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:211716","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:9319","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:30750","phenotype":{"types":[{"id":"HP:0003228","label":"Hypernatremia"}]}},{"entity":"ClinVarVariant:188958","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:211640","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:35842","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"ClinVarVariant:162384","phenotype":{"types":[{"id":"HP:0008070","label":"Sparse hair"}]}},{"entity":"MGI:5430994","phenotype":{"types":[{"id":"HP:0005576","label":"Tubulointerstitial fibrosis"}]}},{"entity":"ClinVarVariant:5645","phenotype":{"types":[{"id":"HP:0030507","label":"Retinal crystals"}]}},{"entity":"ClinVarVariant:40164","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00077457-WBRNAi00063328","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:14209","phenotype":{"types":[{"id":"HP:0000960","label":"Sacral dimple"}]}},{"entity":"ClinVarVariant:14097","phenotype":{"types":[{"id":"HP:0001712","label":"Left ventricular hypertrophy"}]}},{"entity":"ClinVarVariant:198504","phenotype":{"types":[{"id":"HP:0008443","label":"Spinal deformities"}]}},{"entity":"MGI:3695137","phenotype":{"types":[{"id":"MP:0005463","label":"abnormal CD4-positive, alpha-beta T cell physiology"}]}},{"entity":"ClinVarVariant:6067","phenotype":{"types":[{"id":"HP:0200055","label":"Small hand"}]}},{"entity":"ClinVarVariant:2669","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:97554","phenotype":{"types":[{"id":"HP:0000999","label":"Pyoderma"}]}},{"entity":"ClinVarVariant:24752","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:67777","phenotype":{"types":[{"id":"HP:0001696","label":"Situs inversus totalis"}]}},{"entity":"ClinVarVariant:6820","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"AQTL:41673","phenotype":{"types":[{"id":"AQTLTrait:1136","label":"Bone quality"}]}},{"entity":"ClinVarVariant:14209","phenotype":{"types":[{"id":"HP:0001875","label":"Neutropenia"}]}},{"entity":"ClinVarVariant:36946","phenotype":{"types":[{"id":"HP:0001915","label":"Aplastic anemia"}]}},{"entity":"ClinVarVariant:210456","phenotype":{"types":[{"id":"HP:0003819","label":"Death in childhood"}]}},{"entity":"ClinVarVariant:30945","phenotype":{"types":[{"id":"HP:0000388","label":"Otitis media"}]}},{"entity":"ClinVarVariant:49452","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:181763","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:6625","phenotype":{"types":[{"id":"HP:0000998","label":"Hypertrichosis"}]}},{"entity":"ClinVarVariant:83156","phenotype":{"types":[{"id":"HP:0006740","label":"Transitional cell carcinoma of the bladder"}]}},{"entity":"ClinVarVariant:36913","phenotype":{"types":[{"id":"HP:0002664","label":"Neoplasm"}]}},{"entity":"ClinVarVariant:42284","phenotype":{"types":[{"id":"HP:0004935","label":"Pulmonary artery atresia"}]}},{"entity":"MGI:1888408","phenotype":{"types":[{"id":"MP:0005641","label":"increased mean corpuscular hemoglobin concentration"}]}},{"entity":"ClinVarVariant:17696","phenotype":{"types":[{"id":"HP:0004370","label":"Abnormality of temperature regulation"}]}},{"entity":"ClinVarVariant:211746","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:25350","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:53346","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:13346","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"FlyBase:FBal0205447","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:65275","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"ClinVarVariant:53784","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:16623","phenotype":{"types":[{"id":"HP:0001371","label":"Flexion contracture"}]}},{"entity":"ClinVarVariant:48902","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"ClinVarVariant:189811","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:53373","phenotype":{"types":[{"id":"HP:0006706","label":"Cystic liver disease"}]}},{"entity":"ClinVarVariant:53337","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"MGI:4868451","phenotype":{"types":[{"id":"GO:0021697PHENOTYPE","label":"cerebellar cortex formation phenotype"}]}},{"entity":"AQTL:27090","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:92715","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:91403","phenotype":{"types":[{"id":"HP:0008678","label":"Renal hypoplasia/aplasia"}]}},{"entity":"ClinVarVariant:42015","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:68718","phenotype":{"types":[{"id":"HP:0002900","label":"Hypokalemia"}]}},{"entity":"ClinVarVariant:136097","phenotype":{"types":[{"id":"HP:0001166","label":"Arachnodactyly"}]}},{"entity":"ClinVarVariant:93448","phenotype":{"types":[{"id":"HP:0003271","label":"Visceromegaly"}]}},{"entity":"ClinVarVariant:10158","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"ClinVarVariant:188958","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"FlyBase:FBal0093398","phenotype":{"types":[{"id":"FBbt:00007115PHENOTYPE","label":"embryonic/larval neuroblast phenotype"}]}},{"entity":"ClinVarVariant:6066","phenotype":{"types":[{"id":"HP:0011318","label":"Bicoronal synostosis"}]}},{"entity":"ClinVarVariant:12534","phenotype":{"types":[{"id":"HP:0004493","label":"Craniofacial hyperostosis"}]}},{"entity":"ClinVarVariant:25214","phenotype":{"types":[{"id":"HP:0010741","label":"Edema of the lower limbs"}]}},{"entity":"FlyBase:FBal0263650","phenotype":{"types":[{"id":"FBbt:00004193PHENOTYPE","label":"cone cell phenotype"}]}},{"entity":"ClinVarVariant:53702","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"ClinVarVariant:2691","phenotype":{"types":[{"id":"HP:0011073","label":"Abnormality of dental color"}]}},{"entity":"ClinVarVariant:2143","phenotype":{"types":[{"id":"HP:0003083","label":"Dislocated radial head"}]}},{"entity":"ClinVarVariant:54083","phenotype":{"types":[{"id":"HP:0004401","label":"Meconium ileus"}]}},{"entity":"ClinVarVariant:35862","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"ClinVarVariant:158299","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:11515","phenotype":{"types":[{"id":"HP:0004594","label":"Hump-shaped mound of bone in central and posterior portions of vertebral endplate"}]}},{"entity":"ClinVarVariant:189750","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:16425","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"ClinVarVariant:60494","phenotype":{"types":[{"id":"HP:0002652","label":"Skeletal dysplasia"}]}},{"entity":"ClinVarVariant:216824","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:12281","phenotype":{"types":[{"id":"HP:0002908","label":"Conjugated hyperbilirubinemia"}]}},{"entity":"AQTL:46013","phenotype":{"types":[{"id":"AQTLTrait:1115","label":"Chest width"}]}},{"entity":"ClinVarVariant:135760","phenotype":{"types":[{"id":"HP:0012189","label":"Hodgkin lymphoma"}]}},{"entity":"MGI:5510759","phenotype":{"types":[{"id":"MP:0004794","label":"increased anti-nuclear antigen antibody level"}]}},{"entity":"MGI:2679886","phenotype":{"types":[{"id":"HP:0002011","label":"Morphological abnormality of the central nervous system"}]}},{"entity":"MGI:1857437","phenotype":{"types":[{"id":"MP:0003477","label":"abnormal nerve fiber response"}]}},{"entity":"MGI:1931041","phenotype":{"types":[{"id":"MP:0013164","label":"abnormal forelimb bud morphology"}]}},{"entity":"ClinVarVariant:56445","phenotype":{"types":[{"id":"HP:0003077","label":"Hyperlipidemia"}]}},{"entity":"ClinVarVariant:21512","phenotype":{"types":[{"id":"HP:0003233","label":"Hypoalphalipoproteinemia"}]}},{"entity":"ClinVarVariant:50091","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:2149","phenotype":{"types":[{"id":"HP:0000089","label":"Renal hypoplasia"}]}},{"entity":"ClinVarVariant:143395","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:30199","phenotype":{"types":[{"id":"HP:0001220","label":"Interphalangeal joint contracture of finger"}]}},{"entity":"ClinVarVariant:12524","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:36101","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:139581","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"ClinVarVariant:211726","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"FlyBase:FBal0150725","phenotype":{"types":[{"id":"FBbt:00003361PHENOTYPE","label":"indirect flight muscle phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019218-WBRNAi00086983","phenotype":{"types":[{"id":"WBPhenotype:0000038","label":"exploded through vulva"}]}},{"entity":"ClinVarVariant:216978","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"FlyBase:FBal0189919","phenotype":{"types":[{"id":"FBcv:0000356","label":"body color defective"}]}},{"entity":"ClinVarVariant:12048","phenotype":{"types":[{"id":"HP:0004947","label":"Arteriovenous fistula"}]}},{"entity":"ClinVarVariant:25350","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:5983","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:9521","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:5198","phenotype":{"types":[{"id":"HP:0100261","label":"Abnormal tendon morphology"}]}},{"entity":"ClinVarVariant:179126","phenotype":{"types":[{"id":"HP:0003805","label":"Rimmed vacuoles"}]}},{"entity":"MGI:1857150","phenotype":{"types":[{"id":"MP:0006413","label":"increased T cell apoptosis"}]}},{"entity":"MGI:3833397","phenotype":{"types":[{"id":"HP:0100763","label":"Abnormality of the lymphatic system"}]}},{"entity":"ClinVarVariant:3364","phenotype":{"types":[{"id":"HP:0200040","label":"Epidermoid cyst"}]}},{"entity":"MGI:3613611","phenotype":{"types":[{"id":"MP:0002836","label":"abnormal chorion morphology"}]}},{"entity":"ClinVarVariant:50874","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"FlyBase:FBal0283530","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"AQTL:50857","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"dbSNP:rs12386026","phenotype":{"types":[{"id":"HP:0001510","label":"Growth delay"}]}},{"entity":"ClinVarVariant:30725","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:11422","phenotype":{"types":[{"id":"HP:0011003","label":"Severe Myopia"}]}},{"entity":"ClinVarVariant:2915","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1443","phenotype":{"types":[{"id":"ZP:0001246","label":"abnormal(ly) morphology inner ear"}]}},{"entity":"MGI:2387973","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:53725","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"MGI:2386460","phenotype":{"types":[{"id":"MP:0000880","label":"decreased Purkinje cell number"}]}},{"entity":"ClinVarVariant:189842","phenotype":{"types":[{"id":"HP:0002384","label":"Focal seizures with impairment of consciousness or awareness"}]}},{"entity":"ClinVarVariant:162019","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:9590","phenotype":{"types":[{"id":"HP:0000762","label":"Decreased nerve conduction velocity"}]}},{"entity":"ClinVarVariant:53660","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"MGI:3628446","phenotype":{"types":[{"id":"MP:0004379","label":"wide frontal bone"}]}},{"entity":"ClinVarVariant:16330","phenotype":{"types":[{"id":"HP:0000256","label":"Macrocephaly"}]}},{"entity":"ClinVarVariant:2577","phenotype":{"types":[{"id":"HP:0000660","label":"Lipemia retinalis"}]}},{"entity":"ClinVarVariant:157514","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"ClinVarVariant:2627","phenotype":{"types":[{"id":"HP:0010743","label":"Short metatarsal"}]}},{"entity":"ClinVarVariant:10194","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:88859","phenotype":{"types":[{"id":"HP:0000091","label":"Abnormality of the renal tubule"}]}},{"entity":"ClinVarVariant:56718","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"ClinVarVariant:53254","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:3792","phenotype":{"types":[{"id":"HP:0001022","label":"Albinism"}]}},{"entity":"ClinVarVariant:53912","phenotype":{"types":[{"id":"HP:0001082","label":"Cholecystitis"}]}},{"entity":"ClinVarVariant:42566","phenotype":{"types":[{"id":"HP:0001297","label":"Stroke"}]}},{"entity":"ClinVarVariant:10669","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:6895","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"ClinVarVariant:12414","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"WormBase:WBVar01473710","phenotype":{"types":[{"id":"WBPhenotype:0000643","label":"locomotion variant"}]}},{"entity":"ClinVarVariant:182828","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:7984","phenotype":{"types":[{"id":"HP:0003189","label":"Long nose"}]}},{"entity":"ClinVarVariant:186330","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"MGI:3702746","phenotype":{"types":[{"id":"HP:0012087","label":"Abnormal mitochondrial shape"}]}},{"entity":"ClinVarVariant:216684","phenotype":{"types":[{"id":"HP:0000020","label":"Urinary incontinence"}]}},{"entity":"ClinVarVariant:65134","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:65092","phenotype":{"types":[{"id":"HP:0009719","label":"Hypomelanotic macule"}]}},{"entity":"ClinVarVariant:101385","phenotype":{"types":[{"id":"HP:0005293","label":"Venous insufficiency"}]}},{"entity":"ClinVarVariant:159912","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:181753","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"WormBase:WBVar00240990","phenotype":{"types":[{"id":"MP:0002209","label":"decreased germ cell number"}]}},{"entity":"ClinVarVariant:21729","phenotype":{"types":[{"id":"HP:0001080","label":"Biliary tract abnormality"}]}},{"entity":"ClinVarVariant:180360","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:53458","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"ClinVarVariant:6668","phenotype":{"types":[{"id":"HP:0009025","label":"Increased connective tissue"}]}},{"entity":"ClinVarVariant:2086","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"AQTL:12518","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"ClinVarVariant:54185","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:3965","phenotype":{"types":[{"id":"HP:0007633","label":"Bilateral microphthalmos"}]}},{"entity":"AQTL:26646","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:210770","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:166724","phenotype":{"types":[{"id":"HP:0003774","label":"Stage 5 chronic kidney disease"}]}},{"entity":"ClinVarVariant:143294","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"ClinVarVariant:36126","phenotype":{"types":[{"id":"HP:0008132","label":"Medial rotation of the medial malleolus"}]}},{"entity":"ClinVarVariant:36092","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:53574","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"ClinVarVariant:158741","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:12780","phenotype":{"types":[{"id":"HP:0006880","label":"Cerebellar hemangioblastoma"}]}},{"entity":"ClinVarVariant:21545","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1436","phenotype":{"types":[{"id":"ZP:0007196","label":"abnormal(ly) structure optic tract"}]}},{"entity":"ClinVarVariant:167709","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:35830","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:49922","phenotype":{"types":[{"id":"HP:0006772","label":"Renal angiomyolipoma"}]}},{"entity":"ClinVarVariant:6384","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"MGI:1933835","phenotype":{"types":[{"id":"MP:0010500","label":"myocardium hypoplasia"}]}},{"entity":"MGI:1857208","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:67907","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"FlyBase:FBal0210831","phenotype":{"types":[{"id":"FBcv:0000665","label":"body size defective"}]}},{"entity":"ClinVarVariant:136160","phenotype":{"types":[{"id":"HP:0001679","label":"Abnormality of the aorta"}]}},{"entity":"AQTL:39150","phenotype":{"types":[{"id":"AQTLTrait:1096","label":"Teat length"}]}},{"entity":"ClinVarVariant:48426","phenotype":{"types":[{"id":"HP:0010780","label":"Hyperacusis"}]}},{"entity":"ClinVarVariant:100768","phenotype":{"types":[{"id":"HP:0011448","label":"Ankle clonus"}]}},{"entity":"ClinVarVariant:158764","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"dbSNP:rs1934954","phenotype":{"types":[{"id":"HP:0000988","label":"Skin rash"}]}},{"entity":"ClinVarVariant:53774","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:1965","phenotype":{"types":[{"id":"HP:0001890","label":"Autoimmune hemolytic anemia"}]}},{"entity":"ClinVarVariant:215590","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:6542","phenotype":{"types":[{"id":"HP:0002213","label":"Fine hair"}]}},{"entity":"ClinVarVariant:39867","phenotype":{"types":[{"id":"HP:0002910","label":"Elevated hepatic transaminases"}]}},{"entity":"ClinVarVariant:53327","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"ClinVarVariant:14005","phenotype":{"types":[{"id":"HP:0100783","label":"Breast aplasia"}]}},{"entity":"ClinVarVariant:189048","phenotype":{"types":[{"id":"HP:0005598","label":"Facial telangiectasia in butterfly midface distribution"}]}},{"entity":"ZFIN:ZDB-ALT-051223-6","phenotype":{"types":[{"id":"ZP:0011581","label":"abnormal(ly) malformed post-vent vasculature"}]}},{"entity":"ClinVarVariant:16685","phenotype":{"types":[{"id":"HP:0002027","label":"Abdominal pain"}]}},{"entity":"ClinVarVariant:9659","phenotype":{"types":[{"id":"HP:0002891","label":"Uterine leiomyosarcoma"}]}},{"entity":"MGI:1857211","phenotype":{"types":[{"id":"MP:0008070","label":"absent T cells"}]}},{"entity":"ClinVarVariant:13370","phenotype":{"types":[{"id":"HP:0001894","label":"Thrombocytosis"}]}},{"entity":"ClinVarVariant:53565","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"ClinVarVariant:216937","phenotype":{"types":[{"id":"HP:0006960","label":"Choroid plexus calcification"}]}},{"entity":"MGI:3529581","phenotype":{"types":[{"id":"MP:0009967","label":"abnormal neuron proliferation"}]}},{"entity":"MGI:2156458","phenotype":{"types":[{"id":"HP:0006270","label":"Hypoplastic spleen"}]}},{"entity":"ClinVarVariant:68700","phenotype":{"types":[{"id":"HP:0000843","label":"Hyperparathyroidism"}]}},{"entity":"ClinVarVariant:53326","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:161123","phenotype":{"types":[{"id":"HP:0000496","label":"Abnormality of eye movement"}]}},{"entity":"ClinVarVariant:10486","phenotype":{"types":[{"id":"HP:0001922","label":"Vacuolated lymphocytes"}]}},{"entity":"ClinVarVariant:53236","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:24442","phenotype":{"types":[{"id":"HP:0008619","label":"Bilateral sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:4617","phenotype":{"types":[{"id":"HP:0003390","label":"Sensory axonal neuropathy"}]}},{"entity":"ClinVarVariant:101415","phenotype":{"types":[{"id":"HP:0000963","label":"Thin skin"}]}},{"entity":"FlyBase:FBal0239918","phenotype":{"types":[{"id":"FBcv:0000408","label":"stress response defective"}]}},{"entity":"ClinVarVariant:42377","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"dbSNP:rs110204815","phenotype":{"types":[{"id":"AQTLTrait:1081","label":"Age at puberty"}]}},{"entity":"ClinVarVariant:3694","phenotype":{"types":[{"id":"HP:0001114","label":"Xanthelasma"}]}},{"entity":"FlyBase:FBal0038994","phenotype":{"types":[{"id":"FBbt:00002142PHENOTYPE","label":"Drosophila metathoracic intersegmental nerve phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008852-WBRNAi00093225","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"ClinVarVariant:35521","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:36133","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:181833","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"ClinVarVariant:25300","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"AQTL:23571","phenotype":{"types":[{"id":"AQTLTrait:2252","label":"LDL cholesterol level"}]}},{"entity":"ClinVarVariant:159421","phenotype":{"types":[{"id":"HP:0100627","label":"Displacement of the external urethral meatus"}]}},{"entity":"MGI:2389580","phenotype":{"types":[{"id":"MP:0000952","label":"abnormal CNS glial cell morphology"}]}},{"entity":"ClinVarVariant:100651","phenotype":{"types":[{"id":"HP:0002553","label":"Highly arched eyebrow"}]}},{"entity":"FlyBase:FBal0277412","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:135775","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:189124","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:42053","phenotype":{"types":[{"id":"HP:0003281","label":"Increased serum ferritin"}]}},{"entity":"ClinVarVariant:18426","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:5965","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"ClinVarVariant:10867","phenotype":{"types":[{"id":"HP:0010972","label":"Anemia of inadequate production"}]}},{"entity":"ClinVarVariant:24410","phenotype":{"types":[{"id":"HP:0100633","label":"Esophagitis"}]}},{"entity":"AQTL:7240","phenotype":{"types":[{"id":"AQTLTrait:554","label":"Anal atresia"}]}},{"entity":"ClinVarVariant:97813","phenotype":{"types":[{"id":"HP:0001974","label":"Leukocytosis"}]}},{"entity":"ClinVarVariant:3642","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:49340","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"ClinVarVariant:24295","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"MGI:4849540","phenotype":{"types":[{"id":"MP:0009420","label":"skeletal muscle endomysial fibrosis"}]}},{"entity":"FlyBase:FBal0204839","phenotype":{"types":[{"id":"FBbt:00004729PHENOTYPE","label":"Drosophila wing phenotype"}]}},{"entity":"ClinVarVariant:96617","phenotype":{"types":[{"id":"HP:0006846","label":"Acute encephalopathy"}]}},{"entity":"ClinVarVariant:135766","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:38889","phenotype":{"types":[{"id":"HP:0002634","label":"Arteriosclerosis"}]}},{"entity":"MGI:1856150","phenotype":{"types":[{"id":"MP:0000159","label":"abnormal xiphoid process morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004887-WBRNAi00030287","phenotype":{"types":[{"id":"WBPhenotype:0000054","label":"larval lethal"}]}},{"entity":"ClinVarVariant:15282","phenotype":{"types":[{"id":"HP:0005505","label":"Refractory anemia"}]}},{"entity":"ClinVarVariant:21759","phenotype":{"types":[{"id":"HP:0002411","label":"Myokymia"}]}},{"entity":"AQTL:42663","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"ClinVarVariant:11445","phenotype":{"types":[{"id":"HP:0002136","label":"Broad-based gait"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001486-WBRNAi00102268","phenotype":{"types":[{"id":"WBPhenotype:0001900","label":"reduced levels of reduced glutathione"}]}},{"entity":"ClinVarVariant:194287","phenotype":{"types":[{"id":"HP:0004404","label":"Abnormality of the nipple"}]}},{"entity":"ClinVarVariant:167080","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:65853","phenotype":{"types":[{"id":"HP:0001274","label":"Agenesis of corpus callosum"}]}},{"entity":"ClinVarVariant:101152","phenotype":{"types":[{"id":"HP:0000490","label":"Deeply set eye"}]}},{"entity":"ClinVarVariant:180194","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"ClinVarVariant:60506","phenotype":{"types":[{"id":"HP:0003510","label":"Severe short stature"}]}},{"entity":"ClinVarVariant:159910","phenotype":{"types":[{"id":"HP:0003881","label":"Humeral sclerosis"}]}},{"entity":"FlyBase:FBal0244148","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:53229","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"AQTL:408","phenotype":{"types":[{"id":"AQTLTrait:2056","label":"Skin fat weight"}]}},{"entity":"NCBIGene:100302680","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"MGI:4429538","phenotype":{"types":[{"id":"MP:0008025","label":"brain vacuoles"}]}},{"entity":"ClinVarVariant:65014","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:162525","phenotype":{"types":[{"id":"HP:0008281","label":"Acute hyperammonemia"}]}},{"entity":"ClinVarVariant:157514","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001177-WBRNAi00061092","phenotype":{"types":[{"id":"WBPhenotype:0000279","label":"spicule insertion defective"}]}},{"entity":"FlyBase:FBal0258005","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:53758","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:53983","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:53422","phenotype":{"types":[{"id":"HP:0001948","label":"Alkalosis"}]}},{"entity":"FlyBase:FBal0042573","phenotype":{"types":[{"id":"FBbt:00000008PHENOTYPE","label":"Drosophila labral segment phenotype"}]}},{"entity":"ClinVarVariant:41171","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:188881","phenotype":{"types":[{"id":"HP:0001874","label":"Abnormality of neutrophils"}]}},{"entity":"ClinVarVariant:40291","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:7502","phenotype":{"types":[{"id":"HP:0007468","label":"Perifollicular hyperkeratosis"}]}},{"entity":"ClinVarVariant:7725","phenotype":{"types":[{"id":"HP:0007552","label":"Abnormal subcutaneous fat tissue distribution"}]}},{"entity":"ClinVarVariant:11577","phenotype":{"types":[{"id":"HP:0007018","label":"Attention deficit hyperactivity disorder"}]}},{"entity":"MGI:3771073","phenotype":{"types":[{"id":"MP:0003017","label":"decreased circulating bicarbonate level"}]}},{"entity":"ClinVarVariant:13335","phenotype":{"types":[{"id":"HP:0001644","label":"Dilated cardiomyopathy"}]}},{"entity":"ClinVarVariant:53336","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:49180","phenotype":{"types":[{"id":"HP:0010762","label":"Chordoma"}]}},{"entity":"ClinVarVariant:52318","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"MGI:1857270","phenotype":{"types":[{"id":"MP:0002655","label":"abnormal keratinocyte morphology"}]}},{"entity":"ClinVarVariant:161210","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:162038","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:31100","phenotype":{"types":[{"id":"HP:0002558","label":"Supernumerary nipple"}]}},{"entity":"ClinVarVariant:41098","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:167222","phenotype":{"types":[{"id":"HP:0002566","label":"Intestinal malrotation"}]}},{"entity":"ClinVarVariant:216765","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:10753","phenotype":{"types":[{"id":"HP:0012622","label":"Chronic kidney disease"}]}},{"entity":"ClinVarVariant:53982","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:184580","phenotype":{"types":[{"id":"HP:0100777","label":"Exostoses"}]}},{"entity":"ClinVarVariant:8986","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007704-WBRNAi00066087","phenotype":{"types":[{"id":"WBPhenotype:0000541","label":"cord commissures fail to reach target"}]}},{"entity":"MGI:2681122","phenotype":{"types":[{"id":"MP:0003868","label":"abnormal feces composition"}]}},{"entity":"dbSNP:rs6538140","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:53000","phenotype":{"types":[{"id":"HP:0000598","label":"Abnormality of the ear"}]}},{"entity":"ClinVarVariant:158819","phenotype":{"types":[{"id":"HP:0000340","label":"Sloping forehead"}]}},{"entity":"ClinVarVariant:15202","phenotype":{"types":[{"id":"HP:0008151","label":"Prolonged prothrombin time"}]}},{"entity":"MGI:2385836","phenotype":{"types":[{"id":"MP:0004087","label":"abnormal muscle fiber morphology"}]}},{"entity":"ClinVarVariant:3961","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:38352","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:8870","phenotype":{"types":[{"id":"HP:0001216","label":"Delayed ossification of carpal bones"}]}},{"entity":"ClinVarVariant:10053","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:49410","phenotype":{"types":[{"id":"HP:0002617","label":"Aneurysm"}]}},{"entity":"ClinVarVariant:49858","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"MGI:3838346","phenotype":{"types":[{"id":"MP:0003917","label":"increased kidney weight"}]}},{"entity":"MGI:2181194","phenotype":{"types":[{"id":"MP:0010970","label":"abnormal compact bone lamellar structure"}]}},{"entity":"ClinVarVariant:53813","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:6278","phenotype":{"types":[{"id":"HP:0011362","label":"Abnormal hair quantity"}]}},{"entity":"ClinVarVariant:24558","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"MGI:4843437","phenotype":{"types":[{"id":"MP:0010268","label":"decreased lymphoma incidence"}]}},{"entity":"ClinVarVariant:7993","phenotype":{"types":[{"id":"HP:0000912","label":"Sprengel anomaly"}]}},{"entity":"ClinVarVariant:11313","phenotype":{"types":[{"id":"HP:0003455","label":"Elevated long chain fatty acids"}]}},{"entity":"AQTL:13657","phenotype":{"types":[{"id":"AQTLTrait:1086","label":"Udder structure"}]}},{"entity":"ClinVarVariant:66802","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:42315","phenotype":{"types":[{"id":"HP:0004933","label":"Ascending aortic dissection"}]}},{"entity":"ClinVarVariant:2827","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"ClinVarVariant:127449","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"MGI:3845884","phenotype":{"types":[{"id":"MP:0008019","label":"increased liver tumor incidence"}]}},{"entity":"ClinVarVariant:210769","phenotype":{"types":[{"id":"HP:0000336","label":"Prominent supraorbital ridges"}]}},{"entity":"ClinVarVariant:14051","phenotype":{"types":[{"id":"HP:0002359","label":"Frequent falls"}]}},{"entity":"ClinVarVariant:7224","phenotype":{"types":[{"id":"HP:0100651","label":"Type I diabetes mellitus"}]}},{"entity":"ClinVarVariant:196495","phenotype":{"types":[{"id":"HP:0002179","label":"Opisthotonus"}]}},{"entity":"ClinVarVariant:24621","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:201582","phenotype":{"types":[{"id":"HP:0100749","label":"Chest pain"}]}},{"entity":"ClinVarVariant:38322","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"MGI:1856691","phenotype":{"types":[{"id":"MP:0011101","label":"prenatal lethality, incomplete penetrance"}]}},{"entity":"ClinVarVariant:12207","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"ClinVarVariant:5028","phenotype":{"types":[{"id":"HP:0000230","label":"Gingivitis"}]}},{"entity":"MGI:3574072","phenotype":{"types":[{"id":"GO:0014037PHENOTYPE","label":"Schwann cell differentiation phenotype"}]}},{"entity":"FlyBase:FBal0206015","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:52308","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:53376","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:135892","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"AQTL:9532","phenotype":{"types":[{"id":"AQTLTrait:2029","label":"Tibia bone mineral content"}]}},{"entity":"ClinVarVariant:82771","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"ClinVarVariant:53264","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"FlyBase:FBal0218574","phenotype":{"types":[{"id":"FBbt:00004889PHENOTYPE","label":"karyosome phenotype"}]}},{"entity":"ClinVarVariant:35967","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"dbSNP:rs17135859","phenotype":{"types":[{"id":"HP:0002140","label":"Ischemic stroke"}]}},{"entity":"ClinVarVariant:159941","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"MGI:2181294","phenotype":{"types":[{"id":"MP:0009409","label":"abnormal skeletal muscle fiber type ratio"}]}},{"entity":"ClinVarVariant:211646","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"MGI:5056148","phenotype":{"types":[{"id":"MP:0001923","label":"reduced female fertility"}]}},{"entity":"ClinVarVariant:6711","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:163766","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ZFIN:ZDB-ALT-091112-20","phenotype":{"types":[{"id":"ZP:0001833","label":"abnormal(ly) deformed cranial cartilage"}]}},{"entity":"ClinVarVariant:39297","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"MGI:5441069","phenotype":{"types":[{"id":"MP:0004046","label":"abnormal mitosis"}]}},{"entity":"ClinVarVariant:24468","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:216732","phenotype":{"types":[{"id":"HP:0001541","label":"Ascites"}]}},{"entity":"FlyBase:FBal0316487","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"MGI:2183949","phenotype":{"types":[{"id":"MP:0003786","label":"premature aging"}]}},{"entity":"ClinVarVariant:41161","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:36567","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:24386","phenotype":{"types":[{"id":"HP:0008063","label":"Aplasia/Hypoplasia of the lens"}]}},{"entity":"AQTL:10182","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:158363","phenotype":{"types":[{"id":"HP:0000742","label":"Self-mutilation"}]}},{"entity":"ClinVarVariant:100721","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"MGI:3664305","phenotype":{"types":[{"id":"MP:0003137","label":"abnormal impulse conducting system conduction"}]}},{"entity":"ClinVarVariant:17282","phenotype":{"types":[{"id":"HP:0002273","label":"Tetraparesis"}]}},{"entity":"ClinVarVariant:159049","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:21789","phenotype":{"types":[{"id":"HP:0002411","label":"Myokymia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004726-WBRNAi00008634","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:4531","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:36309","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"ClinVarVariant:4367","phenotype":{"types":[{"id":"HP:0001776","label":"Bilateral talipes equinovarus"}]}},{"entity":"ClinVarVariant:67986","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:41142","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-030616-579-ZDB-MRPHLNO-070531-6","phenotype":{"types":[{"id":"GO:0031016PHENOTYPE","label":"pancreas development phenotype"}]}},{"entity":"ClinVarVariant:31224","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:199204","phenotype":{"types":[{"id":"HP:0002153","label":"Hyperkalemia"}]}},{"entity":"ClinVarVariant:13419","phenotype":{"types":[{"id":"HP:0002315","label":"Headache"}]}},{"entity":"ClinVarVariant:64785","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:198957","phenotype":{"types":[{"id":"HP:0010454","label":"Acetabular spurs"}]}},{"entity":"ClinVarVariant:6542","phenotype":{"types":[{"id":"HP:0007476","label":"Anhidrotic ectodermal dysplasia"}]}},{"entity":"ClinVarVariant:2648","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"FlyBase:FBal0051173","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:10766","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"AQTL:8854","phenotype":{"types":[{"id":"AQTLTrait:491","label":"Ear size"}]}},{"entity":"ClinVarVariant:136109","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:29986","phenotype":{"types":[{"id":"HP:0001376","label":"Limitation of joint mobility"}]}},{"entity":"ClinVarVariant:211645","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"ClinVarVariant:158349","phenotype":{"types":[{"id":"HP:0000343","label":"Long philtrum"}]}},{"entity":"ClinVarVariant:134889","phenotype":{"types":[{"id":"HP:0100634","label":"Neuroendocrine neoplasm"}]}},{"entity":"ClinVarVariant:10738","phenotype":{"types":[{"id":"HP:0100699","label":"Scarring"}]}},{"entity":"FlyBase:FBal0209081","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:190276","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"ClinVarVariant:14271","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:204288","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:155948","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:48922","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"ClinVarVariant:83179","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"ClinVarVariant:30382","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:204092","phenotype":{"types":[{"id":"HP:0009830","label":"Peripheral neuropathy"}]}},{"entity":"ClinVarVariant:13714","phenotype":{"types":[{"id":"HP:0002155","label":"Hypertriglyceridemia"}]}},{"entity":"ClinVarVariant:10130","phenotype":{"types":[{"id":"HP:0001410","label":"Decreased liver function"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022792-WBRNAi00100525","phenotype":{"types":[{"id":"WBPhenotype:0000154","label":"reduced brood size"}]}},{"entity":"ClinVarVariant:38788","phenotype":{"types":[{"id":"HP:0011507","label":"Macular flecks"}]}},{"entity":"ClinVarVariant:16636","phenotype":{"types":[{"id":"HP:0007110","label":"Central hypoventilation"}]}},{"entity":"ClinVarVariant:215714","phenotype":{"types":[{"id":"HP:0002076","label":"Migraine"}]}},{"entity":"ClinVarVariant:92913","phenotype":{"types":[{"id":"HP:0100670","label":"Rough bone trabeculation"}]}},{"entity":"ClinVarVariant:142700","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:161996","phenotype":{"types":[{"id":"HP:0006538","label":"Recurrent bronchopulmonary infections"}]}},{"entity":"ClinVarVariant:162456","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:195849","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"AQTL:27763","phenotype":{"types":[{"id":"AQTLTrait:1485","label":"Mean corpuscular volume"}]}},{"entity":"ClinVarVariant:41168","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"AQTL:44243","phenotype":{"types":[{"id":"AQTLTrait:1136","label":"Bone quality"}]}},{"entity":"MGI:3772332","phenotype":{"types":[{"id":"MP:0000490","label":"abnormal crypts of Lieberkuhn morphology"}]}},{"entity":"ClinVarVariant:38414","phenotype":{"types":[{"id":"HP:0100790","label":"Hernia"}]}},{"entity":"ClinVarVariant:48957","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:65312","phenotype":{"types":[{"id":"HP:0000826","label":"Precocious puberty"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-060908-2-ZDB-MRPHLNO-100616-1","phenotype":{"types":[{"id":"ZP:0001349","label":"abnormal(ly) apoptotic eye"}]}},{"entity":"ClinVarVariant:5595","phenotype":{"types":[{"id":"HP:0002013","label":"Vomiting"}]}},{"entity":"AQTL:32791","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:160181","phenotype":{"types":[{"id":"HP:0001321","label":"Cerebellar hypoplasia"}]}},{"entity":"AQTL:53986","phenotype":{"types":[{"id":"AQTLTrait:1153","label":"Stillbirth"}]}},{"entity":"ClinVarVariant:10733","phenotype":{"types":[{"id":"HP:0001633","label":"Abnormality of the mitral valve"}]}},{"entity":"ClinVarVariant:49640","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:217079","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:97787","phenotype":{"types":[{"id":"HP:0100603","label":"Toxemia of pregnancy"}]}},{"entity":"ClinVarVariant:97554","phenotype":{"types":[{"id":"HP:0100769","label":"Synovitis"}]}},{"entity":"ClinVarVariant:11060","phenotype":{"types":[{"id":"HP:0002021","label":"Pyloric stenosis"}]}},{"entity":"ClinVarVariant:53357","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"ClinVarVariant:210443","phenotype":{"types":[{"id":"HP:0100545","label":"Arterial stenosis"}]}},{"entity":"MGI:4453204","phenotype":{"types":[{"id":"MP:0001922","label":"reduced male fertility"}]}},{"entity":"ClinVarVariant:35833","phenotype":{"types":[{"id":"HP:0001742","label":"Nasal obstruction"}]}},{"entity":"MGI:1856066","phenotype":{"types":[{"id":"HP:0011096","label":"Peripheral demyelination"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004919-WBRNAi00071373","phenotype":{"types":[{"id":"WBPhenotype:0000258","label":"cell secretion variant"}]}},{"entity":"ClinVarVariant:38626","phenotype":{"types":[{"id":"HP:0001578","label":"Hypercortisolism"}]}},{"entity":"ClinVarVariant:31676","phenotype":{"types":[{"id":"HP:0000448","label":"Prominent nose"}]}},{"entity":"MGI:3614434","phenotype":{"types":[{"id":"MP:0005536","label":"Leydig cell hypoplasia"}]}},{"entity":"ClinVarVariant:21358","phenotype":{"types":[{"id":"HP:0002553","label":"Highly arched eyebrow"}]}},{"entity":"ClinVarVariant:126095","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:3382","phenotype":{"types":[{"id":"HP:0006485","label":"Agenesis of incisor"}]}},{"entity":"ClinVarVariant:185554","phenotype":{"types":[{"id":"HP:0006721","label":"Acute lymphoblastic leukemia"}]}},{"entity":"FlyBase:FBal0135765","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"AQTL:6504","phenotype":{"types":[{"id":"AQTLTrait:2021","label":"Humerus length"}]}},{"entity":"ClinVarVariant:42385","phenotype":{"types":[{"id":"HP:0100719","label":"Lens coloboma"}]}},{"entity":"ClinVarVariant:53360","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:127117","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:25201","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"ClinVarVariant:189862","phenotype":{"types":[{"id":"HP:0002384","label":"Focal seizures with impairment of consciousness or awareness"}]}},{"entity":"ClinVarVariant:183683","phenotype":{"types":[{"id":"HP:0003164","label":"Hypothalamic gonadotropin-releasing hormone (GNRH) deficiency"}]}},{"entity":"ClinVarVariant:159370","phenotype":{"types":[{"id":"HP:0009890","label":"High anterior hairline"}]}},{"entity":"ClinVarVariant:216775","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"MGI:4364913","phenotype":{"types":[{"id":"MP:0006411","label":"upturned snout"}]}},{"entity":"MGI:1857852","phenotype":{"types":[{"id":"MP:0000872","label":"abnormal cerebellum external granule cell layer morphology"}]}},{"entity":"ClinVarVariant:215957","phenotype":{"types":[{"id":"HP:0005344","label":"Abnormality of the carotid arteries"}]}},{"entity":"MGI:3777145","phenotype":{"types":[{"id":"MP:0001981","label":"increased chemically-elicited antinociception"}]}},{"entity":"ClinVarVariant:65753","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:56716","phenotype":{"types":[{"id":"HP:0002074","label":"Increased neuronal autofluorescent lipopigment"}]}},{"entity":"ClinVarVariant:6643","phenotype":{"types":[{"id":"HP:0004944","label":"Cerebral aneurysm"}]}},{"entity":"ClinVarVariant:143406","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003920-WBRNAi00069781","phenotype":{"types":[{"id":"WBPhenotype:0000061","label":"extended life span"}]}},{"entity":"ClinVarVariant:7623","phenotype":{"types":[{"id":"HP:0001297","label":"Stroke"}]}},{"entity":"ZFIN:ZDB-ALT-040824-2","phenotype":{"types":[{"id":"ZP:0000961","label":"abnormal(ly) bent trunk"}]}},{"entity":"ClinVarVariant:35839","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:158283","phenotype":{"types":[{"id":"HP:0001888","label":"Lymphopenia"}]}},{"entity":"AQTL:31062","phenotype":{"types":[{"id":"AQTLTrait:1169","label":"Interval to first estrus after calving"}]}},{"entity":"ClinVarVariant:11454","phenotype":{"types":[{"id":"HP:0000971","label":"Abnormality of the sweat gland"}]}},{"entity":"ClinVarVariant:17349","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"MGI:1927183","phenotype":{"types":[{"id":"MP:0008571","label":"abnormal synaptic bouton morphology"}]}},{"entity":"ClinVarVariant:211736","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:54175","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:132825","phenotype":{"types":[{"id":"HP:0002140","label":"Ischemic stroke"}]}},{"entity":"MGI:3620102","phenotype":{"types":[{"id":"MP:0003887","label":"increased hepatocyte apoptosis"}]}},{"entity":"MGI:2450309","phenotype":{"types":[{"id":"MP:0000260","label":"abnormal angiogenesis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001691-WBRNAi00076971","phenotype":{"types":[{"id":"WBPhenotype:0000280","label":"breaks in alae"}]}},{"entity":"ClinVarVariant:97923","phenotype":{"types":[{"id":"HP:0001917","label":"Renal amyloidosis"}]}},{"entity":"FlyBase:FBal0138238","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:88857","phenotype":{"types":[{"id":"HP:0000787","label":"Nephrolithiasis"}]}},{"entity":"ClinVarVariant:788","phenotype":{"types":[{"id":"HP:0001640","label":"Cardiomegaly"}]}},{"entity":"ClinVarVariant:11901","phenotype":{"types":[{"id":"HP:0008169","label":"Reduced factor VII activity"}]}},{"entity":"MGI:2388055","phenotype":{"types":[{"id":"MP:0005325","label":"abnormal renal glomerulus morphology"}]}},{"entity":"ClinVarVariant:30944","phenotype":{"types":[{"id":"HP:0003026","label":"Short long bone"}]}},{"entity":"ClinVarVariant:1483","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:1369","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:41065","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:10108","phenotype":{"types":[{"id":"HP:0100726","label":"Kaposi's sarcoma"}]}},{"entity":"ClinVarVariant:10757","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"ClinVarVariant:210471","phenotype":{"types":[{"id":"HP:0002208","label":"Coarse hair"}]}},{"entity":"AQTL:12523","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"dbSNP:rs12294076","phenotype":{"types":[{"id":"HP:0000211","label":"Trismus"}]}},{"entity":"ClinVarVariant:4221","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:159447","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"MGI:4432654","phenotype":{"types":[{"id":"MP:0003131","label":"increased erythrocyte cell number"}]}},{"entity":"ClinVarVariant:216216","phenotype":{"types":[{"id":"HP:0003254","label":"Abnormality of DNA repair"}]}},{"entity":"ClinVarVariant:42397","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"MGI:1933764","phenotype":{"types":[{"id":"MP:0000814","label":"absent dentate gyrus"}]}},{"entity":"ClinVarVariant:5487","phenotype":{"types":[{"id":"HP:0011958","label":"Retinal perforation"}]}},{"entity":"ClinVarVariant:158894","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:10987","phenotype":{"types":[{"id":"HP:0003217","label":"Hyperglutaminemia"}]}},{"entity":"ClinVarVariant:53294","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:10124","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:30491","phenotype":{"types":[{"id":"HP:0003765","label":"Psoriasis"}]}},{"entity":"ClinVarVariant:189593","phenotype":{"types":[{"id":"HP:0002360","label":"Sleep disturbance"}]}},{"entity":"ClinVarVariant:68497","phenotype":{"types":[{"id":"HP:0001047","label":"Atopic dermatitis"}]}},{"entity":"ClinVarVariant:210028","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:9922","phenotype":{"types":[{"id":"HP:0010529","label":"Echolalia"}]}},{"entity":"ClinVarVariant:42017","phenotype":{"types":[{"id":"HP:0000951","label":"Abnormality of the skin"}]}},{"entity":"ClinVarVariant:35887","phenotype":{"types":[{"id":"HP:0002113","label":"Pulmonary infiltrates"}]}},{"entity":"ClinVarVariant:143254","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"ZFIN:ZDB-ALT-121210-2","phenotype":{"types":[{"id":"ZP:0012714","label":"abnormal(ly) mislocalised pancreas neutrophil"}]}},{"entity":"ClinVarVariant:53973","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:99926","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:39637","phenotype":{"types":[{"id":"HP:0000405","label":"Conductive hearing impairment"}]}},{"entity":"ClinVarVariant:30547","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ClinVarVariant:36051","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:11592","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"ClinVarVariant:4301","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:42066","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:41149","phenotype":{"types":[{"id":"HP:0000668","label":"Hypodontia"}]}},{"entity":"MGI:1856601","phenotype":{"types":[{"id":"MP:0009474","label":"thick epidermis stratum spinosum"}]}},{"entity":"ClinVarVariant:38306","phenotype":{"types":[{"id":"HP:0008551","label":"Microtia"}]}},{"entity":"ClinVarVariant:1957","phenotype":{"types":[{"id":"HP:0002644","label":"Abnormality of pelvic girdle bone morphology"}]}},{"entity":"ClinVarVariant:24677","phenotype":{"types":[{"id":"HP:0100633","label":"Esophagitis"}]}},{"entity":"ClinVarVariant:179546","phenotype":{"types":[{"id":"HP:0002017","label":"Nausea and vomiting"}]}},{"entity":"ClinVarVariant:189086","phenotype":{"types":[{"id":"HP:0000400","label":"Macrotia"}]}},{"entity":"ClinVarVariant:1450","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"MGI:5513765","phenotype":{"types":[{"id":"MP:0005635","label":"decreased circulating bilirubin level"}]}},{"entity":"ClinVarVariant:53628","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:126974","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:199200","phenotype":{"types":[{"id":"HP:0012043","label":"Pendular nystagmus"}]}},{"entity":"ClinVarVariant:53703","phenotype":{"types":[{"id":"HP:0100660","label":"Dyskinesia"}]}},{"entity":"MGI:3695897","phenotype":{"types":[{"id":"MP:0000755","label":"hindlimb paralysis"}]}},{"entity":"MGI:3040330","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"ClinVarVariant:7165","phenotype":{"types":[{"id":"HP:0001081","label":"Cholelithiasis"}]}},{"entity":"ClinVarVariant:5894","phenotype":{"types":[{"id":"HP:0000509","label":"Conjunctivitis"}]}},{"entity":"AQTL:26651","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:9617","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"FlyBase:FBal0261159","phenotype":{"types":[{"id":"FBcv:0000399","label":"courtship behavior defective"}]}},{"entity":"ClinVarVariant:159204","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:211653","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"MGI:2677447","phenotype":{"types":[{"id":"MP:0001825","label":"arrested T cell differentiation"}]}},{"entity":"ClinVarVariant:210388","phenotype":{"types":[{"id":"HP:0005054","label":"Metaphyseal spurs"}]}},{"entity":"ClinVarVariant:49421","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"ClinVarVariant:6459","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:5082","phenotype":{"types":[{"id":"HP:0003557","label":"Increased variability in muscle fiber diameter"}]}},{"entity":"ClinVarVariant:6582","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"ClinVarVariant:8884","phenotype":{"types":[{"id":"HP:0000567","label":"Chorioretinal coloboma"}]}},{"entity":"MGI:2179545","phenotype":{"types":[{"id":"MP:0002123","label":"abnormal definitive hematopoiesis"}]}},{"entity":"ClinVarVariant:53369","phenotype":{"types":[{"id":"HP:0000855","label":"Insulin resistance"}]}},{"entity":"MGI:2180680","phenotype":{"types":[{"id":"MP:0008188","label":"abnormal transitional stage B cell morphology"}]}},{"entity":"FlyBase:FBal0304813","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:49575","phenotype":{"types":[{"id":"HP:0009716","label":"Subependymal nodules"}]}},{"entity":"ClinVarVariant:1018","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:48862","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"MGI:2662305","phenotype":{"types":[{"id":"MP:0001622","label":"abnormal vasculogenesis"}]}},{"entity":"ClinVarVariant:39056","phenotype":{"types":[{"id":"HP:0003026","label":"Short long bone"}]}},{"entity":"ClinVarVariant:10743","phenotype":{"types":[{"id":"HP:0009763","label":"Limb pain"}]}},{"entity":"ClinVarVariant:44203","phenotype":{"types":[{"id":"HP:0007411","label":"Hypoplastic-absent sebaceous glands"}]}},{"entity":"MGI:1857291","phenotype":{"types":[{"id":"MP:0000628","label":"abnormal mammary gland development"}]}},{"entity":"ClinVarVariant:158724","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"MGI:2149065","phenotype":{"types":[{"id":"MP:0001900","label":"impaired synaptic plasticity"}]}},{"entity":"ClinVarVariant:97611","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"MGI:2176201","phenotype":{"types":[{"id":"MP:0003566","label":"abnormal cell adhesion"}]}},{"entity":"ClinVarVariant:24806","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ClinVarVariant:158359","phenotype":{"types":[{"id":"HP:0009765","label":"Low hanging columella"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003918-WBRNAi00083243","phenotype":{"types":[{"id":"WBPhenotype:0000425","label":"antibody staining reduced"}]}},{"entity":"ClinVarVariant:68536","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"FlyBase:FBal0059988","phenotype":{"types":[{"id":"FBbt:00004218PHENOTYPE","label":"Drosophila rhabdomere R3 phenotype"}]}},{"entity":"ClinVarVariant:53220","phenotype":{"types":[{"id":"HP:0006536","label":"Obstructive lung disease"}]}},{"entity":"ClinVarVariant:11550","phenotype":{"types":[{"id":"HP:0002747","label":"Respiratory insufficiency due to muscle weakness"}]}},{"entity":"WormBase:WBVar00252908","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:156338","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:31196","phenotype":{"types":[{"id":"HP:0003128","label":"Lactic acidosis"}]}},{"entity":"ClinVarVariant:10709","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"ClinVarVariant:65353","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:38749","phenotype":{"types":[{"id":"HP:0005101","label":"High-frequency hearing impairment"}]}},{"entity":"ClinVarVariant:53801","phenotype":{"types":[{"id":"HP:0006538","label":"Recurrent bronchopulmonary infections"}]}},{"entity":"ClinVarVariant:5561","phenotype":{"types":[{"id":"HP:0005227","label":"Adenomatous colonic polyposis"}]}},{"entity":"ClinVarVariant:136110","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:156138","phenotype":{"types":[{"id":"HP:0001319","label":"Neonatal hypotonia"}]}},{"entity":"ClinVarVariant:120246","phenotype":{"types":[{"id":"HP:0002162","label":"Low posterior hairline"}]}},{"entity":"ClinVarVariant:196277","phenotype":{"types":[{"id":"HP:0006510","label":"Chronic obstructive pulmonary disease"}]}},{"entity":"FlyBase:FBal0207442","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"dbSNP:rs41946434","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"MGI:2176172","phenotype":{"types":[{"id":"MP:0000876","label":"Purkinje cell degeneration"}]}},{"entity":"dbSNP:rs43488797","phenotype":{"types":[{"id":"AQTLTrait:1120","label":"Thurl width"}]}},{"entity":"ClinVarVariant:65533","phenotype":{"types":[{"id":"HP:0004432","label":"Agammaglobulinemia"}]}},{"entity":"ClinVarVariant:7706","phenotype":{"types":[{"id":"HP:0000114","label":"Proximal tubulopathy"}]}},{"entity":"ClinVarVariant:135896","phenotype":{"types":[{"id":"HP:0009733","label":"Glioma"}]}},{"entity":"ClinVarVariant:38975","phenotype":{"types":[{"id":"HP:0003236","label":"Elevated serum creatine phosphokinase"}]}},{"entity":"ClinVarVariant:1967","phenotype":{"types":[{"id":"HP:0002644","label":"Abnormality of pelvic girdle bone morphology"}]}},{"entity":"ClinVarVariant:127165","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:189084","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:1173","phenotype":{"types":[{"id":"HP:0008726","label":"Hypoplasia of the vagina"}]}},{"entity":"ClinVarVariant:15413","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"dbSNP:rs81307772","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"NCBIGene:100462676","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"AQTL:44219","phenotype":{"types":[{"id":"AQTLTrait:1173","label":"Rear leg set"}]}},{"entity":"FlyBase:FBal0284419","phenotype":{"types":[{"id":"FBbt:00003625PHENOTYPE","label":"Drosophila adult brain cell body rind phenotype"}]}},{"entity":"dbSNP:rs110474527","phenotype":{"types":[{"id":"AQTLTrait:1070","label":"Inseminations per conception"}]}},{"entity":"ClinVarVariant:13325","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:156338","phenotype":{"types":[{"id":"HP:0002863","label":"Myelodysplasia"}]}},{"entity":"ClinVarVariant:53718","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:208015","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"FlyBase:FBal0201465","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:41102","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:101364","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:35456","phenotype":{"types":[{"id":"HP:0002097","label":"Emphysema"}]}},{"entity":"WormBase:WBVar00087959","phenotype":{"types":[{"id":"WBPhenotype:0001645","label":"protein degradation variant"}]}},{"entity":"ClinVarVariant:120266","phenotype":{"types":[{"id":"HP:0001010","label":"Hypopigmentation of the skin"}]}},{"entity":"FlyBase:FBal0210406","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:10315","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:53332","phenotype":{"types":[{"id":"HP:0100889","label":"Abnormality of the ductus choledochus"}]}},{"entity":"ClinVarVariant:210467","phenotype":{"types":[{"id":"HP:0008070","label":"Sparse hair"}]}},{"entity":"ClinVarVariant:101212","phenotype":{"types":[{"id":"HP:0005267","label":"Premature delivery because of cervical insufficiency or membrane fragility"}]}},{"entity":"ClinVarVariant:24816","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ZFIN:ZDB-ALT-040716-2","phenotype":{"types":[{"id":"ZP:0006289","label":"abnormal(ly) detached from goblet cell towards intestinal epithelium"}]}},{"entity":"ClinVarVariant:65876","phenotype":{"types":[{"id":"HP:0009824","label":"Upper limb undergrowth"}]}},{"entity":"ClinVarVariant:24437","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"FlyBase:FBal0182631","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:53907","phenotype":{"types":[{"id":"HP:0005232","label":"Pancreatic dysplasia"}]}},{"entity":"FlyBase:FBal0211026","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:92734","phenotype":{"types":[{"id":"HP:0100324","label":"Scleroderma"}]}},{"entity":"ClinVarVariant:209982","phenotype":{"types":[{"id":"HP:0003487","label":"Babinski sign"}]}},{"entity":"ClinVarVariant:126869","phenotype":{"types":[{"id":"HP:0004724","label":"Calcium nephrolithiasis"}]}},{"entity":"ClinVarVariant:101374","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:42515","phenotype":{"types":[{"id":"HP:0000859","label":"Hyperaldosteronism"}]}},{"entity":"ClinVarVariant:188150","phenotype":{"types":[{"id":"HP:0009650","label":"Short distal phalanx of the thumb"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00044068-WBRNAi00075201","phenotype":{"types":[{"id":"WBPhenotype:0000154","label":"reduced brood size"}]}},{"entity":"ClinVarVariant:10457","phenotype":{"types":[{"id":"HP:0007763","label":"Retinal telangiectasia"}]}},{"entity":"ZFIN:ZDB-ALT-151110-1","phenotype":{"types":[{"id":"ZP:0002010","label":"abnormal(ly) morphology pancreas"}]}},{"entity":"FlyBase:FBal0208456","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:97422","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:7963","phenotype":{"types":[{"id":"HP:0010808","label":"Protruding tongue"}]}},{"entity":"ClinVarVariant:159677","phenotype":{"types":[{"id":"HP:0000368","label":"Low-set, posteriorly rotated ears"}]}},{"entity":"ClinVarVariant:21275","phenotype":{"types":[{"id":"HP:0011069","label":"Increased number of teeth"}]}},{"entity":"ClinVarVariant:39124","phenotype":{"types":[{"id":"HP:0006510","label":"Chronic obstructive pulmonary disease"}]}},{"entity":"ClinVarVariant:24454","phenotype":{"types":[{"id":"HP:0007763","label":"Retinal telangiectasia"}]}},{"entity":"MGI:3513254","phenotype":{"types":[{"id":"GO:0001756PHENOTYPE","label":"somitogenesis phenotype"}]}},{"entity":"ClinVarVariant:208427","phenotype":{"types":[{"id":"HP:0000926","label":"Platyspondyly"}]}},{"entity":"ClinVarVariant:3365","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:160227","phenotype":{"types":[{"id":"HP:0002070","label":"Limb ataxia"}]}},{"entity":"ClinVarVariant:53941","phenotype":{"types":[{"id":"HP:0003453","label":"Antineutrophil antibody positivity"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003020-WBRNAi00075368","phenotype":{"types":[{"id":"WBPhenotype:0000700","label":"multivulva"}]}},{"entity":"ClinVarVariant:161234","phenotype":{"types":[{"id":"HP:0007906","label":"Increased intraocular pressure"}]}},{"entity":"ClinVarVariant:217039","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"AQTL:23159","phenotype":{"types":[{"id":"AQTLTrait:2061","label":"Wing weight"}]}},{"entity":"MGI:3716711","phenotype":{"types":[{"id":"HP:0040189","label":"Scaling skin"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001832-WBRNAi00005000","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"WormBase:WBVar00087794","phenotype":{"types":[{"id":"WBPhenotype:0001683","label":"spermatogenesis defective hermaphrodite"}]}},{"entity":"AQTL:17561","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:11816","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:35572","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:211143","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"MGI:2180013","phenotype":{"types":[{"id":"MP:0001119","label":"abnormal female reproductive system morphology"}]}},{"entity":"FlyBase:FBal0296773","phenotype":{"types":[{"id":"FBbt:00004729PHENOTYPE","label":"Drosophila wing phenotype"}]}},{"entity":"ClinVarVariant:54008","phenotype":{"types":[{"id":"HP:0011850","label":"Parotitis"}]}},{"entity":"ClinVarVariant:183671","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"MGI:3615021","phenotype":{"types":[{"id":"HP:0004447","label":"Poikilocytosis"}]}},{"entity":"ClinVarVariant:18370","phenotype":{"types":[{"id":"HP:0000343","label":"Long philtrum"}]}},{"entity":"MGI:2429312","phenotype":{"types":[{"id":"MP:0006404","label":"abnormal lumbar dorsal root ganglion morphology"}]}},{"entity":"ClinVarVariant:10859","phenotype":{"types":[{"id":"HP:0010299","label":"Abnormality of dentin"}]}},{"entity":"ClinVarVariant:101185","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:3866","phenotype":{"types":[{"id":"HP:0002275","label":"Poor motor coordination"}]}},{"entity":"ClinVarVariant:42377","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"ClinVarVariant:55944","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:10728","phenotype":{"types":[{"id":"HP:0000763","label":"Sensory neuropathy"}]}},{"entity":"dbSNP:rs109894613","phenotype":{"types":[{"id":"AQTLTrait:1115","label":"Chest width"}]}},{"entity":"ClinVarVariant:92621","phenotype":{"types":[{"id":"HP:0003541","label":"Urinary glycosaminoglycan excretion"}]}},{"entity":"ClinVarVariant:31028","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"ZFIN:ZDB-ALT-090702-3","phenotype":{"types":[{"id":"ZP:0015766","label":"abnormal(ly) black mouth melanoma"}]}},{"entity":"ClinVarVariant:11734","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"FlyBase:FBal0194748","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:100637","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:135758","phenotype":{"types":[{"id":"HP:0008348","label":"Immunoglobulin IgG2 deficiency"}]}},{"entity":"ClinVarVariant:38922","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:10582","phenotype":{"types":[{"id":"HP:0005186","label":"Synovial hypertrophy"}]}},{"entity":"ClinVarVariant:216388","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:24677","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"MGI:3665249","phenotype":{"types":[{"id":"MP:0013744","label":"abnormal conjunctival sac morphology"}]}},{"entity":"ClinVarVariant:2715","phenotype":{"types":[{"id":"HP:0000992","label":"Cutaneous photosensitivity"}]}},{"entity":"ClinVarVariant:25244","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:161456","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:7165","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:10229","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:216144","phenotype":{"types":[{"id":"HP:0000090","label":"Nephronophthisis"}]}},{"entity":"MGI:3837303","phenotype":{"types":[{"id":"HP:0011116","label":"Abnormality of interferon secretion"}]}},{"entity":"ClinVarVariant:1460","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:56659","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004357-WBRNAi00085604","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:24792","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:135759","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"MGI:2682796","phenotype":{"types":[{"id":"MP:0003156","label":"abnormal leukocyte migration"}]}},{"entity":"ClinVarVariant:5946","phenotype":{"types":[{"id":"HP:0001260","label":"Dysarthria"}]}},{"entity":"ClinVarVariant:159201","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:49536","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:7401","phenotype":{"types":[{"id":"HP:0001100","label":"Heterochromia iridis"}]}},{"entity":"FlyBase:FBal0264413","phenotype":{"types":[{"id":"FBbt:00001896PHENOTYPE","label":"Drosophila embryonic/larval Malpighian tubule phenotype"}]}},{"entity":"ClinVarVariant:1049","phenotype":{"types":[{"id":"HP:0000682","label":"Abnormality of dental enamel"}]}},{"entity":"ClinVarVariant:67861","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"MGI:4288793","phenotype":{"types":[{"id":"HP:0000137","label":"Abnormality of the ovary"}]}},{"entity":"FlyBase:FBal0199496","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:53723","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"FlyBase:FBal0209583","phenotype":{"types":[{"id":"FBbt:00004580PHENOTYPE","label":"Drosophila mesothoracic tergum phenotype"}]}},{"entity":"ClinVarVariant:44810","phenotype":{"types":[{"id":"HP:0000465","label":"Webbed neck"}]}},{"entity":"ClinVarVariant:15485","phenotype":{"types":[{"id":"HP:0000786","label":"Primary amenorrhea"}]}},{"entity":"ClinVarVariant:216565","phenotype":{"types":[{"id":"HP:0005403","label":"T lymphocytopenia"}]}},{"entity":"ClinVarVariant:91690","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:92324","phenotype":{"types":[{"id":"HP:0000726","label":"Dementia"}]}},{"entity":"ClinVarVariant:24458","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"dbSNP:rs1075309","phenotype":{"types":[{"id":"HP:0011134","label":"Low-grade fever"}]}},{"entity":"ClinVarVariant:165011","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:8836","phenotype":{"types":[{"id":"HP:0011036","label":"Abnormality of renal excretion"}]}},{"entity":"ClinVarVariant:96439","phenotype":{"types":[{"id":"HP:0000457","label":"Depressed nasal ridge"}]}},{"entity":"ClinVarVariant:210712","phenotype":{"types":[{"id":"HP:0008572","label":"External ear malformation"}]}},{"entity":"ClinVarVariant:187907","phenotype":{"types":[{"id":"HP:0100786","label":"Hypersomnia"}]}},{"entity":"ClinVarVariant:53514","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"ClinVarVariant:159161","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"FlyBase:FBal0230433","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:35716","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:16678","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:10731","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:53667","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:211663","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"ClinVarVariant:5779","phenotype":{"types":[{"id":"HP:0000722","label":"Obsessive-compulsive behavior"}]}},{"entity":"ClinVarVariant:97644","phenotype":{"types":[{"id":"HP:0100539","label":"Periorbital edema"}]}},{"entity":"ClinVarVariant:159206","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:53393","phenotype":{"types":[{"id":"HP:0006706","label":"Cystic liver disease"}]}},{"entity":"ClinVarVariant:83176","phenotype":{"types":[{"id":"HP:0006740","label":"Transitional cell carcinoma of the bladder"}]}},{"entity":"ClinVarVariant:48917","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:216392","phenotype":{"types":[{"id":"HP:0001012","label":"Multiple lipomas"}]}},{"entity":"ClinVarVariant:161976","phenotype":{"types":[{"id":"HP:0001269","label":"Hemiparesis"}]}},{"entity":"ClinVarVariant:16993","phenotype":{"types":[{"id":"HP:0000691","label":"Microdontia"}]}},{"entity":"FlyBase:FBal0059537","phenotype":{"types":[{"id":"FBbt:00001730PHENOTYPE","label":"Drosophila larval head phenotype"}]}},{"entity":"ClinVarVariant:36475","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:159214","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:7155","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:11662","phenotype":{"types":[{"id":"HP:0000687","label":"Widely spaced teeth"}]}},{"entity":"ClinVarVariant:12002","phenotype":{"types":[{"id":"HP:0010980","label":"Hyperlipoproteinemia"}]}},{"entity":"NCBIGene:1913","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"ZFIN:ZDB-ALT-100409-2","phenotype":{"types":[{"id":"ZP:0016420","label":"abnormal(ly) has extra parts of type integument towards cell"}]}},{"entity":"ClinVarVariant:53894","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:167228","phenotype":{"types":[{"id":"HP:0000592","label":"Blue sclerae"}]}},{"entity":"ClinVarVariant:9429","phenotype":{"types":[{"id":"HP:0000632","label":"Lacrimation abnormality"}]}},{"entity":"dbSNP:rs6676375","phenotype":{"types":[{"id":"HP:0001254","label":"Lethargy"}]}},{"entity":"ClinVarVariant:100787","phenotype":{"types":[{"id":"HP:0009803","label":"Short phalanx of finger"}]}},{"entity":"ClinVarVariant:41422","phenotype":{"types":[{"id":"HP:0005855","label":"Multiple prenatal fractures"}]}},{"entity":"ZFIN:ZDB-ALT-070531-2","phenotype":{"types":[{"id":"ZP:0008366","label":"abnormal(ly) having decreased processual parts liver development towards cell proliferation"}]}},{"entity":"ClinVarVariant:97671","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"MGI:3814908","phenotype":{"types":[{"id":"HP:0010976","label":"B lymphocytopenia"}]}},{"entity":"ClinVarVariant:183069","phenotype":{"types":[{"id":"HP:0008256","label":"Adrenocortical adenoma"}]}},{"entity":"ClinVarVariant:56778","phenotype":{"types":[{"id":"HP:0002084","label":"Encephalocele"}]}},{"entity":"dbSNP:rs41697837","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:2588","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:184381","phenotype":{"types":[{"id":"HP:0002897","label":"Parathyroid adenoma"}]}},{"entity":"ClinVarVariant:135896","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"MGI:1857077","phenotype":{"types":[{"id":"MP:0013173","label":"trigeminal ganglion degeneration"}]}},{"entity":"ClinVarVariant:158776","phenotype":{"types":[{"id":"HP:0000826","label":"Precocious puberty"}]}},{"entity":"ClinVarVariant:1704","phenotype":{"types":[{"id":"HP:0003481","label":"Segmental peripheral demyelination/remyelination"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1302","phenotype":{"types":[{"id":"ZP:0000766","label":"abnormal(ly) bent post-vent region"}]}},{"entity":"ClinVarVariant:200395","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:126966","phenotype":{"types":[{"id":"HP:0001402","label":"Hepatocellular carcinoma"}]}},{"entity":"ClinVarVariant:1633","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"FlyBase:FBal0091132","phenotype":{"types":[{"id":"FBcv:0002027","label":"lethal - all die before end of pupal stage"}]}},{"entity":"ClinVarVariant:48892","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"ClinVarVariant:36061","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:5923","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"MGI:3826836","phenotype":{"types":[{"id":"MP:0009431","label":"decreased fetal weight"}]}},{"entity":"dbSNP:rs11886868","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:159683","phenotype":{"types":[{"id":"HP:0006461","label":"Proximal femoral epiphysiolysis"}]}},{"entity":"MGI:3762641","phenotype":{"types":[{"id":"MP:0011089","label":"perinatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:5545","phenotype":{"types":[{"id":"HP:0000972","label":"Palmoplantar hyperkeratosis"}]}},{"entity":"ClinVarVariant:13344","phenotype":{"types":[{"id":"HP:0000506","label":"Telecanthus"}]}},{"entity":"ClinVarVariant:3988","phenotype":{"types":[{"id":"HP:0006829","label":"Severe muscular hypotonia"}]}},{"entity":"ClinVarVariant:143170","phenotype":{"types":[{"id":"HP:0003474","label":"Sensory impairment"}]}},{"entity":"ClinVarVariant:49708","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:64689","phenotype":{"types":[{"id":"HP:0000445","label":"Wide nose"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006528-WBRNAi00085576","phenotype":{"types":[{"id":"WBPhenotype:0001982","label":"cell membrane organization biogenesis variant"}]}},{"entity":"ClinVarVariant:571","phenotype":{"types":[{"id":"HP:0000618","label":"Blindness"}]}},{"entity":"OMIM:226000","phenotype":{"types":[{"id":"HP:0001711","label":"Abnormality of the left ventricle"}]}},{"entity":"ClinVarVariant:209137","phenotype":{"types":[{"id":"HP:0001673","label":"Tachycardia (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:49501","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:7175","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:210451","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"MGI:3800176","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:120276","phenotype":{"types":[{"id":"HP:0001010","label":"Hypopigmentation of the skin"}]}},{"entity":"ClinVarVariant:24361","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"MGI:3527937","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:216466","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000065-WBRNAi00026399","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"AQTL:40844","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:10887","phenotype":{"types":[{"id":"HP:0002872","label":"Apneic episodes precipitated by illness, fatigue, stress"}]}},{"entity":"ClinVarVariant:10737","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001973-WBRNAi00063017","phenotype":{"types":[{"id":"WBPhenotype:0000709","label":"pharyngeal morphology variant"}]}},{"entity":"ClinVarVariant:3360","phenotype":{"types":[{"id":"HP:0009926","label":"Increased lacrimation"}]}},{"entity":"ClinVarVariant:54089","phenotype":{"types":[{"id":"HP:0001622","label":"Premature birth"}]}},{"entity":"FlyBase:FBal0051201","phenotype":{"types":[{"id":"FBbt:00003921PHENOTYPE","label":"optic chiasma phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000415-WBRNAi00097824","phenotype":{"types":[{"id":"WBPhenotype:0000243","label":"engulfment failure by killer cell"}]}},{"entity":"ClinVarVariant:56788","phenotype":{"types":[{"id":"HP:0002084","label":"Encephalocele"}]}},{"entity":"ClinVarVariant:35859","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:68302","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:209028","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"ClinVarVariant:18331","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:50912","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:634","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:53929","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ClinVarVariant:4330","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"ClinVarVariant:17521","phenotype":{"types":[{"id":"HP:0000127","label":"Renal salt wasting"}]}},{"entity":"MGI:3818518","phenotype":{"types":[{"id":"MP:0004179","label":"transmission ratio distortion"}]}},{"entity":"ClinVarVariant:3097","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"ClinVarVariant:14793","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:24745","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:215969","phenotype":{"types":[{"id":"HP:0007707","label":"Congenital primary aphakia"}]}},{"entity":"ClinVarVariant:12401","phenotype":{"types":[{"id":"HP:0002290","label":"Poliosis"}]}},{"entity":"FlyBase:FBal0199313","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"MGI:5086003","phenotype":{"types":[{"id":"MP:0010875","label":"increased bone volume"}]}},{"entity":"MGI:3707421","phenotype":{"types":[{"id":"MP:0003088","label":"abnormal prepulse inhibition"}]}},{"entity":"ClinVarVariant:55954","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:97691","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"NCBIGene:171","phenotype":{"types":[{"id":"HP:0001199","label":"Triphalangeal thumb"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004978-WBRNAi00084613","phenotype":{"types":[{"id":"WBPhenotype:0001719","label":"unfolded protein response variant"}]}},{"entity":"ClinVarVariant:143524","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"ClinVarVariant:3678","phenotype":{"types":[{"id":"HP:0002194","label":"Delayed gross motor development"}]}},{"entity":"FlyBase:FBal0040484","phenotype":{"types":[{"id":"FBbt:00001761PHENOTYPE","label":"Drosophila imaginal disc phenotype"}]}},{"entity":"ClinVarVariant:10176","phenotype":{"types":[{"id":"HP:0005268","label":"Spontaneous abortion"}]}},{"entity":"ClinVarVariant:49511","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:54082","phenotype":{"types":[{"id":"HP:0012236","label":"Elevated sweat chloride"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00021351-WBRNAi00080537","phenotype":{"types":[{"id":"WBPhenotype:0000154","label":"reduced brood size"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002324-WBRNAi00000137","phenotype":{"types":[{"id":"WBPhenotype:0000038","label":"exploded through vulva"}]}},{"entity":"MGI:1926955","phenotype":{"types":[{"id":"HP:0001067","label":"Neurofibromas"}]}},{"entity":"ClinVarVariant:101404","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:180631","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"ClinVarVariant:66441","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"ClinVarVariant:2241","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"FlyBase:FBal0062864","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:1730","phenotype":{"types":[{"id":"HP:0007503","label":"Generalized ichthyosis"}]}},{"entity":"ClinVarVariant:82791","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"ClinVarVariant:30189","phenotype":{"types":[{"id":"HP:0000845","label":"Growth hormone excess"}]}},{"entity":"ClinVarVariant:558","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:6718","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"MGI:2674242","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"MGI:3757609","phenotype":{"types":[{"id":"MP:0003107","label":"abnormal response to novelty"}]}},{"entity":"ClinVarVariant:7394","phenotype":{"types":[{"id":"HP:0002226","label":"White eyebrow"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003048-WBRNAi00062630","phenotype":{"types":[{"id":"WBPhenotype:0001102","label":"mitotic spindle defective early emb"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-061110-61-ZDB-MRPHLNO-120409-1","phenotype":{"types":[{"id":"ZP:0002202","label":"abnormal(ly) edematous whole organism"}]}},{"entity":"ClinVarVariant:3622","phenotype":{"types":[{"id":"HP:0007819","label":"Presenile cataracts"}]}},{"entity":"ClinVarVariant:188235","phenotype":{"types":[{"id":"HP:0100699","label":"Scarring"}]}},{"entity":"ClinVarVariant:40502","phenotype":{"types":[{"id":"HP:0000276","label":"Long face"}]}},{"entity":"ZFIN:ZDB-ALT-040723-8","phenotype":{"types":[{"id":"ZP:0002256","label":"abnormal(ly) distended fourth ventricle"}]}},{"entity":"FlyBase:FBal0143183","phenotype":{"types":[{"id":"FBbt:00004729PHENOTYPE","label":"Drosophila wing phenotype"}]}},{"entity":"ClinVarVariant:11657","phenotype":{"types":[{"id":"HP:0001187","label":"Hyperextensibility of the finger joints"}]}},{"entity":"ClinVarVariant:5462","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"MGI:4431999","phenotype":{"types":[{"id":"HP:0003228","label":"Hypernatremia"}]}},{"entity":"ClinVarVariant:30544","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:35755","phenotype":{"types":[{"id":"HP:0000426","label":"Prominent nasal bridge"}]}},{"entity":"MGI:2445946","phenotype":{"types":[{"id":"MP:0008392","label":"decreased primordial germ cell number"}]}},{"entity":"dbSNP:rs41933638","phenotype":{"types":[{"id":"AQTLTrait:1027","label":"Marbling score"}]}},{"entity":"ClinVarVariant:156148","phenotype":{"types":[{"id":"HP:0001319","label":"Neonatal hypotonia"}]}},{"entity":"ClinVarVariant:5041","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:66431","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"ClinVarVariant:68546","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:2767","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:135705","phenotype":{"types":[{"id":"HP:0100646","label":"Thyroiditis"}]}},{"entity":"FlyBase:FBal0203849","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:100931","phenotype":{"types":[{"id":"HP:0007359","label":"Focal seizures"}]}},{"entity":"MGI:3688879","phenotype":{"types":[{"id":"MP:0010392","label":"prolonged QRS complex duration"}]}},{"entity":"ClinVarVariant:35571","phenotype":{"types":[{"id":"HP:0003073","label":"Hypoalbuminemia"}]}},{"entity":"ClinVarVariant:24365","phenotype":{"types":[{"id":"HP:0000093","label":"Proteinuria"}]}},{"entity":"ClinVarVariant:24419","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:6114","phenotype":{"types":[{"id":"HP:0002510","label":"Spastic tetraplegia"}]}},{"entity":"ClinVarVariant:354","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:11634","phenotype":{"types":[{"id":"HP:0000395","label":"Prominent antihelix"}]}},{"entity":"MGI:3851113","phenotype":{"types":[{"id":"HP:0011472","label":"Abnormality of small intestinal villus morphology"}]}},{"entity":"ClinVarVariant:135899","phenotype":{"types":[{"id":"HP:0000902","label":"Rib fusion"}]}},{"entity":"ClinVarVariant:97681","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"MGI:1857166","phenotype":{"types":[{"id":"HP:0000099","label":"Glomerulonephritis"}]}},{"entity":"MGI:5465004","phenotype":{"types":[{"id":"MP:0011100","label":"preweaning lethality, complete penetrance"}]}},{"entity":"WormBase:WBVar00145415","phenotype":{"types":[{"id":"WBPhenotype:0000695","label":"vulva morphology variant"}]}},{"entity":"ClinVarVariant:189571","phenotype":{"types":[{"id":"HP:0200055","label":"Small hand"}]}},{"entity":"ClinVarVariant:40383","phenotype":{"types":[{"id":"HP:0000962","label":"Hyperkeratosis"}]}},{"entity":"ClinVarVariant:36073","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:49317","phenotype":{"types":[{"id":"HP:0009554","label":"Projection of scalp hair onto lateral cheek"}]}},{"entity":"MGI:1857166","phenotype":{"types":[{"id":"HP:0100494","label":"Abnormality of mast cells"}]}},{"entity":"ClinVarVariant:10725","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"ClinVarVariant:53706","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:68086","phenotype":{"types":[{"id":"HP:0000668","label":"Hypodontia"}]}},{"entity":"MGI:2684151","phenotype":{"types":[{"id":"MP:0000336","label":"decreased mast cell number"}]}},{"entity":"ClinVarVariant:13488","phenotype":{"types":[{"id":"HP:0000776","label":"Congenital diaphragmatic hernia"}]}},{"entity":"ClinVarVariant:42076","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:10987","phenotype":{"types":[{"id":"HP:0002181","label":"Cerebral edema"}]}},{"entity":"ClinVarVariant:7175","phenotype":{"types":[{"id":"HP:0001081","label":"Cholelithiasis"}]}},{"entity":"ClinVarVariant:53953","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:41469","phenotype":{"types":[{"id":"HP:0000239","label":"Large fontanelles"}]}},{"entity":"ClinVarVariant:135726","phenotype":{"types":[{"id":"HP:0007649","label":"Congenital hypertrophy of retinal pigment epithelium"}]}},{"entity":"ClinVarVariant:43595","phenotype":{"types":[{"id":"HP:0030078","label":"Lung adenocarcinoma"}]}},{"entity":"ClinVarVariant:16251","phenotype":{"types":[{"id":"HP:0000869","label":"Secondary amenorrhea"}]}},{"entity":"ClinVarVariant:102","phenotype":{"types":[{"id":"HP:0000987","label":"Atypical scarring of skin"}]}},{"entity":"ClinVarVariant:18054","phenotype":{"types":[{"id":"HP:0002961","label":"Dysgammaglobulinemia"}]}},{"entity":"MGI:2671578","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:136910","phenotype":{"types":[{"id":"HP:0005294","label":"Arterial dissection"}]}},{"entity":"ClinVarVariant:156049","phenotype":{"types":[{"id":"HP:0002019","label":"Constipation"}]}},{"entity":"ClinVarVariant:216494","phenotype":{"types":[{"id":"HP:0001706","label":"Endocardial fibroelastosis"}]}},{"entity":"MGI:2183405","phenotype":{"types":[{"id":"MP:0009230","label":"abnormal sperm head morphology"}]}},{"entity":"ClinVarVariant:10877","phenotype":{"types":[{"id":"HP:0002872","label":"Apneic episodes precipitated by illness, fatigue, stress"}]}},{"entity":"MGI:1856054","phenotype":{"types":[{"id":"MP:0008892","label":"abnormal sperm flagellum morphology"}]}},{"entity":"ClinVarVariant:208832","phenotype":{"types":[{"id":"HP:0001199","label":"Triphalangeal thumb"}]}},{"entity":"ClinVarVariant:39036","phenotype":{"types":[{"id":"HP:0003026","label":"Short long bone"}]}},{"entity":"ClinVarVariant:68695","phenotype":{"types":[{"id":"HP:0001510","label":"Growth delay"}]}},{"entity":"ClinVarVariant:96338","phenotype":{"types":[{"id":"HP:0004523","label":"Long eyebrows"}]}},{"entity":"MGI:4458398","phenotype":{"types":[{"id":"HP:0005403","label":"T lymphocytopenia"}]}},{"entity":"ClinVarVariant:160087","phenotype":{"types":[{"id":"HP:0000280","label":"Coarse facial features"}]}},{"entity":"ClinVarVariant:262","phenotype":{"types":[{"id":"HP:0007759","label":"Opacification of the corneal stroma"}]}},{"entity":"dbSNP:rs41640954","phenotype":{"types":[{"id":"AQTLTrait:1169","label":"Interval to first estrus after calving"}]}},{"entity":"ClinVarVariant:211747","phenotype":{"types":[{"id":"HP:0000268","label":"Dolichocephaly"}]}},{"entity":"ClinVarVariant:53323","phenotype":{"types":[{"id":"HP:0100651","label":"Type I diabetes mellitus"}]}},{"entity":"ClinVarVariant:216220","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:30844","phenotype":{"types":[{"id":"HP:0010442","label":"Polydactyly"}]}},{"entity":"ClinVarVariant:190358","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"AQTL:162","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"AQTL:29894","phenotype":{"types":[{"id":"AQTLTrait:1081","label":"Age at puberty"}]}},{"entity":"ClinVarVariant:35703","phenotype":{"types":[{"id":"HP:0000934","label":"Chondrocalcinosis"}]}},{"entity":"ClinVarVariant:140986","phenotype":{"types":[{"id":"HP:0002035","label":"Rectal prolapse"}]}},{"entity":"ClinVarVariant:67916","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:189951","phenotype":{"types":[{"id":"HP:0005484","label":"Postnatal microcephaly"}]}},{"entity":"ClinVarVariant:41936","phenotype":{"types":[{"id":"HP:0002435","label":"Meningocele"}]}},{"entity":"AQTL:46123","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:180621","phenotype":{"types":[{"id":"HP:0002719","label":"Recurrent infections"}]}},{"entity":"ClinVarVariant:216491","phenotype":{"types":[{"id":"HP:0000567","label":"Chorioretinal coloboma"}]}},{"entity":"ClinVarVariant:158375","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"AQTL:5581","phenotype":{"types":[{"id":"AQTLTrait:1181","label":"Muscle pH"}]}},{"entity":"ClinVarVariant:25006","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"ClinVarVariant:60706","phenotype":{"types":[{"id":"HP:0011904","label":"Persistence of hemoglobin F"}]}},{"entity":"ClinVarVariant:17254","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:159655","phenotype":{"types":[{"id":"HP:0000431","label":"Wide nasal bridge"}]}},{"entity":"ClinVarVariant:918","phenotype":{"types":[{"id":"HP:0002748","label":"Rickets"}]}},{"entity":"ClinVarVariant:1519","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:39504","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:11033","phenotype":{"types":[{"id":"HP:0001598","label":"Concave nail"}]}},{"entity":"ClinVarVariant:208834","phenotype":{"types":[{"id":"HP:0008678","label":"Renal hypoplasia/aplasia"}]}},{"entity":"ClinVarVariant:8371","phenotype":{"types":[{"id":"HP:0030325","label":"Cervicomedullary schisis"}]}},{"entity":"ClinVarVariant:21737","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"FlyBase:FBal0204417","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:210031","phenotype":{"types":[{"id":"HP:0000544","label":"External ophthalmoplegia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00016961-WBRNAi00091176","phenotype":{"types":[{"id":"WBPhenotype:0001422","label":"endocytic transport defect"}]}},{"entity":"ClinVarVariant:92727","phenotype":{"types":[{"id":"HP:0002912","label":"Methylmalonic acidemia"}]}},{"entity":"ClinVarVariant:53660","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:42393","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"ClinVarVariant:209009","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"MGI:5548916","phenotype":{"types":[{"id":"MP:0003921","label":"abnormal heart left ventricle morphology"}]}},{"entity":"ClinVarVariant:13366","phenotype":{"types":[{"id":"HP:0001260","label":"Dysarthria"}]}},{"entity":"MGI:5294798","phenotype":{"types":[{"id":"MP:0011087","label":"neonatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:6678","phenotype":{"types":[{"id":"HP:0009025","label":"Increased connective tissue"}]}},{"entity":"MGI:2176538","phenotype":{"types":[{"id":"MP:0011098","label":"embryonic lethality during organogenesis, complete penetrance"}]}},{"entity":"ClinVarVariant:180631","phenotype":{"types":[{"id":"HP:0001433","label":"Hepatosplenomegaly"}]}},{"entity":"ClinVarVariant:4871","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"ClinVarVariant:189559","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-010724-5-ZDB-MRPHLNO-090818-5","phenotype":{"types":[{"id":"ZP:0000043","label":"abnormal(ly) decreased size eye"}]}},{"entity":"ClinVarVariant:186362","phenotype":{"types":[{"id":"HP:0000824","label":"Growth hormone deficiency"}]}},{"entity":"ClinVarVariant:37138","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"ClinVarVariant:10273","phenotype":{"types":[{"id":"HP:0005681","label":"Juvenile rheumatoid arthritis"}]}},{"entity":"ClinVarVariant:1035","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:65024","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:56203","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:8762","phenotype":{"types":[{"id":"HP:0008066","label":"Abnormal blistering of the skin"}]}},{"entity":"ZFIN:ZDB-ALT-070315-12","phenotype":{"types":[{"id":"ZP:0008827","label":"abnormal(ly) process quality branchiomeric skeletal muscle development"}]}},{"entity":"ClinVarVariant:6212","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:162385","phenotype":{"types":[{"id":"HP:0000998","label":"Hypertrichosis"}]}},{"entity":"dbSNP:rs41607431","phenotype":{"types":[{"id":"AQTLTrait:1115","label":"Chest width"}]}},{"entity":"ClinVarVariant:35706","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:54083","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:183262","phenotype":{"types":[{"id":"HP:0100689","label":"Decreased corneal thickness"}]}},{"entity":"ClinVarVariant:156109","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"MGI:3579250","phenotype":{"types":[{"id":"MP:0000229","label":"abnormal megakaryocyte differentiation"}]}},{"entity":"ClinVarVariant:83199","phenotype":{"types":[{"id":"HP:0006716","label":"Hereditary nonpolyposis colorectal carcinoma"}]}},{"entity":"AQTL:40463","phenotype":{"types":[{"id":"AQTLTrait:1136","label":"Bone quality"}]}},{"entity":"WormBase:WBVar00252381","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:53600","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:93198","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"NCBIGene:474168","phenotype":{"types":[{"id":"HP:0000099","label":"Glomerulonephritis"}]}},{"entity":"ClinVarVariant:194859","phenotype":{"types":[{"id":"HP:0000256","label":"Macrocephaly"}]}},{"entity":"ClinVarVariant:30723","phenotype":{"types":[{"id":"HP:0007360","label":"Aplasia/Hypoplasia of the cerebellum"}]}},{"entity":"ClinVarVariant:25245","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:158580","phenotype":{"types":[{"id":"HP:0002002","label":"Deep philtrum"}]}},{"entity":"MGI:5444021","phenotype":{"types":[{"id":"MP:0001360","label":"abnormal social investigation"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-041212-76-ZDB-MRPHLNO-090513-3","phenotype":{"types":[{"id":"GO:0007368PHENOTYPE","label":"determination of left/right symmetry phenotype"}]}},{"entity":"ClinVarVariant:203516","phenotype":{"types":[{"id":"HP:0002841","label":"Recurrent fungal infections"}]}},{"entity":"ClinVarVariant:160035","phenotype":{"types":[{"id":"HP:0000430","label":"Underdeveloped nasal alae"}]}},{"entity":"ClinVarVariant:137952","phenotype":{"types":[{"id":"HP:0001841","label":"Preaxial foot polydactyly"}]}},{"entity":"ClinVarVariant:41170","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:49531","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:10128","phenotype":{"types":[{"id":"HP:0005542","label":"Prolonged whole-blood clotting time"}]}},{"entity":"ClinVarVariant:179061","phenotype":{"types":[{"id":"HP:0000691","label":"Microdontia"}]}},{"entity":"ClinVarVariant:136113","phenotype":{"types":[{"id":"HP:0000980","label":"Pallor"}]}},{"entity":"ClinVarVariant:198428","phenotype":{"types":[{"id":"HP:0004396","label":"Poor appetite"}]}},{"entity":"ClinVarVariant:92639","phenotype":{"types":[{"id":"HP:0100729","label":"Large face"}]}},{"entity":"ClinVarVariant:53923","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:16873","phenotype":{"types":[{"id":"HP:0002716","label":"Lymphadenopathy"}]}},{"entity":"ClinVarVariant:35866","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"ClinVarVariant:54000","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:53479","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:36062","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"MGI:1934269","phenotype":{"types":[{"id":"HP:0005506","label":"Chronic myelogenous leukemia"}]}},{"entity":"ClinVarVariant:31696","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:1720","phenotype":{"types":[{"id":"HP:0001511","label":"Intrauterine growth retardation"}]}},{"entity":"ClinVarVariant:3193","phenotype":{"types":[{"id":"HP:0008829","label":"Delayed femoral head ossification"}]}},{"entity":"MGI:5538688","phenotype":{"types":[{"id":"HP:0008734","label":"Decreased testicular size"}]}},{"entity":"ClinVarVariant:56181","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:66051","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:16327","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"ClinVarVariant:75243","phenotype":{"types":[{"id":"HP:0100034","label":"Motor tics"}]}},{"entity":"MGI:2679499","phenotype":{"types":[{"id":"GO:0009887PHENOTYPE","label":"organ morphogenesis phenotype"}]}},{"entity":"ClinVarVariant:31210","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:13045","phenotype":{"types":[{"id":"HP:0001123","label":"Visual field defect"}]}},{"entity":"ClinVarVariant:179632","phenotype":{"types":[{"id":"HP:0004937","label":"Pulmonary artery aneurysm"}]}},{"entity":"ClinVarVariant:1866","phenotype":{"types":[{"id":"HP:0002315","label":"Headache"}]}},{"entity":"ClinVarVariant:29652","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ZFIN:ZDB-ALT-980203-386","phenotype":{"types":[{"id":"ZP:0000528","label":"abnormal(ly) decreased size cardiac ventricle"}]}},{"entity":"ClinVarVariant:204218","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:211647","phenotype":{"types":[{"id":"HP:0000776","label":"Congenital diaphragmatic hernia"}]}},{"entity":"ClinVarVariant:67368","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001500-WBRNAi00038528","phenotype":{"types":[{"id":"WBPhenotype:0002046","label":"iron homeostasis variant"}]}},{"entity":"ClinVarVariant:49541","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"MGI:3697906","phenotype":{"types":[{"id":"HP:0000234","label":"Abnormality of the head"}]}},{"entity":"ClinVarVariant:198399","phenotype":{"types":[{"id":"HP:0001279","label":"Syncope"}]}},{"entity":"FlyBase:FBal0294194","phenotype":{"types":[{"id":"FBbt:00004133PHENOTYPE","label":"interommatidial bristle phenotype"}]}},{"entity":"ClinVarVariant:95419","phenotype":{"types":[{"id":"HP:0003487","label":"Babinski sign"}]}},{"entity":"ClinVarVariant:1331","phenotype":{"types":[{"id":"HP:0001395","label":"Hepatic fibrosis"}]}},{"entity":"ClinVarVariant:162400","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"ClinVarVariant:120300","phenotype":{"types":[{"id":"HP:0002071","label":"Abnormality of extrapyramidal motor function"}]}},{"entity":"ClinVarVariant:7315","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"ClinVarVariant:65617","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"MGI:4356015","phenotype":{"types":[{"id":"MP:0005222","label":"abnormal somite size"}]}},{"entity":"ClinVarVariant:24990","phenotype":{"types":[{"id":"HP:0200042","label":"Skin ulcer"}]}},{"entity":"ClinVarVariant:53350","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:1010","phenotype":{"types":[{"id":"HP:0000512","label":"Abnormal electroretinogram"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001186-WBRNAi00086860","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:92545","phenotype":{"types":[{"id":"HP:0002326","label":"Transient ischemic attack"}]}},{"entity":"ClinVarVariant:38726","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:191776","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"FlyBase:FBal0031399","phenotype":{"types":[{"id":"FBbt:00004233PHENOTYPE","label":"Drosophila tertiary pigment cell phenotype"}]}},{"entity":"ClinVarVariant:188299","phenotype":{"types":[{"id":"HP:0010610","label":"Palmar pits"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00044585-WBRNAi00024788","phenotype":{"types":[{"id":"WBPhenotype:0000643","label":"locomotion variant"}]}},{"entity":"ClinVarVariant:42130","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:49521","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"MGI:2137552","phenotype":{"types":[{"id":"MP:0003935","label":"abnormal craniofacial development"}]}},{"entity":"ClinVarVariant:38629","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"ClinVarVariant:143768","phenotype":{"types":[{"id":"HP:0000478","label":"Abnormality of the eye"}]}},{"entity":"ClinVarVariant:24826","phenotype":{"types":[{"id":"HP:0001636","label":"Tetralogy of Fallot"}]}},{"entity":"ClinVarVariant:850","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019835-WBRNAi00082433","phenotype":{"types":[{"id":"WBPhenotype:0001037","label":"sterile progeny"}]}},{"entity":"ClinVarVariant:7185","phenotype":{"types":[{"id":"HP:0002611","label":"Cholestatic liver disease"}]}},{"entity":"ClinVarVariant:17284","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:24656","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"FlyBase:FBal0276873","phenotype":{"types":[{"id":"FBbt:00004508PHENOTYPE","label":"eye phenotype"}]}},{"entity":"AQTL:24787","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:11850","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"MGI:5297423","phenotype":{"types":[{"id":"HP:0001719","label":"Double outlet right ventricle"}]}},{"entity":"ClinVarVariant:12041","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:53725","phenotype":{"types":[{"id":"HP:0004936","label":"Venous thrombosis"}]}},{"entity":"ClinVarVariant:42355","phenotype":{"types":[{"id":"HP:0004933","label":"Ascending aortic dissection"}]}},{"entity":"ClinVarVariant:24265","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"ClinVarVariant:2264","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"MGI:1857632","phenotype":{"types":[{"id":"MP:0004342","label":"scapular bone foramen"}]}},{"entity":"MGI:3526866","phenotype":{"types":[{"id":"MP:0000157","label":"abnormal sternum morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00009498-WBRNAi00085795","phenotype":{"types":[{"id":"WBPhenotype:0001952","label":"germline nuclear positioning variant"}]}},{"entity":"ClinVarVariant:4135","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"ClinVarVariant:54063","phenotype":{"types":[{"id":"HP:0000966","label":"Hypohidrosis"}]}},{"entity":"ClinVarVariant:159076","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:192290","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"ClinVarVariant:167144","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:143120","phenotype":{"types":[{"id":"HP:0000622","label":"Blurred vision"}]}},{"entity":"FlyBase:FBal0294983","phenotype":{"types":[{"id":"FBcv:0000385","label":"short lived"}]}},{"entity":"ClinVarVariant:42317","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"ClinVarVariant:53732","phenotype":{"types":[{"id":"HP:0011947","label":"Respiratory tract infection"}]}},{"entity":"ClinVarVariant:11668","phenotype":{"types":[{"id":"HP:0000498","label":"Blepharitis"}]}},{"entity":"ClinVarVariant:30851","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:13153","phenotype":{"types":[{"id":"HP:0001874","label":"Abnormality of neutrophils"}]}},{"entity":"ClinVarVariant:101354","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"MGI:5522949","phenotype":{"types":[{"id":"MP:0002662","label":"abnormal cauda epididymis morphology"}]}},{"entity":"ClinVarVariant:30182","phenotype":{"types":[{"id":"HP:0003312","label":"Abnormal form of the vertebral bodies"}]}},{"entity":"ClinVarVariant:11114","phenotype":{"types":[{"id":"HP:0001891","label":"Iron deficiency anemia"}]}},{"entity":"ClinVarVariant:10735","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"FlyBase:FBal0095354","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:41334","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:5424","phenotype":{"types":[{"id":"HP:0100750","label":"Atelectasis"}]}},{"entity":"ClinVarVariant:12981","phenotype":{"types":[{"id":"HP:0003324","label":"Generalized muscle weakness"}]}},{"entity":"ClinVarVariant:216845","phenotype":{"types":[{"id":"HP:0001663","label":"Ventricular fibrillation"}]}},{"entity":"ClinVarVariant:142378","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:163768","phenotype":{"types":[{"id":"HP:0000766","label":"Abnormality of the sternum"}]}},{"entity":"ClinVarVariant:40069","phenotype":{"types":[{"id":"HP:0000110","label":"Renal dysplasia"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-060503-240-ZDB-MRPHLNO-101202-1","phenotype":{"types":[{"id":"ZP:0003746","label":"abnormal(ly) delayed angiogenesis"}]}},{"entity":"ClinVarVariant:195329","phenotype":{"types":[{"id":"HP:0000368","label":"Low-set, posteriorly rotated ears"}]}},{"entity":"ClinVarVariant:40249","phenotype":{"types":[{"id":"HP:0100704","label":"Cortical visual impairment"}]}},{"entity":"ClinVarVariant:95454","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:41252","phenotype":{"types":[{"id":"HP:0010298","label":"Smooth tongue"}]}},{"entity":"dbSNP:rs41571256","phenotype":{"types":[{"id":"AQTLTrait:1070","label":"Inseminations per conception"}]}},{"entity":"ClinVarVariant:210016","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:42382","phenotype":{"types":[{"id":"HP:0001380","label":"Ligamentous laxity"}]}},{"entity":"MGI:3530566","phenotype":{"types":[{"id":"HP:0000135","label":"Hypogonadism"}]}},{"entity":"ClinVarVariant:40452","phenotype":{"types":[{"id":"HP:0003510","label":"Severe short stature"}]}},{"entity":"ClinVarVariant:17294","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:36530","phenotype":{"types":[{"id":"HP:0003072","label":"Hypercalcemia"}]}},{"entity":"ClinVarVariant:216568","phenotype":{"types":[{"id":"HP:0002665","label":"Lymphoma"}]}},{"entity":"ClinVarVariant:38909","phenotype":{"types":[{"id":"HP:0003521","label":"Disproportionate short-trunk short stature"}]}},{"entity":"_:genid1939651","phenotype":{"types":[{"id":"ZP:0000335","label":"abnormal(ly) disrupted blood circulation"}]}},{"entity":"ClinVarVariant:42333","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"ClinVarVariant:101286","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:100762","phenotype":{"types":[{"id":"HP:0000174","label":"Abnormality of the palate"}]}},{"entity":"ClinVarVariant:10997","phenotype":{"types":[{"id":"HP:0002181","label":"Cerebral edema"}]}},{"entity":"ClinVarVariant:91680","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:211317","phenotype":{"types":[{"id":"HP:0003312","label":"Abnormal form of the vertebral bodies"}]}},{"entity":"ClinVarVariant:25103","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:159952","phenotype":{"types":[{"id":"HP:0100627","label":"Displacement of the external urethral meatus"}]}},{"entity":"_:genid1976450","phenotype":{"types":[{"id":"ZP:0000038","label":"abnormal(ly) edematous pericardium"}]}},{"entity":"ClinVarVariant:10745","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"dbSNP:rs7756992","phenotype":{"types":[{"id":"HP:0002155","label":"Hypertriglyceridemia"}]}},{"entity":"ClinVarVariant:24583","phenotype":{"types":[{"id":"HP:0010784","label":"Uterine neoplasm"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007008-WBRNAi00064202","phenotype":{"types":[{"id":"WBPhenotype:0000730","label":"apoptosis variant"}]}},{"entity":"ClinVarVariant:9589","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:12788","phenotype":{"types":[{"id":"HP:0011976","label":"Elevated urinary catecholamines"}]}},{"entity":"ClinVarVariant:216729","phenotype":{"types":[{"id":"HP:0100634","label":"Neuroendocrine neoplasm"}]}},{"entity":"MGI:2446069","phenotype":{"types":[{"id":"MP:0008395","label":"abnormal osteoblast differentiation"}]}},{"entity":"ClinVarVariant:14356","phenotype":{"types":[{"id":"HP:0007657","label":"Diffuse nuclear cataract"}]}},{"entity":"ClinVarVariant:7834","phenotype":{"types":[{"id":"HP:0004481","label":"Progressive macrocephaly"}]}},{"entity":"ClinVarVariant:210404","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"WormBase:WBVar00145377","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:16275","phenotype":{"types":[{"id":"HP:0002667","label":"Nephroblastoma (Wilms tumor)"}]}},{"entity":"ClinVarVariant:158319","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:42114","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:210436","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"ClinVarVariant:39026","phenotype":{"types":[{"id":"HP:0003026","label":"Short long bone"}]}},{"entity":"MGI:1856392","phenotype":{"types":[{"id":"HP:0007544","label":"Piebaldism"}]}},{"entity":"dbSNP:rs29010222","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:53535","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000817-WBRNAi00086749","phenotype":{"types":[{"id":"WBPhenotype:0001036","label":"sterile F1"}]}},{"entity":"ClinVarVariant:143264","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"ClinVarVariant:53943","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:53493","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:159024","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"ClinVarVariant:215698","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:55951","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:60536","phenotype":{"types":[{"id":"HP:0002172","label":"Postural instability"}]}},{"entity":"ClinVarVariant:48816","phenotype":{"types":[{"id":"HP:0009720","label":"Adenoma sebaceum"}]}},{"entity":"MGI:3774018","phenotype":{"types":[{"id":"MP:0011087","label":"neonatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:49510","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:56213","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:156160","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"MGI:5646298","phenotype":{"types":[{"id":"HP:0002180","label":"Neurodegeneration"}]}},{"entity":"ClinVarVariant:21525","phenotype":{"types":[{"id":"HP:0001256","label":"Intellectual disability, mild"}]}},{"entity":"ClinVarVariant:4311","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"AQTL:5929","phenotype":{"types":[{"id":"AQTLTrait:1053","label":"Average daily gain"}]}},{"entity":"FlyBase:FBal0269430","phenotype":{"types":[{"id":"FBbt:00002743PHENOTYPE","label":"Drosophila T1 beard phenotype"}]}},{"entity":"ClinVarVariant:31675","phenotype":{"types":[{"id":"HP:0000964","label":"Eczema"}]}},{"entity":"ClinVarVariant:49257","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"NCBIGene:100188011","phenotype":{"types":[{"id":"HP:0002789","label":"Tachypnea"}]}},{"entity":"ClinVarVariant:136120","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"ClinVarVariant:2722","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"FlyBase:FBal0124416","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:156720","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"WormBase:WBVar00248887","phenotype":{"types":[{"id":"WBPhenotype:0000698","label":"vulvaless"}]}},{"entity":"ClinVarVariant:40706","phenotype":{"types":[{"id":"HP:0000027","label":"Azoospermia"}]}},{"entity":"ClinVarVariant:13836","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:56096","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"ClinVarVariant:41513","phenotype":{"types":[{"id":"HP:0002895","label":"Papillary thyroid carcinoma"}]}},{"entity":"ClinVarVariant:17374","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:40493","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:49571","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"NCBIGene:46","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"ClinVarVariant:9303","phenotype":{"types":[{"id":"HP:0000340","label":"Sloping forehead"}]}},{"entity":"ClinVarVariant:3853","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:133101","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:53206","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"dbSNP:rs41937398","phenotype":{"types":[{"id":"AQTLTrait:1101","label":"Foot angle"}]}},{"entity":"ClinVarVariant:10275","phenotype":{"types":[{"id":"HP:0001369","label":"Arthritis"}]}},{"entity":"ClinVarVariant:54004","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:15326","phenotype":{"types":[{"id":"HP:0011031","label":"Abnormality of iron homeostasis"}]}},{"entity":"ClinVarVariant:92555","phenotype":{"types":[{"id":"HP:0002326","label":"Transient ischemic attack"}]}},{"entity":"ClinVarVariant:49551","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:94537","phenotype":{"types":[{"id":"HP:0006466","label":"Ankle contracture"}]}},{"entity":"ClinVarVariant:143160","phenotype":{"types":[{"id":"HP:0003474","label":"Sensory impairment"}]}},{"entity":"ClinVarVariant:135685","phenotype":{"types":[{"id":"HP:0008069","label":"Neoplasm of the skin"}]}},{"entity":"ClinVarVariant:2251","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:1525","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:50993","phenotype":{"types":[{"id":"HP:0009882","label":"Short distal phalanx of finger"}]}},{"entity":"MGI:2678815","phenotype":{"types":[{"id":"MP:0001212","label":"skin lesions"}]}},{"entity":"ClinVarVariant:7155","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001924-WBRNAi00068386","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:92747","phenotype":{"types":[{"id":"HP:0002912","label":"Methylmalonic acidemia"}]}},{"entity":"ClinVarVariant:30040","phenotype":{"types":[{"id":"HP:0000311","label":"Round face"}]}},{"entity":"ClinVarVariant:180277","phenotype":{"types":[{"id":"HP:0001084","label":"Corneal arcus"}]}},{"entity":"ClinVarVariant:36438","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:38950","phenotype":{"types":[{"id":"HP:0001876","label":"Pancytopenia"}]}},{"entity":"ClinVarVariant:93752","phenotype":{"types":[{"id":"HP:0000668","label":"Hypodontia"}]}},{"entity":"ClinVarVariant:14184","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"MGI:4840274","phenotype":{"types":[{"id":"MP:0008185","label":"decreased naive B cell number"}]}},{"entity":"MGI:1857225","phenotype":{"types":[{"id":"MP:0008189","label":"increased transitional stage B cell number"}]}},{"entity":"ClinVarVariant:215688","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:30293","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:4354","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"ClinVarVariant:50061","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:94691","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"ClinVarVariant:189113","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:53297","phenotype":{"types":[{"id":"HP:0001648","label":"Cor pulmonale"}]}},{"entity":"MGI:5463664","phenotype":{"types":[{"id":"HP:0002910","label":"Elevated hepatic transaminases"}]}},{"entity":"ClinVarVariant:188272","phenotype":{"types":[{"id":"HP:0000892","label":"Bifid ribs"}]}},{"entity":"ClinVarVariant:65895","phenotype":{"types":[{"id":"HP:0001392","label":"Abnormality of the liver"}]}},{"entity":"ClinVarVariant:53356","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004010-WBRNAi00063019","phenotype":{"types":[{"id":"WBPhenotype:0000709","label":"pharyngeal morphology variant"}]}},{"entity":"ClinVarVariant:167303","phenotype":{"types":[{"id":"HP:0008368","label":"Tarsal synostosis"}]}},{"entity":"ClinVarVariant:132708","phenotype":{"types":[{"id":"HP:0009919","label":"Retinoblastoma"}]}},{"entity":"ClinVarVariant:36314","phenotype":{"types":[{"id":"HP:0002835","label":"Aspiration"}]}},{"entity":"MGI:1858064","phenotype":{"types":[{"id":"GO:0043473PHENOTYPE","label":"pigmentation phenotype"}]}},{"entity":"ClinVarVariant:49462","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:53481","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:9008","phenotype":{"types":[{"id":"HP:0004383","label":"Hypoplastic left heart"}]}},{"entity":"ClinVarVariant:210444","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ZFIN:ZDB-ALT-040726-6","phenotype":{"types":[{"id":"ZP:0002272","label":"abnormal(ly) necrotic brain"}]}},{"entity":"ClinVarVariant:13693","phenotype":{"types":[{"id":"HP:0001082","label":"Cholecystitis"}]}},{"entity":"ClinVarVariant:133328","phenotype":{"types":[{"id":"HP:0012448","label":"Delayed myelination"}]}},{"entity":"FlyBase:FBal0058766","phenotype":{"types":[{"id":"FBcv:0000386","label":"long lived"}]}},{"entity":"ClinVarVariant:65285","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"MGI:4412094","phenotype":{"types":[{"id":"MP:0000260","label":"abnormal angiogenesis"}]}},{"entity":"ClinVarVariant:66461","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"ClinVarVariant:65104","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:2036","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:4330","phenotype":{"types":[{"id":"HP:0003540","label":"Impaired platelet aggregation"}]}},{"entity":"ClinVarVariant:36092","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"AQTL:15021","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:53931","phenotype":{"types":[{"id":"HP:0003453","label":"Antineutrophil antibody positivity"}]}},{"entity":"ClinVarVariant:210006","phenotype":{"types":[{"id":"HP:0002140","label":"Ischemic stroke"}]}},{"entity":"dbSNP:rs110432080","phenotype":{"types":[{"id":"AQTLTrait:1253","label":"Milk stearic acid percentage"}]}},{"entity":"ClinVarVariant:53690","phenotype":{"types":[{"id":"HP:0011947","label":"Respiratory tract infection"}]}},{"entity":"ClinVarVariant:2568","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:136042","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:9723","phenotype":{"types":[{"id":"HP:0002083","label":"Migraine without aura"}]}},{"entity":"FlyBase:FBal0207483","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:133175","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:68701","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:10144","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:101122","phenotype":{"types":[{"id":"HP:0000490","label":"Deeply set eye"}]}},{"entity":"MGI:3054057","phenotype":{"types":[{"id":"HP:0003110","label":"Abnormality of urine homeostasis"}]}},{"entity":"NCBIGene:100188278","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:38317","phenotype":{"types":[{"id":"HP:0000089","label":"Renal hypoplasia"}]}},{"entity":"ClinVarVariant:2139","phenotype":{"types":[{"id":"HP:0002036","label":"Hiatus hernia"}]}},{"entity":"ClinVarVariant:143572","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:215586","phenotype":{"types":[{"id":"HP:0005550","label":"Chronic lymphatic leukemia"}]}},{"entity":"ClinVarVariant:100930","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:53953","phenotype":{"types":[{"id":"HP:0011950","label":"Bronchiolitis"}]}},{"entity":"ClinVarVariant:82650","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"WormBase:WBVar00242504","phenotype":{"types":[{"id":"WBPhenotype:0000012","label":"dauer constitutive"}]}},{"entity":"ClinVarVariant:65311","phenotype":{"types":[{"id":"HP:0003764","label":"Nevus"}]}},{"entity":"ClinVarVariant:158661","phenotype":{"types":[{"id":"HP:0009937","label":"Facial hirsutism"}]}},{"entity":"ClinVarVariant:30293","phenotype":{"types":[{"id":"HP:0000632","label":"Lacrimation abnormality"}]}},{"entity":"dbSNP:rs109839918","phenotype":{"types":[{"id":"AQTLTrait:1096","label":"Teat length"}]}},{"entity":"ClinVarVariant:39868","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:10014","phenotype":{"types":[{"id":"HP:0030344","label":"Decreased circulating luteinizing hormone level"}]}},{"entity":"ClinVarVariant:145","phenotype":{"types":[{"id":"HP:0001308","label":"Tongue fasciculations"}]}},{"entity":"ClinVarVariant:10692","phenotype":{"types":[{"id":"HP:0100639","label":"Erectile abnormalities"}]}},{"entity":"ClinVarVariant:36096","phenotype":{"types":[{"id":"HP:0001002","label":"Decreased subcutaneous fat"}]}},{"entity":"ClinVarVariant:8643","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"FlyBase:FBal0207769","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017546-WBRNAi00099316","phenotype":{"types":[{"id":"WBPhenotype:0000961","label":"pattern of transgene expression variant"}]}},{"entity":"ClinVarVariant:30964","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001972-WBRNAi00068412","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:143515","phenotype":{"types":[{"id":"HP:0000729","label":"Autistic behavior"}]}},{"entity":"ClinVarVariant:54014","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:45003","phenotype":{"types":[{"id":"HP:0011034","label":"Amyloidosis"}]}},{"entity":"MGI:5286584","phenotype":{"types":[{"id":"HP:0002446","label":"Astrocytosis"}]}},{"entity":"ClinVarVariant:43601","phenotype":{"types":[{"id":"HP:0009726","label":"Renal neoplasm"}]}},{"entity":"OMIM:220210","phenotype":{"types":[{"id":"HP:0010935","label":"Abnormality of the upper urinary tract"}]}},{"entity":"ClinVarVariant:210485","phenotype":{"types":[{"id":"HP:0007327","label":"Mixed demyelinating and axonal polyneuropathy"}]}},{"entity":"ClinVarVariant:36754","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"ClinVarVariant:67997","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"dbSNP:rs1819084","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:12604","phenotype":{"types":[{"id":"HP:0001067","label":"Neurofibromas"}]}},{"entity":"ClinVarVariant:156003","phenotype":{"types":[{"id":"HP:0100533","label":"Inflammatory abnormality of the eye"}]}},{"entity":"ClinVarVariant:25300","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:92575","phenotype":{"types":[{"id":"HP:0002326","label":"Transient ischemic attack"}]}},{"entity":"ClinVarVariant:66481","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"ClinVarVariant:50259","phenotype":{"types":[{"id":"HP:0005897","label":"Severe generalized osteoporosis"}]}},{"entity":"ClinVarVariant:53876","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:208009","phenotype":{"types":[{"id":"HP:0001482","label":"Subcutaneous nodule"}]}},{"entity":"FlyBase:FBal0239575","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004815-WBRNAi00086787","phenotype":{"types":[{"id":"WBPhenotype:0000793","label":"posterior body morphology variant"}]}},{"entity":"ClinVarVariant:101152","phenotype":{"types":[{"id":"HP:0010318","label":"Aplasia/Hypoplasia of the abdominal wall musculature"}]}},{"entity":"ClinVarVariant:97040","phenotype":{"types":[{"id":"HP:0001831","label":"Short toe"}]}},{"entity":"ClinVarVariant:6794","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"dbSNP:rs41859871","phenotype":{"types":[{"id":"AQTLTrait:1292","label":"Early embryonic survival"}]}},{"entity":"ClinVarVariant:10755","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"ClinVarVariant:10609","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:159081","phenotype":{"types":[{"id":"HP:0000752","label":"Hyperactivity"}]}},{"entity":"ClinVarVariant:9973","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:102433","phenotype":{"types":[{"id":"HP:0003128","label":"Lactic acidosis"}]}},{"entity":"MGI:2176174","phenotype":{"types":[{"id":"MP:0011028","label":"impaired branching involved in bronchus morphogenesis"}]}},{"entity":"ClinVarVariant:64987","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"dbSNP:rs4793501","phenotype":{"types":[{"id":"HP:0000539","label":"Abnormality of refraction"}]}},{"entity":"ClinVarVariant:18337","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:36520","phenotype":{"types":[{"id":"HP:0003072","label":"Hypercalcemia"}]}},{"entity":"ClinVarVariant:91670","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"AQTL:10280","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:204086","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"_:genid1972511","phenotype":{"types":[{"id":"ZP:0002787","label":"abnormal(ly) decreased size intestinal epithelium"}]}},{"entity":"FlyBase:FBal0047091","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"MGI:4941848","phenotype":{"types":[{"id":"MP:0003956","label":"abnormal body size"}]}},{"entity":"ClinVarVariant:36381","phenotype":{"types":[{"id":"HP:0001597","label":"Abnormality of the nail"}]}},{"entity":"ClinVarVariant:53524","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"ClinVarVariant:177959","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:53340","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:1379","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:9877","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:7188","phenotype":{"types":[{"id":"HP:0006725","label":"Pancreatic adenocarcinoma"}]}},{"entity":"ClinVarVariant:2149","phenotype":{"types":[{"id":"HP:0002036","label":"Hiatus hernia"}]}},{"entity":"dbSNP:rs11986414","phenotype":{"types":[{"id":"HP:0001433","label":"Hepatosplenomegaly"}]}},{"entity":"ClinVarVariant:13335","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:9946","phenotype":{"types":[{"id":"HP:0001923","label":"Reticulocytosis"}]}},{"entity":"ClinVarVariant:10239","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:3042795","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:90871","phenotype":{"types":[{"id":"HP:0100574","label":"Biliary tract neoplasm"}]}},{"entity":"WormBase:WBVar00146684","phenotype":{"types":[{"id":"WBPhenotype:0001846","label":"phagosome maturation defective"}]}},{"entity":"ClinVarVariant:216715","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006994-WBRNAi00088835","phenotype":{"types":[{"id":"WBPhenotype:0001588","label":"microtubule organization biogenesis variant"}]}},{"entity":"ClinVarVariant:91320","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:65118","phenotype":{"types":[{"id":"HP:0009721","label":"Shagreen patch"}]}},{"entity":"ClinVarVariant:208580","phenotype":{"types":[{"id":"HP:0002414","label":"Spina bifida"}]}},{"entity":"ClinVarVariant:9733","phenotype":{"types":[{"id":"HP:0002083","label":"Migraine without aura"}]}},{"entity":"ClinVarVariant:141815","phenotype":{"types":[{"id":"HP:0002017","label":"Nausea and vomiting"}]}},{"entity":"ClinVarVariant:24826","phenotype":{"types":[{"id":"HP:0001643","label":"Patent ductus arteriosus"}]}},{"entity":"ClinVarVariant:41655","phenotype":{"types":[{"id":"HP:0100730","label":"Bronchogenic cyst"}]}},{"entity":"ClinVarVariant:24361","phenotype":{"types":[{"id":"HP:0200020","label":"Corneal erosion"}]}},{"entity":"FlyBase:FBal0314224","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:2261","phenotype":{"types":[{"id":"HP:0002094","label":"Dyspnea"}]}},{"entity":"ClinVarVariant:10335","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:30910","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"ClinVarVariant:53636","phenotype":{"types":[{"id":"HP:0006510","label":"Chronic obstructive pulmonary disease"}]}},{"entity":"ClinVarVariant:44804","phenotype":{"types":[{"id":"HP:0000368","label":"Low-set, posteriorly rotated ears"}]}},{"entity":"ClinVarVariant:36071","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:2199","phenotype":{"types":[{"id":"HP:0000408","label":"Progressive sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:11934","phenotype":{"types":[{"id":"HP:0002315","label":"Headache"}]}},{"entity":"ClinVarVariant:53728","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:21555","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00019126-WBRNAi00091874","phenotype":{"types":[{"id":"WBPhenotype:0001372","label":"protein DNA interaction variant"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001177-WBRNAi00088701","phenotype":{"types":[{"id":"WBPhenotype:0002059","label":"pore forming toxin hypersensitive"}]}},{"entity":"ClinVarVariant:53284","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000866-WBRNAi00007858","phenotype":{"types":[{"id":"WBPhenotype:0001083","label":"multiple cytoplasmic cavities early emb"}]}},{"entity":"FlyBase:FBal0278276","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:95624","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:819","phenotype":{"types":[{"id":"HP:0200040","label":"Epidermoid cyst"}]}},{"entity":"ClinVarVariant:38806","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"AQTL:49870","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:5142","phenotype":{"types":[{"id":"HP:0000144","label":"Decreased fertility"}]}},{"entity":"ClinVarVariant:53188","phenotype":{"types":[{"id":"HP:0004395","label":"Malnutrition"}]}},{"entity":"ClinVarVariant:194962","phenotype":{"types":[{"id":"HP:0001608","label":"Abnormality of the voice"}]}},{"entity":"ClinVarVariant:159224","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:101105","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"AQTL:11222","phenotype":{"types":[{"id":"AQTLTrait:1027","label":"Marbling score"}]}},{"entity":"ClinVarVariant:64789","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"WormBase:WBVar00250996","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:49591","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"FlyBase:FBal0209601","phenotype":{"types":[{"id":"FBcv:0000385","label":"short lived"}]}},{"entity":"MGI:2678247","phenotype":{"types":[{"id":"MP:0004768","label":"abnormal axonal transport"}]}},{"entity":"ClinVarVariant:30231","phenotype":{"types":[{"id":"HP:0000527","label":"Long eyelashes"}]}},{"entity":"ClinVarVariant:136202","phenotype":{"types":[{"id":"HP:0000750","label":"Delayed speech and language development"}]}},{"entity":"MGI:5620941","phenotype":{"types":[{"id":"MP:0003098","label":"decreased tendon stiffness"}]}},{"entity":"ClinVarVariant:9818","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:38486","phenotype":{"types":[{"id":"HP:0002167","label":"Neurological speech impairment"}]}},{"entity":"ClinVarVariant:210414","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:10727","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"ClinVarVariant:49581","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:16209","phenotype":{"types":[{"id":"HP:0010819","label":"Atonic seizures"}]}},{"entity":"ClinVarVariant:7199","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:36791","phenotype":{"types":[{"id":"HP:0006335","label":"Persistence of primary teeth"}]}},{"entity":"MGI:2429699","phenotype":{"types":[{"id":"HP:0012373","label":"Abnormal eye physiology"}]}},{"entity":"AQTL:16489","phenotype":{"types":[{"id":"AQTLTrait:1173","label":"Rear leg set"}]}},{"entity":"ClinVarVariant:41523","phenotype":{"types":[{"id":"HP:0002895","label":"Papillary thyroid carcinoma"}]}},{"entity":"ClinVarVariant:159218","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"ClinVarVariant:158734","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"ClinVarVariant:156221","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"ClinVarVariant:53913","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:141514","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"MGI:4364926","phenotype":{"types":[{"id":"HP:0011877","label":"Increased mean platelet volume"}]}},{"entity":"MGI:1856226","phenotype":{"types":[{"id":"MP:0001265","label":"decreased body size"}]}},{"entity":"ClinVarVariant:159380","phenotype":{"types":[{"id":"HP:0009890","label":"High anterior hairline"}]}},{"entity":"ClinVarVariant:160081","phenotype":{"types":[{"id":"HP:0001298","label":"Encephalopathy"}]}},{"entity":"FlyBase:FBal0210535","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:127501","phenotype":{"types":[{"id":"HP:0000268","label":"Dolichocephaly"}]}},{"entity":"FlyBase:FBal0242677","phenotype":{"types":[{"id":"FBbt:00002027PHENOTYPE","label":"Drosophila dorsal multidendritic neuron ddaC phenotype"}]}},{"entity":"ClinVarVariant:5539","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"ClinVarVariant:88731","phenotype":{"types":[{"id":"HP:0002307","label":"Drooling"}]}},{"entity":"FlyBase:FBal0230781","phenotype":{"types":[{"id":"FBcv:0002027","label":"lethal - all die before end of pupal stage"}]}},{"entity":"ClinVarVariant:197858","phenotype":{"types":[{"id":"HP:0003300","label":"Ovoid vertebral bodies"}]}},{"entity":"FlyBase:FBal0137561","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:120310","phenotype":{"types":[{"id":"HP:0002071","label":"Abnormality of extrapyramidal motor function"}]}},{"entity":"ClinVarVariant:210018","phenotype":{"types":[{"id":"HP:0009113","label":"Diaphragmatic weakness"}]}},{"entity":"ClinVarVariant:25297","phenotype":{"types":[{"id":"HP:0008209","label":"Premature ovarian failure"}]}},{"entity":"MGI:5527244","phenotype":{"types":[{"id":"HP:0100522","label":"Thymoma"}]}},{"entity":"ClinVarVariant:53175","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"ClinVarVariant:2365","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:4142","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:6915","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:53881","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:94530","phenotype":{"types":[{"id":"HP:0100578","label":"Lipoatrophy"}]}},{"entity":"ClinVarVariant:215763","phenotype":{"types":[{"id":"HP:0100242","label":"Sarcoma"}]}},{"entity":"ClinVarVariant:222","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:10741","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:1113","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:67871","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"MGI:1931047","phenotype":{"types":[{"id":"MP:0010572","label":"persistent right dorsal aorta"}]}},{"entity":"ClinVarVariant:48708","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:30249","phenotype":{"types":[{"id":"HP:0000046","label":"Scrotal hypoplasia"}]}},{"entity":"ClinVarVariant:128250","phenotype":{"types":[{"id":"HP:0002490","label":"Increased CSF lactate"}]}},{"entity":"ClinVarVariant:41075","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"WormBase:WBVar00142906","phenotype":{"types":[{"id":"WBPhenotype:0001516","label":"helical cuticle"}]}},{"entity":"MGI:3837468","phenotype":{"types":[{"id":"HP:0004324","label":"Increased body weight"}]}},{"entity":"WormBase:WBVar00143933","phenotype":{"types":[{"id":"WBPhenotype:0000905","label":"neuron morphology variant"}]}},{"entity":"ClinVarVariant:10078","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"MGI:4442818","phenotype":{"types":[{"id":"MP:0000358","label":"abnormal cell morphology"}]}},{"entity":"MGI:2388594","phenotype":{"types":[{"id":"MP:0006288","label":"small otic capsule"}]}},{"entity":"ClinVarVariant:13172","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"ClinVarVariant:2814","phenotype":{"types":[{"id":"HP:0002435","label":"Meningocele"}]}},{"entity":"ClinVarVariant:49939","phenotype":{"types":[{"id":"HP:0009719","label":"Hypomelanotic macule"}]}},{"entity":"ClinVarVariant:101372","phenotype":{"types":[{"id":"HP:0006323","label":"Premature loss of primary teeth"}]}},{"entity":"ZFIN:ZDB-ALT-121112-2","phenotype":{"types":[{"id":"ZP:0017910","label":"abnormal(ly) disrupted amino-acid betaine transport"}]}},{"entity":"ClinVarVariant:215774","phenotype":{"types":[{"id":"HP:0010743","label":"Short metatarsal"}]}},{"entity":"ClinVarVariant:13713","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:24452","phenotype":{"types":[{"id":"HP:0008619","label":"Bilateral sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:5424","phenotype":{"types":[{"id":"HP:0005222","label":"Bowel diverticulosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001398-WBRNAi00027267","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"MGI:3698412","phenotype":{"types":[{"id":"MP:0008713","label":"abnormal cytokine level"}]}},{"entity":"ClinVarVariant:10706","phenotype":{"types":[{"id":"HP:0002023","label":"Anal atresia"}]}},{"entity":"ClinVarVariant:24666","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"ClinVarVariant:181711","phenotype":{"types":[{"id":"HP:0009765","label":"Low hanging columella"}]}},{"entity":"AQTL:48427","phenotype":{"types":[{"id":"AQTLTrait:1067","label":"Length of productive life"}]}},{"entity":"ClinVarVariant:101259","phenotype":{"types":[{"id":"HP:0000015","label":"Bladder diverticulum"}]}},{"entity":"ClinVarVariant:94681","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"FlyBase:FBal0137126","phenotype":{"types":[{"id":"FBbt:00005200PHENOTYPE","label":"denticle phenotype"}]}},{"entity":"ClinVarVariant:25340","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"ClinVarVariant:6066","phenotype":{"types":[{"id":"HP:0009777","label":"Absent thumb"}]}},{"entity":"ClinVarVariant:54024","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1303","phenotype":{"types":[{"id":"ZP:0000719","label":"abnormal(ly) non-contractile heart"}]}},{"entity":"ClinVarVariant:185817","phenotype":{"types":[{"id":"HP:0002076","label":"Migraine"}]}},{"entity":"ZFIN:ZDB-ALT-980203-1164","phenotype":{"types":[{"id":"ZP:0005400","label":"abnormal(ly) hypoplastic horizontal myoseptum"}]}},{"entity":"ClinVarVariant:30939","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"ClinVarVariant:159249","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:53933","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:67868","phenotype":{"types":[{"id":"HP:0004756","label":"Ventricular tachycardia"}]}},{"entity":"MGI:3525250","phenotype":{"types":[{"id":"MP:0004754","label":"abnormal kidney collecting duct morphology"}]}},{"entity":"ClinVarVariant:42086","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"MGI:3050763","phenotype":{"types":[{"id":"HP:0002180","label":"Neurodegeneration"}]}},{"entity":"ClinVarVariant:7185","phenotype":{"types":[{"id":"HP:0001081","label":"Cholelithiasis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007784-WBRNAi00080092","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:24438","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:194417","phenotype":{"types":[{"id":"HP:0000846","label":"Adrenal insufficiency"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022027-WBRNAi00004763","phenotype":{"types":[{"id":"WBPhenotype:0000644","label":"paralyzed"}]}},{"entity":"ClinVarVariant:159660","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:17484","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"MGI:2183933","phenotype":{"types":[{"id":"MP:0004852","label":"decreased testis weight"}]}},{"entity":"ClinVarVariant:24478","phenotype":{"types":[{"id":"HP:0000517","label":"Abnormality of the lens"}]}},{"entity":"MGI:5440173","phenotype":{"types":[{"id":"HP:0000902","label":"Rib fusion"}]}},{"entity":"ClinVarVariant:186923","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"FlyBase:FBal0242627","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"dbSNP:rs10172646","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:2178057","phenotype":{"types":[{"id":"MP:0001360","label":"abnormal social investigation"}]}},{"entity":"ClinVarVariant:9589","phenotype":{"types":[{"id":"HP:0002352","label":"Leukoencephalopathy"}]}},{"entity":"ClinVarVariant:97524","phenotype":{"types":[{"id":"HP:0000999","label":"Pyoderma"}]}},{"entity":"ClinVarVariant:7411","phenotype":{"types":[{"id":"HP:0001100","label":"Heterochromia iridis"}]}},{"entity":"ClinVarVariant:2218","phenotype":{"types":[{"id":"HP:0100544","label":"Neoplasm of the heart"}]}},{"entity":"FlyBase:FBal0042579","phenotype":{"types":[{"id":"FBcv:0002033","label":"lethal - all die during embryonic stage"}]}},{"entity":"ClinVarVariant:68556","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:5051","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"FlyBase:FBal0284394","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"WormBase:WBVar00089606","phenotype":{"types":[{"id":"WBPhenotype:0000565","label":"coiler"}]}},{"entity":"MGI:2386742","phenotype":{"types":[{"id":"MP:0002834","label":"decreased heart weight"}]}},{"entity":"ClinVarVariant:181956","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"dbSNP:rs1819084","phenotype":{"types":[{"id":"HP:0004798","label":"Recurrent infection of the gastrointestinal tract"}]}},{"entity":"ClinVarVariant:40052","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"ClinVarVariant:120250","phenotype":{"types":[{"id":"HP:0002144","label":"Tethered cord"}]}},{"entity":"ClinVarVariant:53360","phenotype":{"types":[{"id":"HP:0000027","label":"Azoospermia"}]}},{"entity":"MGI:3763247","phenotype":{"types":[{"id":"MP:0002376","label":"abnormal dendritic cell physiology"}]}},{"entity":"dbSNP:rs109025111","phenotype":{"types":[{"id":"AQTLTrait:1153","label":"Stillbirth"}]}},{"entity":"ClinVarVariant:67013","phenotype":{"types":[{"id":"HP:0010536","label":"Central sleep apnea"}]}},{"entity":"ClinVarVariant:4765","phenotype":{"types":[{"id":"HP:0000232","label":"Everted lower lip vermilion"}]}},{"entity":"ClinVarVariant:18242","phenotype":{"types":[{"id":"HP:0009919","label":"Retinoblastoma"}]}},{"entity":"ClinVarVariant:215698","phenotype":{"types":[{"id":"HP:0003468","label":"Abnormality of the vertebrae"}]}},{"entity":"ClinVarVariant:24370","phenotype":{"types":[{"id":"HP:0011508","label":"Macular hole"}]}},{"entity":"ClinVarVariant:11043","phenotype":{"types":[{"id":"HP:0001598","label":"Concave nail"}]}},{"entity":"ClinVarVariant:56602","phenotype":{"types":[{"id":"HP:0007738","label":"Uncontrolled eye movements"}]}},{"entity":"MGI:3811777","phenotype":{"types":[{"id":"MP:0001473","label":"reduced long term potentiation"}]}},{"entity":"ClinVarVariant:7235","phenotype":{"types":[{"id":"HP:0100582","label":"Nasal polyposis"}]}},{"entity":"ClinVarVariant:204077","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:127701","phenotype":{"types":[{"id":"HP:0008204","label":"Precocious puberty with Sertoli cell tumor"}]}},{"entity":"MGI:3513454","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:56677","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"ClinVarVariant:210434","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:66491","phenotype":{"types":[{"id":"HP:0002459","label":"Dysautonomia"}]}},{"entity":"FlyBase:FBal0208645","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:144065","phenotype":{"types":[{"id":"HP:0011484","label":"Posterior synechiae of the anterior chamber"}]}},{"entity":"ClinVarVariant:3914","phenotype":{"types":[{"id":"HP:0003495","label":"GM2-ganglioside accumulation"}]}},{"entity":"ClinVarVariant:1907","phenotype":{"types":[{"id":"HP:0002416","label":"Subependymal cysts"}]}},{"entity":"FlyBase:FBal0097024","phenotype":{"types":[{"id":"FBbt:00001849PHENOTYPE","label":"hypostomal sclerite phenotype"}]}},{"entity":"MGI:2652160","phenotype":{"types":[{"id":"MP:0002452","label":"abnormal professional antigen presenting cell physiology"}]}},{"entity":"MGI:1926453","phenotype":{"types":[{"id":"MP:0003704","label":"abnormal hair follicle development"}]}},{"entity":"ClinVarVariant:6272","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"FlyBase:FBal0296336","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:65525","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"MGI:1861040","phenotype":{"types":[{"id":"MP:0002389","label":"abnormal Peyer's patch follicle morphology"}]}},{"entity":"ClinVarVariant:3491","phenotype":{"types":[{"id":"HP:0003774","label":"Stage 5 chronic kidney disease"}]}},{"entity":"ClinVarVariant:140916","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"ClinVarVariant:95085","phenotype":{"types":[{"id":"HP:0000954","label":"Single transverse palmar crease"}]}},{"entity":"ClinVarVariant:1470","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:189700","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:35858","phenotype":{"types":[{"id":"HP:0006516","label":"Hypersensitivity pneumonitis"}]}},{"entity":"MGI:2389582","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:135777","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"MGI:2429736","phenotype":{"types":[{"id":"MP:0010776","label":"abnormal placenta metrial gland morphology"}]}},{"entity":"ClinVarVariant:6652","phenotype":{"types":[{"id":"HP:0003741","label":"Congenital muscular dystrophy"}]}},{"entity":"ClinVarVariant:204093","phenotype":{"types":[{"id":"HP:0000112","label":"Nephropathy"}]}},{"entity":"ClinVarVariant:132711","phenotype":{"types":[{"id":"HP:0000706","label":"Unerupted tooth"}]}},{"entity":"_:genid1976000","phenotype":{"types":[{"id":"ZP:0000765","label":"abnormal(ly) increased size optic tectum"}]}},{"entity":"ClinVarVariant:188879","phenotype":{"types":[{"id":"HP:0200032","label":"Kayser-Fleischer ring"}]}},{"entity":"ClinVarVariant:5279","phenotype":{"types":[{"id":"HP:0010978","label":"Abnormality of immune system physiology"}]}},{"entity":"ClinVarVariant:136102","phenotype":{"types":[{"id":"HP:0010829","label":"Impaired temperature sensation"}]}},{"entity":"ClinVarVariant:11456","phenotype":{"types":[{"id":"HP:0000679","label":"Taurodontia"}]}},{"entity":"MGI:5471642","phenotype":{"types":[{"id":"MP:0006042","label":"increased apoptosis"}]}},{"entity":"ClinVarVariant:42357","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"ClinVarVariant:40245","phenotype":{"types":[{"id":"HP:0100775","label":"Dural ectasia"}]}},{"entity":"ClinVarVariant:188801","phenotype":{"types":[{"id":"HP:0001933","label":"Subcutaneous hemorrhage"}]}},{"entity":"ClinVarVariant:180636","phenotype":{"types":[{"id":"HP:0001339","label":"Lissencephaly"}]}},{"entity":"ClinVarVariant:31017","phenotype":{"types":[{"id":"HP:0006439","label":"Radioulnar dislocation"}]}},{"entity":"ClinVarVariant:38932","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:13997","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:155793","phenotype":{"types":[{"id":"HP:0001646","label":"Abnormality of the aortic valve"}]}},{"entity":"ClinVarVariant:10108","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"ClinVarVariant:17346","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"MGI:5297423","phenotype":{"types":[{"id":"HP:0011641","label":"Coronary artery fistula"}]}},{"entity":"dbSNP:rs80934742","phenotype":{"types":[{"id":"AQTLTrait:1181","label":"Muscle pH"}]}},{"entity":"ClinVarVariant:49414","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"NCBIGene:105463128","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"ClinVarVariant:36381","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:1529","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:1087","phenotype":{"types":[{"id":"HP:0001371","label":"Flexion contracture"}]}},{"entity":"ClinVarVariant:184154","phenotype":{"types":[{"id":"HP:0001920","label":"Renal artery stenosis"}]}},{"entity":"FlyBase:FBal0127293","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:67926","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:3961","phenotype":{"types":[{"id":"HP:0000652","label":"Lower eyelid coloboma"}]}},{"entity":"ClinVarVariant:40983","phenotype":{"types":[{"id":"HP:0003025","label":"Metaphyseal irregularity"}]}},{"entity":"ClinVarVariant:3282","phenotype":{"types":[{"id":"HP:0010302","label":"Spinal cord tumor"}]}},{"entity":"ClinVarVariant:1825","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:1115","phenotype":{"types":[{"id":"HP:0000608","label":"Macular degeneration"}]}},{"entity":"ClinVarVariant:25059","phenotype":{"types":[{"id":"HP:0100275","label":"Diffuse cerebellar atrophy"}]}},{"entity":"ClinVarVariant:197758","phenotype":{"types":[{"id":"HP:0001685","label":"Myocardial fibrosis"}]}},{"entity":"ClinVarVariant:210424","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000390-WBRNAi00034721","phenotype":{"types":[{"id":"WBPhenotype:0000700","label":"multivulva"}]}},{"entity":"ClinVarVariant:8953","phenotype":{"types":[{"id":"HP:0000126","label":"Hydronephrosis"}]}},{"entity":"FlyBase:FBal0200755","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:100775","phenotype":{"types":[{"id":"HP:0001371","label":"Flexion contracture"}]}},{"entity":"ClinVarVariant:8746","phenotype":{"types":[{"id":"HP:0009908","label":"Anterior creases of earlobe"}]}},{"entity":"ClinVarVariant:53456","phenotype":{"types":[{"id":"HP:0006538","label":"Recurrent bronchopulmonary infections"}]}},{"entity":"ClinVarVariant:216771","phenotype":{"types":[{"id":"HP:0002385","label":"Paraparesis"}]}},{"entity":"ZFIN:ZDB-ALT-150115-1","phenotype":{"types":[{"id":"ZP:0013924","label":"abnormal(ly) has fewer parts of type spinal cord motor neuron towards motor neuron synapse"}]}},{"entity":"ClinVarVariant:12483","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"ClinVarVariant:41057","phenotype":{"types":[{"id":"HP:0010297","label":"Bifid tongue"}]}},{"entity":"ClinVarVariant:24459","phenotype":{"types":[{"id":"HP:0100273","label":"Neoplasm of the colon"}]}},{"entity":"ClinVarVariant:41112","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:17292","phenotype":{"types":[{"id":"HP:0001518","label":"Small for gestational age"}]}},{"entity":"ClinVarVariant:11826","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"MGI:3526854","phenotype":{"types":[{"id":"MP:0010587","label":"conotruncal ridge hypoplasia"}]}},{"entity":"ClinVarVariant:4024","phenotype":{"types":[{"id":"HP:0000158","label":"Macroglossia"}]}},{"entity":"ClinVarVariant:126402","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:53518","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"NCBIGene:46","phenotype":{"types":[{"id":"HP:0000463","label":"Anteverted nares"}]}},{"entity":"ClinVarVariant:25235","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"FlyBase:FBal0208051","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:31215","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"MGI:3702579","phenotype":{"types":[{"id":"HP:0005403","label":"T lymphocytopenia"}]}},{"entity":"FlyBase:FBal0042742","phenotype":{"types":[{"id":"FBcv:0002041","label":"some die during embryonic stage"}]}},{"entity":"NCBIGene:2759","phenotype":{"types":[{"id":"HP:0001943","label":"Hypoglycemia"}]}},{"entity":"dbSNP:rs43015698","phenotype":{"types":[{"id":"AQTLTrait:1327","label":"Milk odd-chain fatty acid percentage"}]}},{"entity":"ClinVarVariant:13664","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:101165","phenotype":{"types":[{"id":"HP:0100645","label":"Cystocele"}]}},{"entity":"ClinVarVariant:120291","phenotype":{"types":[{"id":"HP:0001992","label":"Organic aciduria"}]}},{"entity":"ClinVarVariant:10888","phenotype":{"types":[{"id":"HP:0000496","label":"Abnormality of eye movement"}]}},{"entity":"ClinVarVariant:12783","phenotype":{"types":[{"id":"HP:0002668","label":"Paraganglioma"}]}},{"entity":"ClinVarVariant:189202","phenotype":{"types":[{"id":"HP:0001662","label":"Bradycardia"}]}},{"entity":"ClinVarVariant:1114","phenotype":{"types":[{"id":"HP:0001258","label":"Spastic paraplegia"}]}},{"entity":"ClinVarVariant:53933","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:49975","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"MGI:3692444","phenotype":{"types":[{"id":"MP:0011089","label":"perinatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:53448","phenotype":{"types":[{"id":"HP:0100646","label":"Thyroiditis"}]}},{"entity":"ClinVarVariant:101175","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:188802","phenotype":{"types":[{"id":"HP:0100022","label":"Abnormality of movement"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-070206-1-ZDB-MRPHLNO-120719-3","phenotype":{"types":[{"id":"ZP:0003863","label":"abnormal(ly) malformed caudal vein plexus"}]}},{"entity":"FlyBase:FBal0267174","phenotype":{"types":[{"id":"FBcv:0000425","label":"increased cell death"}]}},{"entity":"ClinVarVariant:159086","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:41388","phenotype":{"types":[{"id":"HP:0008069","label":"Neoplasm of the skin"}]}},{"entity":"ClinVarVariant:132731","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:132873","phenotype":{"types":[{"id":"HP:0005059","label":"Arthralgia/arthritis"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-040704-56-ZDB-MRPHLNO-150717-3","phenotype":{"types":[{"id":"GO:0001654PHENOTYPE","label":"eye development phenotype"}]}},{"entity":"dbSNP:rs135873847","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"MGI:1856333","phenotype":{"types":[{"id":"MP:0008917","label":"abnormal oligodendrocyte physiology"}]}},{"entity":"ClinVarVariant:21109","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:95186","phenotype":{"types":[{"id":"HP:0002793","label":"Abnormal pattern of respiration"}]}},{"entity":"ClinVarVariant:2931","phenotype":{"types":[{"id":"HP:0010628","label":"Facial palsy"}]}},{"entity":"FlyBase:FBal0206992","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:53489","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:54034","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"MGI:1926453","phenotype":{"types":[{"id":"MP:0000424","label":"retarded hair growth"}]}},{"entity":"MGI:3577203","phenotype":{"types":[{"id":"MP:0006082","label":"CNS inflammation"}]}},{"entity":"ClinVarVariant:162523","phenotype":{"types":[{"id":"HP:0010055","label":"Broad hallux"}]}},{"entity":"dbSNP:rs1864400","phenotype":{"types":[{"id":"HP:0004401","label":"Meconium ileus"}]}},{"entity":"ClinVarVariant:50259","phenotype":{"types":[{"id":"HP:0002756","label":"Pathologic fracture"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000063-WBRNAi00026183","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"_:genid1974640","phenotype":{"types":[{"id":"ZP:0001504","label":"abnormal(ly) present in fewer numbers in organism myotome skeletal muscle cell"}]}},{"entity":"ClinVarVariant:91660","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:215589","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:102846","phenotype":{"types":[{"id":"HP:0003231","label":"Hypertyrosinemia"}]}},{"entity":"ClinVarVariant:30013","phenotype":{"types":[{"id":"HP:0000294","label":"Low anterior hairline"}]}},{"entity":"ClinVarVariant:10664","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"MGI:3693248","phenotype":{"types":[{"id":"GO:0008016PHENOTYPE","label":"regulation of heart contraction phenotype"}]}},{"entity":"FlyBase:FBal0246629","phenotype":{"types":[{"id":"GO:0030054PHENOTYPE","label":"cell junction phenotype"}]}},{"entity":"MGI:2179534","phenotype":{"types":[{"id":"HP:0001629","label":"Ventricular septal defect"}]}},{"entity":"MGI:3689957","phenotype":{"types":[{"id":"MP:0010205","label":"abnormal oligodendrocyte apoptosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007352-WBRNAi00079985","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011747-WBRNAi00073828","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:53610","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:10551","phenotype":{"types":[{"id":"HP:0000597","label":"Ophthalmoparesis"}]}},{"entity":"ClinVarVariant:53330","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:10318","phenotype":{"types":[{"id":"HP:0100614","label":"Myositis"}]}},{"entity":"ClinVarVariant:10063","phenotype":{"types":[{"id":"HP:0007325","label":"Generalized dystonia"}]}},{"entity":"MGI:2183949","phenotype":{"types":[{"id":"HP:0011902","label":"Abnormal hemoglobin"}]}},{"entity":"ClinVarVariant:10736","phenotype":{"types":[{"id":"HP:0000503","label":"Tortuosity of conjunctival vessels"}]}},{"entity":"ClinVarVariant:24650","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:177834","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"MGI:3701835","phenotype":{"types":[{"id":"HP:0003687","label":"Centrally nucleated skeletal muscle fibers"}]}},{"entity":"ClinVarVariant:11520","phenotype":{"types":[{"id":"HP:0002007","label":"Frontal bossing"}]}},{"entity":"ClinVarVariant:17491","phenotype":{"types":[{"id":"HP:0000360","label":"Tinnitus"}]}},{"entity":"ClinVarVariant:7445","phenotype":{"types":[{"id":"HP:0100896","label":"Rectal polyposis"}]}},{"entity":"ClinVarVariant:161357","phenotype":{"types":[{"id":"HP:0001166","label":"Arachnodactyly"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004453-WBRNAi00085642","phenotype":{"types":[{"id":"WBPhenotype:0000291","label":"no oocytes"}]}},{"entity":"MGI:2181662","phenotype":{"types":[{"id":"MP:0008515","label":"thin retinal outer nuclear layer"}]}},{"entity":"_:genid1975883","phenotype":{"types":[{"id":"ZP:0000319","label":"abnormal(ly) hydrocephalic brain"}]}},{"entity":"ClinVarVariant:7519","phenotype":{"types":[{"id":"HP:0001265","label":"Hyporeflexia"}]}},{"entity":"MGI:3655845","phenotype":{"types":[{"id":"HP:0007033","label":"Cerebellar dysplasia"}]}},{"entity":"ClinVarVariant:12038","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"_:genid1938554","phenotype":{"types":[{"id":"ZP:0000473","label":"abnormal(ly) decreased length whole organism"}]}},{"entity":"ClinVarVariant:162387","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"MGI:3830289","phenotype":{"types":[{"id":"HP:0001669","label":"Transposition of the great arteries"}]}},{"entity":"dbSNP:rs1953600","phenotype":{"types":[{"id":"HP:0006516","label":"Hypersensitivity pneumonitis"}]}},{"entity":"FlyBase:FBal0199757","phenotype":{"types":[{"id":"FBbt:00004580PHENOTYPE","label":"Drosophila mesothoracic tergum phenotype"}]}},{"entity":"ClinVarVariant:204228","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:1901","phenotype":{"types":[{"id":"HP:0007360","label":"Aplasia/Hypoplasia of the cerebellum"}]}},{"entity":"ClinVarVariant:101364","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"MGI:5641735","phenotype":{"types":[{"id":"MP:0000877","label":"abnormal Purkinje cell morphology"}]}},{"entity":"ClinVarVariant:35895","phenotype":{"types":[{"id":"HP:0006706","label":"Cystic liver disease"}]}},{"entity":"ClinVarVariant:8733","phenotype":{"types":[{"id":"HP:0003128","label":"Lactic acidosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003073-WBRNAi00034975","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:11667","phenotype":{"types":[{"id":"HP:0001187","label":"Hyperextensibility of the finger joints"}]}},{"entity":"FlyBase:FBal0197891","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:143534","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"ClinVarVariant:41696","phenotype":{"types":[{"id":"HP:0009734","label":"Optic glioma"}]}},{"entity":"ClinVarVariant:64974","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:7440","phenotype":{"types":[{"id":"HP:0000069","label":"Abnormality of the ureter"}]}},{"entity":"dbSNP:rs43703486","phenotype":{"types":[{"id":"AQTLTrait:1096","label":"Teat length"}]}},{"entity":"ClinVarVariant:13351","phenotype":{"types":[{"id":"HP:0000391","label":"Thickened helices"}]}},{"entity":"ClinVarVariant:65898","phenotype":{"types":[{"id":"HP:0000939","label":"Osteoporosis"}]}},{"entity":"ClinVarVariant:10068","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"WormBase:WBVar00088666","phenotype":{"types":[{"id":"WBPhenotype:0000012","label":"dauer constitutive"}]}},{"entity":"ClinVarVariant:56031","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:5559","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"MGI:2176775","phenotype":{"types":[{"id":"MP:0002169","label":"no abnormal phenotype detected"}]}},{"entity":"ClinVarVariant:782","phenotype":{"types":[{"id":"HP:0003201","label":"Rhabdomyolysis"}]}},{"entity":"WormBase:WBVar00088241","phenotype":{"types":[{"id":"WBPhenotype:0001351","label":"protein phosphorylation reduced"}]}},{"entity":"ClinVarVariant:42327","phenotype":{"types":[{"id":"HP:0001704","label":"Tricuspid valve prolapse"}]}},{"entity":"ClinVarVariant:217027","phenotype":{"types":[{"id":"HP:0000682","label":"Abnormality of dental enamel"}]}},{"entity":"ClinVarVariant:38314","phenotype":{"types":[{"id":"HP:0000046","label":"Scrotal hypoplasia"}]}},{"entity":"ClinVarVariant:7926","phenotype":{"types":[{"id":"HP:0007856","label":"Punctate opacification of the cornea"}]}},{"entity":"ClinVarVariant:53670","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:101202","phenotype":{"types":[{"id":"HP:0005267","label":"Premature delivery because of cervical insufficiency or membrane fragility"}]}},{"entity":"MGI:2450853","phenotype":{"types":[{"id":"HP:0000798","label":"Oligospermia"}]}},{"entity":"ClinVarVariant:136171","phenotype":{"types":[{"id":"HP:0002044","label":"Zollinger-Ellison syndrome"}]}},{"entity":"ClinVarVariant:210444","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:38425","phenotype":{"types":[{"id":"HP:0003264","label":"Deficiency of N-acetylglucosamine-1-phosphotransferase"}]}},{"entity":"ClinVarVariant:96","phenotype":{"types":[{"id":"HP:0000153","label":"Abnormality of the mouth"}]}},{"entity":"ClinVarVariant:24380","phenotype":{"types":[{"id":"HP:0100242","label":"Sarcoma"}]}},{"entity":"ClinVarVariant:7789","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"MGI:2667333","phenotype":{"types":[{"id":"HP:0002733","label":"Abnormality of the lymph nodes"}]}},{"entity":"ClinVarVariant:5590","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:209077","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:2116","phenotype":{"types":[{"id":"HP:0002510","label":"Spastic tetraplegia"}]}},{"entity":"ClinVarVariant:208182","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:54093","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:982","phenotype":{"types":[{"id":"HP:0005105","label":"Abnormal nasal morphology"}]}},{"entity":"ClinVarVariant:39785","phenotype":{"types":[{"id":"HP:0000592","label":"Blue sclerae"}]}},{"entity":"ClinVarVariant:41202","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:11096","phenotype":{"types":[{"id":"HP:0010307","label":"Stridor"}]}},{"entity":"ClinVarVariant:192241","phenotype":{"types":[{"id":"HP:0000734","label":"Disinhibition"}]}},{"entity":"ClinVarVariant:50030","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"dbSNP:rs1953600","phenotype":{"types":[{"id":"HP:0011134","label":"Low-grade fever"}]}},{"entity":"MGI:2678819","phenotype":{"types":[{"id":"MP:0008083","label":"decreased single-positive T cell number"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00044800-WBRNAi00085802","phenotype":{"types":[{"id":"WBPhenotype:0000186","label":"oogenesis variant"}]}},{"entity":"MGI:5293082","phenotype":{"types":[{"id":"HP:0002910","label":"Elevated hepatic transaminases"}]}},{"entity":"ClinVarVariant:209047","phenotype":{"types":[{"id":"HP:0002331","label":"Headache (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:13349","phenotype":{"types":[{"id":"HP:0000465","label":"Webbed neck"}]}},{"entity":"ClinVarVariant:16262","phenotype":{"types":[{"id":"HP:0003759","label":"Hypoplasia of lymphatic vessels"}]}},{"entity":"ClinVarVariant:4320","phenotype":{"types":[{"id":"HP:0003540","label":"Impaired platelet aggregation"}]}},{"entity":"ClinVarVariant:137948","phenotype":{"types":[{"id":"HP:0000768","label":"Pectus carinatum"}]}},{"entity":"ClinVarVariant:11124","phenotype":{"types":[{"id":"HP:0001891","label":"Iron deficiency anemia"}]}},{"entity":"ClinVarVariant:212207","phenotype":{"types":[{"id":"HP:0002015","label":"Dysphagia"}]}},{"entity":"ClinVarVariant:5194","phenotype":{"types":[{"id":"HP:0002694","label":"Sclerosis of skull base"}]}},{"entity":"ClinVarVariant:65750","phenotype":{"types":[{"id":"HP:0001875","label":"Neutropenia"}]}},{"entity":"ClinVarVariant:3843","phenotype":{"types":[{"id":"HP:0003109","label":"Hyperphosphaturia"}]}},{"entity":"ClinVarVariant:279","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"ClinVarVariant:65513","phenotype":{"types":[{"id":"HP:0000546","label":"Retinal degeneration"}]}},{"entity":"ClinVarVariant:2146","phenotype":{"types":[{"id":"HP:0001377","label":"Limited elbow extension"}]}},{"entity":"FlyBase:FBal0175418","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"FlyBase:FBal0203926","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:208026","phenotype":{"types":[{"id":"HP:0000280","label":"Coarse facial features"}]}},{"entity":"ClinVarVariant:10232","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"ClinVarVariant:200129","phenotype":{"types":[{"id":"HP:0004937","label":"Pulmonary artery aneurysm"}]}},{"entity":"ClinVarVariant:53494","phenotype":{"types":[{"id":"HP:0006528","label":"Chronic lung disease"}]}},{"entity":"ClinVarVariant:5069","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:5145","phenotype":{"types":[{"id":"HP:0008625","label":"Severe sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:40594","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ZFIN:ZDB-ALT-060301-2","phenotype":{"types":[{"id":"ZP:0012481","label":"abnormal(ly) decreased cellular motility branchiomotor neuron"}]}},{"entity":"ClinVarVariant:6292","phenotype":{"types":[{"id":"HP:0002750","label":"Delayed skeletal maturation"}]}},{"entity":"ClinVarVariant:24279","phenotype":{"types":[{"id":"HP:0000613","label":"Photophobia"}]}},{"entity":"ClinVarVariant:10765","phenotype":{"types":[{"id":"HP:0002039","label":"Anorexia"}]}},{"entity":"MGI:3689422","phenotype":{"types":[{"id":"MP:0008302","label":"thin adrenal cortex"}]}},{"entity":"MGI:2387343","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"MGI:3056733","phenotype":{"types":[{"id":"MP:0009820","label":"abnormal liver vasculature morphology"}]}},{"entity":"ClinVarVariant:7215","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:92592","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"MGI:3810526","phenotype":{"types":[{"id":"HP:0005404","label":"Increase in B cell number"}]}},{"entity":"ClinVarVariant:190250","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:215683","phenotype":{"types":[{"id":"HP:0100246","label":"Osteoma"}]}},{"entity":"ClinVarVariant:14924","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:72","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"FlyBase:FBal0262639","phenotype":{"types":[{"id":"FBbt:00000052PHENOTYPE","label":"Drosophila embryo phenotype"}]}},{"entity":"FlyBase:FBal0104352","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"FlyBase:FBal0125070","phenotype":{"types":[{"id":"FBbt:00004511PHENOTYPE","label":"Drosophila antenna phenotype"}]}},{"entity":"MGI:1856555","phenotype":{"types":[{"id":"MP:0004528","label":"fused outer hair cell stereocilia"}]}},{"entity":"ClinVarVariant:132644","phenotype":{"types":[{"id":"HP:0003108","label":"Hyperglycinuria"}]}},{"entity":"ClinVarVariant:67509","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"MGI:5507843","phenotype":{"types":[{"id":"MP:0002084","label":"abnormal developmental patterning"}]}},{"entity":"ClinVarVariant:183434","phenotype":{"types":[{"id":"HP:0000358","label":"Posteriorly rotated ears"}]}},{"entity":"MGI:2183515","phenotype":{"types":[{"id":"MP:0011100","label":"preweaning lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:36320","phenotype":{"types":[{"id":"HP:0011906","label":"Reduced beta/alpha synthesis ratio"}]}},{"entity":"ClinVarVariant:10859","phenotype":{"types":[{"id":"HP:0000733","label":"Stereotypic behavior"}]}},{"entity":"AQTL:54067","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:13351","phenotype":{"types":[{"id":"HP:0010935","label":"Abnormality of the upper urinary tract"}]}},{"entity":"ClinVarVariant:158279","phenotype":{"types":[{"id":"HP:0006191","label":"Deep palmar crease"}]}},{"entity":"ClinVarVariant:41145","phenotype":{"types":[{"id":"HP:0000286","label":"Epicanthus"}]}},{"entity":"ClinVarVariant:185834","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:1856328","phenotype":{"types":[{"id":"MP:0013237","label":"abnormal skeletal muscle regeneration"}]}},{"entity":"ClinVarVariant:217049","phenotype":{"types":[{"id":"HP:0000997","label":"Axillary freckling"}]}},{"entity":"ClinVarVariant:12690","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:13949","phenotype":{"types":[{"id":"HP:0000843","label":"Hyperparathyroidism"}]}},{"entity":"MGI:1856197","phenotype":{"types":[{"id":"MP:0006371","label":"absent hair follicle pheomelanosome pheomelanin"}]}},{"entity":"ClinVarVariant:53229","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"ClinVarVariant:143582","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:210446","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"ClinVarVariant:10146","phenotype":{"types":[{"id":"HP:0005261","label":"Joint hemorrhage"}]}},{"entity":"ClinVarVariant:54044","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"MGI:1856009","phenotype":{"types":[{"id":"HP:0000855","label":"Insulin resistance"}]}},{"entity":"ClinVarVariant:40680","phenotype":{"types":[{"id":"HP:0001595","label":"Abnormality of the hair"}]}},{"entity":"ClinVarVariant:167487","phenotype":{"types":[{"id":"HP:0005576","label":"Tubulointerstitial fibrosis"}]}},{"entity":"ClinVarVariant:17322","phenotype":{"types":[{"id":"HP:0002659","label":"Increased susceptibility to fractures"}]}},{"entity":"ClinVarVariant:8212","phenotype":{"types":[{"id":"HP:0100730","label":"Bronchogenic cyst"}]}},{"entity":"ClinVarVariant:156529","phenotype":{"types":[{"id":"HP:0011950","label":"Bronchiolitis"}]}},{"entity":"ClinVarVariant:210464","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:159157","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"ClinVarVariant:25225","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"MGI:1889570","phenotype":{"types":[{"id":"GO:0006112PHENOTYPE","label":"energy reserve metabolic process phenotype"}]}},{"entity":"ClinVarVariant:53366","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:167138","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:30835","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"NCBIGene:100188340","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:906","phenotype":{"types":[{"id":"HP:0002721","label":"Immunodeficiency"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-991124-7-ZDB-MRPHLNO-060328-3","phenotype":{"types":[{"id":"ZP:0008625","label":"abnormal(ly) physical object quality pectoral fin"}]}},{"entity":"MGI:2182273","phenotype":{"types":[{"id":"HP:0005403","label":"T lymphocytopenia"}]}},{"entity":"ClinVarVariant:2712","phenotype":{"types":[{"id":"HP:0000268","label":"Dolichocephaly"}]}},{"entity":"ClinVarVariant:1655","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:49520","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:159216","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:180362","phenotype":{"types":[{"id":"HP:0000166","label":"Severe periodontitis"}]}},{"entity":"ClinVarVariant:2687","phenotype":{"types":[{"id":"HP:0001297","label":"Stroke"}]}},{"entity":"ClinVarVariant:41224","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ClinVarVariant:190257","phenotype":{"types":[{"id":"HP:0100646","label":"Thyroiditis"}]}},{"entity":"ClinVarVariant:4364","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"ClinVarVariant:143482","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:36962","phenotype":{"types":[{"id":"HP:0002652","label":"Skeletal dysplasia"}]}},{"entity":"ClinVarVariant:65377","phenotype":{"types":[{"id":"HP:0009734","label":"Optic glioma"}]}},{"entity":"FlyBase:FBal0051183","phenotype":{"types":[{"id":"FBcv:0002000","label":"lethal - all die before end of P-stage"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050208-123-ZDB-MRPHLNO-150410-1-ZDB-MRPHLNO-150424-1","phenotype":{"types":[{"id":"ZP:0001849","label":"abnormal(ly) present in greater numbers in organism pronephros multi-ciliated epithelial cell"}]}},{"entity":"ClinVarVariant:103","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:6619","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"AQTL:44271","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:40555","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:12483","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"ClinVarVariant:41882","phenotype":{"types":[{"id":"HP:0001321","label":"Cerebellar hypoplasia"}]}},{"entity":"ClinVarVariant:42347","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"MGI:2384332","phenotype":{"types":[{"id":"MP:0003921","label":"abnormal heart left ventricle morphology"}]}},{"entity":"ClinVarVariant:53206","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:24468","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:16424","phenotype":{"types":[{"id":"HP:0100749","label":"Chest pain"}]}},{"entity":"ClinVarVariant:16875","phenotype":{"types":[{"id":"HP:0003325","label":"Limb-girdle muscle weakness"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-030127-1-ZDB-MRPHLNO-051221-6","phenotype":{"types":[{"id":"ZP:0000132","label":"abnormal(ly) malformed ceratohyal cartilage"}]}},{"entity":"ClinVarVariant:53974","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:53710","phenotype":{"types":[{"id":"HP:0011892","label":"Vitamin K deficiency"}]}},{"entity":"ClinVarVariant:142434","phenotype":{"types":[{"id":"HP:0002073","label":"Progressive cerebellar ataxia"}]}},{"entity":"ClinVarVariant:13055","phenotype":{"types":[{"id":"HP:0001123","label":"Visual field defect"}]}},{"entity":"ClinVarVariant:24782","phenotype":{"types":[{"id":"HP:0004722","label":"Thickening of the glomerular basement membrane"}]}},{"entity":"ClinVarVariant:157934","phenotype":{"types":[{"id":"HP:0001433","label":"Hepatosplenomegaly"}]}},{"entity":"MGI:2150685","phenotype":{"types":[{"id":"MP:0004616","label":"lumbar vertebral transformation"}]}},{"entity":"ClinVarVariant:11962","phenotype":{"types":[{"id":"HP:0000090","label":"Nephronophthisis"}]}},{"entity":"ClinVarVariant:13394","phenotype":{"types":[{"id":"HP:0002381","label":"Aphasia"}]}},{"entity":"MGI:3574394","phenotype":{"types":[{"id":"HP:0005180","label":"Tricuspid regurgitation"}]}},{"entity":"ClinVarVariant:13369","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"AQTL:23249","phenotype":{"types":[{"id":"AQTLTrait:1252","label":"Milk myristic acid percentage"}]}},{"entity":"ClinVarVariant:42400","phenotype":{"types":[{"id":"HP:0000646","label":"Amblyopia"}]}},{"entity":"ClinVarVariant:5540","phenotype":{"types":[{"id":"HP:0100726","label":"Kaposi's sarcoma"}]}},{"entity":"MGI:3576366","phenotype":{"types":[{"id":"MP:0009503","label":"abnormal mammary gland duct morphology"}]}},{"entity":"ClinVarVariant:143094","phenotype":{"types":[{"id":"HP:0000648","label":"Optic atrophy"}]}},{"entity":"ClinVarVariant:48927","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"MGI:3580645","phenotype":{"types":[{"id":"MP:0009004","label":"progressive hair loss"}]}},{"entity":"ClinVarVariant:142003","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:56607","phenotype":{"types":[{"id":"HP:0004327","label":"Abnormality of the vitreous humor"}]}},{"entity":"ClinVarVariant:136164","phenotype":{"types":[{"id":"HP:0000825","label":"Hyperinsulinemic hypoglycemia"}]}},{"entity":"MGI:2670437","phenotype":{"types":[{"id":"MP:0000886","label":"abnormal cerebellar granule layer morphology"}]}},{"entity":"ClinVarVariant:167723","phenotype":{"types":[{"id":"HP:0002894","label":"Neoplasm of the pancreas"}]}},{"entity":"ClinVarVariant:17344","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:41212","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:209049","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"dbSNP:rs29013986","phenotype":{"types":[{"id":"AQTLTrait:1169","label":"Interval to first estrus after calving"}]}},{"entity":"ClinVarVariant:210454","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"MGI:1857966","phenotype":{"types":[{"id":"HP:0001402","label":"Hepatocellular carcinoma"}]}},{"entity":"ClinVarVariant:56243","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:208006","phenotype":{"types":[{"id":"HP:0002748","label":"Rickets"}]}},{"entity":"ClinVarVariant:139531","phenotype":{"types":[{"id":"HP:0012588","label":"Steroid-resistant nephrotic syndrome"}]}},{"entity":"ClinVarVariant:56191","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:49423","phenotype":{"types":[{"id":"HP:0009734","label":"Optic glioma"}]}},{"entity":"ClinVarVariant:11712","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:53393","phenotype":{"types":[{"id":"HP:0006530","label":"Interstitial pulmonary disease"}]}},{"entity":"FlyBase:FBal0297079","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"FlyBase:FBal0200543","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:92359","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ZFIN:ZDB-ALT-030919-2","phenotype":{"types":[{"id":"ZP:0006939","label":"abnormal(ly) has fewer parts of type spinal cord towards motor neuron"}]}},{"entity":"ClinVarVariant:216475","phenotype":{"types":[{"id":"HP:0100641","label":"Neoplasm of the adrenal cortex"}]}},{"entity":"ClinVarVariant:29874","phenotype":{"types":[{"id":"HP:0000580","label":"Pigmentary retinopathy"}]}},{"entity":"ClinVarVariant:10830","phenotype":{"types":[{"id":"HP:0003502","label":"Mild short stature"}]}},{"entity":"ClinVarVariant:95023","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:195913","phenotype":{"types":[{"id":"HP:0002342","label":"Intellectual disability, moderate"}]}},{"entity":"MGI:2387957","phenotype":{"types":[{"id":"MP:0001501","label":"abnormal sleep pattern"}]}},{"entity":"MGI:2386680","phenotype":{"types":[{"id":"GO:0042127PHENOTYPE","label":"regulation of cell proliferation phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00077732-WBRNAi00085693","phenotype":{"types":[{"id":"WBPhenotype:0001973","label":"germ cell compartment size variant"}]}},{"entity":"ClinVarVariant:135735","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008686-WBRNAi00074140","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:12403","phenotype":{"types":[{"id":"HP:0009720","label":"Adenoma sebaceum"}]}},{"entity":"MGI:5312925","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"FlyBase:FBal0202682","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:9886","phenotype":{"types":[{"id":"HP:0007984","label":"Reduced amplitude of dark-adapted bright flash electroretinogram b-wave"}]}},{"entity":"ClinVarVariant:1147","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:93888","phenotype":{"types":[{"id":"HP:0001558","label":"Decreased fetal movement"}]}},{"entity":"FlyBase:FBal0304813","phenotype":{"types":[{"id":"FBcv:0000366","label":"female sterile"}]}},{"entity":"MGI:1857056","phenotype":{"types":[{"id":"MP:0006396","label":"decreased long bone epiphyseal plate size"}]}},{"entity":"ClinVarVariant:53989","phenotype":{"types":[{"id":"HP:0000823","label":"Delayed puberty"}]}},{"entity":"ClinVarVariant:49828","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-041116-2-ZDB-MRPHLNO-150216-1-ZDB-MRPHLNO-150216-2","phenotype":{"types":[{"id":"ZP:0012064","label":"abnormal(ly) decreased occurrence adenohypophysis corticotropin hormone secreting cell differentiation"}]}},{"entity":"ClinVarVariant:2679","phenotype":{"types":[{"id":"HP:0008064","label":"Ichthyosis"}]}},{"entity":"MGI:2671317","phenotype":{"types":[{"id":"MP:0011089","label":"perinatal lethality, complete penetrance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004808-WBRNAi00072509","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"ClinVarVariant:93457","phenotype":{"types":[{"id":"HP:0001873","label":"Thrombocytopenia"}]}},{"entity":"ClinVarVariant:1563","phenotype":{"types":[{"id":"HP:0003309","label":"Ovoid thoracolumbar vertebrae"}]}},{"entity":"ClinVarVariant:159086","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"MGI:4365388","phenotype":{"types":[{"id":"MP:0009793","label":"sebaceous gland hypertrophy"}]}},{"entity":"ClinVarVariant:198219","phenotype":{"types":[{"id":"HP:0000590","label":"Progressive external ophthalmoplegia"}]}},{"entity":"dbSNP:rs110304690","phenotype":{"types":[{"id":"AQTLTrait:1101","label":"Foot angle"}]}},{"entity":"ClinVarVariant:7982","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:7141","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"AQTL:35966","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:9970","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:101176","phenotype":{"types":[{"id":"HP:0000387","label":"Absent earlobe"}]}},{"entity":"ClinVarVariant:162666","phenotype":{"types":[{"id":"HP:0011950","label":"Bronchiolitis"}]}},{"entity":"MGI:1856681","phenotype":{"types":[{"id":"MP:0002855","label":"abnormal cochlear ganglion morphology"}]}},{"entity":"ClinVarVariant:67987","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"MGI:4946645","phenotype":{"types":[{"id":"MP:0000947","label":"convulsive seizures"}]}},{"entity":"ClinVarVariant:4268","phenotype":{"types":[{"id":"HP:0004370","label":"Abnormality of temperature regulation"}]}},{"entity":"ClinVarVariant:11356","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"ClinVarVariant:4439","phenotype":{"types":[{"id":"HP:0002317","label":"Unsteady gait"}]}},{"entity":"ClinVarVariant:11002","phenotype":{"types":[{"id":"HP:0001298","label":"Encephalopathy"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002845-WBRNAi00064383","phenotype":{"types":[{"id":"WBPhenotype:0001236","label":"transgene expression increased"}]}},{"entity":"ClinVarVariant:132848","phenotype":{"types":[{"id":"HP:0000023","label":"Inguinal hernia"}]}},{"entity":"ClinVarVariant:209057","phenotype":{"types":[{"id":"HP:0002331","label":"Headache (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:10175","phenotype":{"types":[{"id":"HP:0011892","label":"Vitamin K deficiency"}]}},{"entity":"dbSNP:rs29025964","phenotype":{"types":[{"id":"AQTLTrait:1073","label":"Calving ease"}]}},{"entity":"ClinVarVariant:49552","phenotype":{"types":[{"id":"HP:0009554","label":"Projection of scalp hair onto lateral cheek"}]}},{"entity":"MGI:3578093","phenotype":{"types":[{"id":"HP:0001978","label":"Extramedullary hematopoiesis"}]}},{"entity":"_:genid1975192","phenotype":{"types":[{"id":"ZP:0004393","label":"abnormal(ly) truncated intersegmental vessel"}]}},{"entity":"ClinVarVariant:17312","phenotype":{"types":[{"id":"HP:0002659","label":"Increased susceptibility to fractures"}]}},{"entity":"ClinVarVariant:10154","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:30150","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:17324","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:216201","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:38497","phenotype":{"types":[{"id":"HP:0002017","label":"Nausea and vomiting"}]}},{"entity":"ClinVarVariant:126384","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"ClinVarVariant:13938","phenotype":{"types":[{"id":"HP:0100835","label":"Benign neoplasm of the central nervous system"}]}},{"entity":"MGI:3623342","phenotype":{"types":[{"id":"MP:0011967","label":"increased or absent threshold for auditory brainstem response"}]}},{"entity":"ClinVarVariant:188826","phenotype":{"types":[{"id":"HP:0002352","label":"Leukoencephalopathy"}]}},{"entity":"ClinVarVariant:11359","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:43167","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"AQTL:43115","phenotype":{"types":[{"id":"AQTLTrait:1112","label":"Withers height"}]}},{"entity":"MGI:5502178","phenotype":{"types":[{"id":"HP:0004313","label":"Decreased antibody level in blood"}]}},{"entity":"ClinVarVariant:24217","phenotype":{"types":[{"id":"HP:0000096","label":"Glomerulosclerosis"}]}},{"entity":"ClinVarVariant:17314","phenotype":{"types":[{"id":"HP:0002982","label":"Tibial bowing"}]}},{"entity":"ClinVarVariant:139523","phenotype":{"types":[{"id":"HP:0001480","label":"Freckling"}]}},{"entity":"ClinVarVariant:215634","phenotype":{"types":[{"id":"HP:0001017","label":"Anemic pallor"}]}},{"entity":"ClinVarVariant:210454","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:1535","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:5691","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"NCBIGene:57788","phenotype":{"types":[{"id":"HP:0006532","label":"Recurrent pneumonia"}]}},{"entity":"ClinVarVariant:10717","phenotype":{"types":[{"id":"HP:0003401","label":"Paresthesia"}]}},{"entity":"ClinVarVariant:53820","phenotype":{"types":[{"id":"HP:0100513","label":"Vitamin E deficiency"}]}},{"entity":"ClinVarVariant:189569","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"MGI:3512143","phenotype":{"types":[{"id":"HP:0003468","label":"Abnormality of the vertebrae"}]}},{"entity":"ClinVarVariant:6718","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:9581","phenotype":{"types":[{"id":"HP:0000602","label":"Ophthalmoplegia"}]}},{"entity":"ClinVarVariant:4306","phenotype":{"types":[{"id":"HP:0100787","label":"Prostate neoplasm"}]}},{"entity":"ClinVarVariant:50861","phenotype":{"types":[{"id":"HP:0003251","label":"Male infertility"}]}},{"entity":"ClinVarVariant:3408","phenotype":{"types":[{"id":"HP:0000982","label":"Palmoplantar keratoderma"}]}},{"entity":"MGI:4361197","phenotype":{"types":[{"id":"MP:0010168","label":"increased CD4-positive, CD25-positive, alpha-beta regulatory T cell number"}]}},{"entity":"_:genid1975962","phenotype":{"types":[{"id":"ZP:0001173","label":"abnormal(ly) decreased pigmentation whole organism"}]}},{"entity":"ClinVarVariant:208016","phenotype":{"types":[{"id":"HP:0002748","label":"Rickets"}]}},{"entity":"ClinVarVariant:53905","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:11586","phenotype":{"types":[{"id":"HP:0002860","label":"Squamous cell carcinoma"}]}},{"entity":"ClinVarVariant:30467","phenotype":{"types":[{"id":"HP:0002949","label":"Fused cervical vertebrae"}]}},{"entity":"ClinVarVariant:809","phenotype":{"types":[{"id":"HP:0000706","label":"Unerupted tooth"}]}},{"entity":"MGI:2183813","phenotype":{"types":[{"id":"MP:0000646","label":"enlarged adrenocortical cells"}]}},{"entity":"ClinVarVariant:64943","phenotype":{"types":[{"id":"HP:0009724","label":"Subungual fibromas"}]}},{"entity":"ClinVarVariant:3904","phenotype":{"types":[{"id":"HP:0003495","label":"GM2-ganglioside accumulation"}]}},{"entity":"MGI:3653699","phenotype":{"types":[{"id":"HP:0005048","label":"Synostosis of carpal bones"}]}},{"entity":"MGI:5559460","phenotype":{"types":[{"id":"MP:0001666","label":"abnormal intestinal absorption"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004498-WBRNAi00099563","phenotype":{"types":[{"id":"WBPhenotype:0000961","label":"pattern of transgene expression variant"}]}},{"entity":"ClinVarVariant:101394","phenotype":{"types":[{"id":"HP:0001928","label":"Abnormality of coagulation"}]}},{"entity":"ClinVarVariant:10345","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:4933","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:49479","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"ClinVarVariant:212265","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:49115","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:15234","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00012221-WBRNAi00097504","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:209067","phenotype":{"types":[{"id":"HP:0002331","label":"Headache (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:1257","phenotype":{"types":[{"id":"HP:0000926","label":"Platyspondyly"}]}},{"entity":"ClinVarVariant:36379","phenotype":{"types":[{"id":"HP:0000684","label":"Delayed eruption of teeth"}]}},{"entity":"AQTL:15392","phenotype":{"types":[{"id":"AQTLTrait:1076","label":"Gestation length"}]}},{"entity":"ClinVarVariant:92880","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:694","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"ClinVarVariant:209043","phenotype":{"types":[{"id":"HP:0001115","label":"Posterior polar cataract"}]}},{"entity":"ClinVarVariant:35838","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"ClinVarVariant:216398","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:10122","phenotype":{"types":[{"id":"HP:0100310","label":"Epidural hemorrhage"}]}},{"entity":"ClinVarVariant:17784","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"FlyBase:FBal0033446","phenotype":{"types":[{"id":"FBbt:00000004PHENOTYPE","label":"Drosophila head phenotype"}]}},{"entity":"MGI:3526165","phenotype":{"types":[{"id":"GO:0032880PHENOTYPE","label":"regulation of protein localization phenotype"}]}},{"entity":"ClinVarVariant:210447","phenotype":{"types":[{"id":"HP:0005599","label":"Hypopigmentation of hair"}]}},{"entity":"ClinVarVariant:10285","phenotype":{"types":[{"id":"HP:0001369","label":"Arthritis"}]}},{"entity":"ClinVarVariant:126394","phenotype":{"types":[{"id":"HP:0002062","label":"Morphological abnormality of the pyramidal tract"}]}},{"entity":"ClinVarVariant:9599","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"ClinVarVariant:216023","phenotype":{"types":[{"id":"HP:0000035","label":"Abnormality of the testis"}]}},{"entity":"ClinVarVariant:10738","phenotype":{"types":[{"id":"HP:0000763","label":"Sensory neuropathy"}]}},{"entity":"ClinVarVariant:3571","phenotype":{"types":[{"id":"HP:0010044","label":"Short 4th metacarpal"}]}},{"entity":"ClinVarVariant:67881","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:8710","phenotype":{"types":[{"id":"HP:0002823","label":"Abnormality of the femur"}]}},{"entity":"ClinVarVariant:159228","phenotype":{"types":[{"id":"HP:0001557","label":"Prenatal movement abnormality"}]}},{"entity":"ClinVarVariant:36081","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:161334","phenotype":{"types":[{"id":"HP:0005293","label":"Venous insufficiency"}]}},{"entity":"MGI:3762530","phenotype":{"types":[{"id":"MP:0002020","label":"increased tumor incidence"}]}},{"entity":"ClinVarVariant:188302","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:11342","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"ClinVarVariant:10751","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:53923","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"MGI:5320577","phenotype":{"types":[{"id":"MP:0006059","label":"decreased susceptibility to ischemic brain injury"}]}},{"entity":"ClinVarVariant:17332","phenotype":{"types":[{"id":"HP:0002659","label":"Increased susceptibility to fractures"}]}},{"entity":"ClinVarVariant:66101","phenotype":{"types":[{"id":"HP:0011109","label":"Chronic sinusitis"}]}},{"entity":"ClinVarVariant:11596","phenotype":{"types":[{"id":"HP:0002860","label":"Squamous cell carcinoma"}]}},{"entity":"ClinVarVariant:13848","phenotype":{"types":[{"id":"HP:0007542","label":"Absent pigmentation of the ventral chest"}]}},{"entity":"ClinVarVariant:209019","phenotype":{"types":[{"id":"HP:0000777","label":"Abnormality of the thymus"}]}},{"entity":"ClinVarVariant:166927","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"AQTL:4620","phenotype":{"types":[{"id":"AQTLTrait:1099","label":"Milking speed"}]}},{"entity":"ClinVarVariant:53677","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:159171","phenotype":{"types":[{"id":"HP:0000160","label":"Narrow mouth"}]}},{"entity":"ClinVarVariant:17976","phenotype":{"types":[{"id":"HP:0006530","label":"Interstitial pulmonary disease"}]}},{"entity":"ClinVarVariant:39444","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:96580","phenotype":{"types":[{"id":"HP:0002179","label":"Opisthotonus"}]}},{"entity":"MGI:1856097","phenotype":{"types":[{"id":"MP:0010908","label":"dilated pulmonary alveolar ducts"}]}},{"entity":"ClinVarVariant:7314","phenotype":{"types":[{"id":"HP:0000678","label":"Dental crowding"}]}},{"entity":"ClinVarVariant:158904","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:215720","phenotype":{"types":[{"id":"HP:0100697","label":"Neurofibrosarcoma"}]}},{"entity":"MGI:2384515","phenotype":{"types":[{"id":"MP:0001405","label":"impaired coordination"}]}},{"entity":"MGI:3576024","phenotype":{"types":[{"id":"HP:0000157","label":"Abnormality of the tongue"}]}},{"entity":"ClinVarVariant:21535","phenotype":{"types":[{"id":"HP:0001256","label":"Intellectual disability, mild"}]}},{"entity":"ClinVarVariant:192298","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"ClinVarVariant:215688","phenotype":{"types":[{"id":"HP:0003468","label":"Abnormality of the vertebrae"}]}},{"entity":"dbSNP:rs110801629","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ZFIN:ZDB-ALT-980203-452","phenotype":{"types":[{"id":"ZP:0000148","label":"abnormal(ly) increased width notochord"}]}},{"entity":"ClinVarVariant:209053","phenotype":{"types":[{"id":"HP:0001648","label":"Cor pulmonale"}]}},{"entity":"ClinVarVariant:30527","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ZFIN:ZDB-ALT-020422-8","phenotype":{"types":[{"id":"ZP:0002275","label":"abnormal(ly) necrotic trunk"}]}},{"entity":"ClinVarVariant:10249","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:101204","phenotype":{"types":[{"id":"HP:0010318","label":"Aplasia/Hypoplasia of the abdominal wall musculature"}]}},{"entity":"ClinVarVariant:9956","phenotype":{"types":[{"id":"HP:0001923","label":"Reticulocytosis"}]}},{"entity":"ClinVarVariant:126447","phenotype":{"types":[{"id":"HP:0100689","label":"Decreased corneal thickness"}]}},{"entity":"ClinVarVariant:93336","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:36957","phenotype":{"types":[{"id":"HP:0001539","label":"Omphalocele"}]}},{"entity":"ClinVarVariant:190118","phenotype":{"types":[{"id":"HP:0002015","label":"Dysphagia"}]}},{"entity":"ClinVarVariant:210474","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:159234","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:40522","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:605","phenotype":{"types":[{"id":"HP:0004923","label":"Hyperphenylalaninemia"}]}},{"entity":"MGI:2155766","phenotype":{"types":[{"id":"MP:0002836","label":"abnormal chorion morphology"}]}},{"entity":"MGI:3511363","phenotype":{"types":[{"id":"HP:0001539","label":"Omphalocele"}]}},{"entity":"ClinVarVariant:41344","phenotype":{"types":[{"id":"HP:0007067","label":"Distal peripheral sensory neuropathy"}]}},{"entity":"ClinVarVariant:38578","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"MGI:4842477","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:82347","phenotype":{"types":[{"id":"HP:0006753","label":"Neoplasm of the stomach"}]}},{"entity":"MGI:1856222","phenotype":{"types":[{"id":"MP:0002938","label":"white spotting"}]}},{"entity":"ClinVarVariant:49718","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"MGI:2652711","phenotype":{"types":[{"id":"MP:0011750","label":"abnormal seminiferous tubule epithelium morphology"}]}},{"entity":"MGI:3056917","phenotype":{"types":[{"id":"MP:0001402","label":"hypoactivity"}]}},{"entity":"MGI:2158307","phenotype":{"types":[{"id":"MP:0002722","label":"abnormal immune system organ morphology"}]}},{"entity":"ClinVarVariant:40526","phenotype":{"types":[{"id":"HP:0000520","label":"Proptosis"}]}},{"entity":"ClinVarVariant:41247","phenotype":{"types":[{"id":"HP:0003429","label":"CNS hypomyelination"}]}},{"entity":"ClinVarVariant:53618","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"FlyBase:FBal0207560","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:216725","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:158962","phenotype":{"types":[{"id":"HP:0011308","label":"Slender toe"}]}},{"entity":"MGI:4880750","phenotype":{"types":[{"id":"MP:0008702","label":"increased interleukin-5 secretion"}]}},{"entity":"AQTL:23951","phenotype":{"types":[{"id":"AQTLTrait:1196","label":"Abomasum displacement"}]}},{"entity":"MGI:1929775","phenotype":{"types":[{"id":"MP:0008148","label":"abnormal rib-sternum attachment"}]}},{"entity":"ClinVarVariant:53716","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:36083","phenotype":{"types":[{"id":"HP:0000767","label":"Pectus excavatum"}]}},{"entity":"ClinVarVariant:88836","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:35713","phenotype":{"types":[{"id":"HP:0000934","label":"Chondrocalcinosis"}]}},{"entity":"ClinVarVariant:190232","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"ClinVarVariant:190368","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:156281","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:210008","phenotype":{"types":[{"id":"HP:0002301","label":"Hemiplegia"}]}},{"entity":"ClinVarVariant:56669","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:8259","phenotype":{"types":[{"id":"HP:0001056","label":"Milia"}]}},{"entity":"ClinVarVariant:10619","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:135769","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:25004","phenotype":{"types":[{"id":"HP:0007703","label":"Abnormality of retinal pigmentation"}]}},{"entity":"MGI:1856699","phenotype":{"types":[{"id":"MP:0001212","label":"skin lesions"}]}},{"entity":"ClinVarVariant:10217","phenotype":{"types":[{"id":"HP:0011892","label":"Vitamin K deficiency"}]}},{"entity":"ClinVarVariant:60779","phenotype":{"types":[{"id":"HP:0008180","label":"Mildly elevated creatine phosphokinase"}]}},{"entity":"ClinVarVariant:53779","phenotype":{"types":[{"id":"HP:0100660","label":"Dyskinesia"}]}},{"entity":"ClinVarVariant:24687","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:100728","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ClinVarVariant:156381","phenotype":{"types":[{"id":"HP:0000365","label":"Hearing impairment"}]}},{"entity":"ClinVarVariant:41692","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"FlyBase:FBal0126487","phenotype":{"types":[{"id":"FBbt:00001682PHENOTYPE","label":"Drosophila embryonic/larval hemocoel phenotype"}]}},{"entity":"ClinVarVariant:52398","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006700-WBRNAi00061477","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"ClinVarVariant:183367","phenotype":{"types":[{"id":"HP:0005218","label":"Anoperineal fistula"}]}},{"entity":"ClinVarVariant:2482","phenotype":{"types":[{"id":"HP:0001608","label":"Abnormality of the voice"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001892-WBRNAi00025035","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:42345","phenotype":{"types":[{"id":"HP:0004933","label":"Ascending aortic dissection"}]}},{"entity":"ClinVarVariant:9983","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:21565","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:5633","phenotype":{"types":[{"id":"HP:0000141","label":"Amenorrhea"}]}},{"entity":"ClinVarVariant:16624","phenotype":{"types":[{"id":"HP:0003762","label":"Uterus didelphys"}]}},{"entity":"ClinVarVariant:181715","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:199203","phenotype":{"types":[{"id":"HP:0002486","label":"Myotonia"}]}},{"entity":"ClinVarVariant:53715","phenotype":{"types":[{"id":"HP:0004936","label":"Venous thrombosis"}]}},{"entity":"ClinVarVariant:209059","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:56253","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:14091","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:12493","phenotype":{"types":[{"id":"HP:0001944","label":"Dehydration"}]}},{"entity":"MGI:5468098","phenotype":{"types":[{"id":"HP:0011849","label":"Abnormal bone ossification"}]}},{"entity":"MGI:5443922","phenotype":{"types":[{"id":"HP:0003233","label":"Hypoalphalipoproteinemia"}]}},{"entity":"ClinVarVariant:207574","phenotype":{"types":[{"id":"HP:0002495","label":"Impaired vibratory sensation"}]}},{"entity":"WormBase:WBVar00242117","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:53226","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:11430","phenotype":{"types":[{"id":"HP:0008839","label":"Hypoplastic pelvis"}]}},{"entity":"ClinVarVariant:10058","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"ClinVarVariant:158385","phenotype":{"types":[{"id":"HP:0000717","label":"Autism"}]}},{"entity":"MGI:5141269","phenotype":{"types":[{"id":"HP:0002591","label":"Polyphagia"}]}},{"entity":"ClinVarVariant:181494","phenotype":{"types":[{"id":"HP:0010541","label":"Cutis gyrata of scalp"}]}},{"entity":"ClinVarVariant:12391","phenotype":{"types":[{"id":"HP:0011364","label":"White hair"}]}},{"entity":"ClinVarVariant:53911","phenotype":{"types":[{"id":"HP:0003453","label":"Antineutrophil antibody positivity"}]}},{"entity":"MGI:2151589","phenotype":{"types":[{"id":"MP:0009355","label":"increased liver triglyceride level"}]}},{"entity":"ClinVarVariant:38415","phenotype":{"types":[{"id":"HP:0003264","label":"Deficiency of N-acetylglucosamine-1-phosphotransferase"}]}},{"entity":"ClinVarVariant:30832","phenotype":{"types":[{"id":"HP:0100790","label":"Hernia"}]}},{"entity":"FlyBase:FBal0209815","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:180622","phenotype":{"types":[{"id":"HP:0004430","label":"Severe combined immunodeficiency"}]}},{"entity":"ClinVarVariant:24371","phenotype":{"types":[{"id":"HP:0000958","label":"Dry skin"}]}},{"entity":"ClinVarVariant:156327","phenotype":{"types":[{"id":"HP:0100512","label":"Vitamin D deficiency"}]}},{"entity":"ClinVarVariant:54054","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:197080","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"MGI:4358721","phenotype":{"types":[{"id":"MP:0001523","label":"impaired righting response"}]}},{"entity":"ClinVarVariant:199965","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"ClinVarVariant:29","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"MGI:3623117","phenotype":{"types":[{"id":"MP:0004918","label":"abnormal negative T cell selection"}]}},{"entity":"ClinVarVariant:158914","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:30626","phenotype":{"types":[{"id":"HP:0100532","label":"Scleritis"}]}},{"entity":"ClinVarVariant:53187","phenotype":{"types":[{"id":"HP:0011968","label":"Feeding difficulties"}]}},{"entity":"FlyBase:FBal0043110","phenotype":{"types":[{"id":"FBbt:00000169PHENOTYPE","label":"embryonic mesothoracic segment phenotype"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017282-WBRNAi00102984","phenotype":{"types":[{"id":"WBPhenotype:0000462","label":"paraquat hypersensitive"}]}},{"entity":"ClinVarVariant:53320","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"MGI:3639295","phenotype":{"types":[{"id":"HP:0011121","label":"Abnormality of skin morphology"}]}},{"entity":"ClinVarVariant:215752","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"ClinVarVariant:215780","phenotype":{"types":[{"id":"HP:0003241","label":"External genital hypoplasia"}]}},{"entity":"ClinVarVariant:91650","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:55948","phenotype":{"types":[{"id":"HP:0006887","label":"Intellectual disability, progressive"}]}},{"entity":"ClinVarVariant:17209","phenotype":{"types":[{"id":"HP:0000973","label":"Cutis laxa"}]}},{"entity":"ClinVarVariant:1461","phenotype":{"types":[{"id":"HP:0006597","label":"Diaphragmatic paralysis"}]}},{"entity":"ClinVarVariant:4310","phenotype":{"types":[{"id":"HP:0003540","label":"Impaired platelet aggregation"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00194986-WBRNAi00085581","phenotype":{"types":[{"id":"WBPhenotype:0001951","label":"pachytene region organization variant"}]}},{"entity":"ClinVarVariant:5069","phenotype":{"types":[{"id":"HP:0100716","label":"Self-injurious behavior"}]}},{"entity":"ClinVarVariant:11644","phenotype":{"types":[{"id":"HP:0000395","label":"Prominent antihelix"}]}},{"entity":"ClinVarVariant:210461","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:217066","phenotype":{"types":[{"id":"HP:0009736","label":"Tibial pseudoarthrosis"}]}},{"entity":"ClinVarVariant:41306","phenotype":{"types":[{"id":"HP:0011449","label":"Knee clonus"}]}},{"entity":"ClinVarVariant:216230","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:16085","phenotype":{"types":[{"id":"HP:0007495","label":"Prematurely aged appearance"}]}},{"entity":"MGI:3785252","phenotype":{"types":[{"id":"MP:0008874","label":"decreased physiological sensitivity to xenobiotic"}]}},{"entity":"_:genid1975900","phenotype":{"types":[{"id":"ZP:0000038","label":"abnormal(ly) edematous pericardium"}]}},{"entity":"ClinVarVariant:11540","phenotype":{"types":[{"id":"HP:0002007","label":"Frontal bossing"}]}},{"entity":"MGI:3624263","phenotype":{"types":[{"id":"MP:0011186","label":"abnormal visceral endoderm morphology"}]}},{"entity":"ClinVarVariant:53939","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ClinVarVariant:156552","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"ClinVarVariant:24978","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:41131","phenotype":{"types":[{"id":"HP:0000252","label":"Microcephaly"}]}},{"entity":"ClinVarVariant:36033","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"FlyBase:FBal0210612","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:2149","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ClinVarVariant:24396","phenotype":{"types":[{"id":"HP:0008063","label":"Aplasia/Hypoplasia of the lens"}]}},{"entity":"ClinVarVariant:24651","phenotype":{"types":[{"id":"HP:0011501","label":"Anterior lenticonus"}]}},{"entity":"ClinVarVariant:24375","phenotype":{"types":[{"id":"HP:0000093","label":"Proteinuria"}]}},{"entity":"ClinVarVariant:25310","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:40502","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"ClinVarVariant:167188","phenotype":{"types":[{"id":"HP:0000470","label":"Short neck"}]}},{"entity":"ClinVarVariant:2128","phenotype":{"types":[{"id":"HP:0000612","label":"Iris coloboma"}]}},{"entity":"MGI:2385717","phenotype":{"types":[{"id":"MP:0002961","label":"abnormal axon guidance"}]}},{"entity":"MGI:2683050","phenotype":{"types":[{"id":"HP:0004324","label":"Increased body weight"}]}},{"entity":"ClinVarVariant:50055","phenotype":{"types":[{"id":"HP:0009716","label":"Subependymal nodules"}]}},{"entity":"ClinVarVariant:7853","phenotype":{"types":[{"id":"HP:0001289","label":"Confusion"}]}},{"entity":"ClinVarVariant:142534","phenotype":{"types":[{"id":"HP:0001562","label":"Oligohydramnios"}]}},{"entity":"MGI:5470094","phenotype":{"types":[{"id":"HP:0002450","label":"Abnormal motor neuron morphology"}]}},{"entity":"MGI:5441311","phenotype":{"types":[{"id":"MP:0009763","label":"increased sensitivity to induced morbidity/mortality"}]}},{"entity":"MGI:5007063","phenotype":{"types":[{"id":"MP:0002116","label":"abnormal craniofacial bone morphology"}]}},{"entity":"ClinVarVariant:188088","phenotype":{"types":[{"id":"HP:0002669","label":"Osteosarcoma"}]}},{"entity":"ClinVarVariant:196277","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:38289","phenotype":{"types":[{"id":"HP:0002789","label":"Tachypnea"}]}},{"entity":"ClinVarVariant:16741","phenotype":{"types":[{"id":"HP:0000153","label":"Abnormality of the mouth"}]}},{"entity":"ClinVarVariant:10654","phenotype":{"types":[{"id":"HP:0003237","label":"Increased IgG level"}]}},{"entity":"ClinVarVariant:5508","phenotype":{"types":[{"id":"HP:0000882","label":"Hypoplastic scapulae"}]}},{"entity":"ClinVarVariant:211503","phenotype":{"types":[{"id":"HP:0001195","label":"Single umbilical artery"}]}},{"entity":"ClinVarVariant:53915","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:3756","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:42443","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"MGI:3798768","phenotype":{"types":[{"id":"MP:0005076","label":"abnormal cell differentiation"}]}},{"entity":"ClinVarVariant:101503","phenotype":{"types":[{"id":"HP:0010752","label":"Cleft mandible"}]}},{"entity":"ClinVarVariant:64997","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:1539","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:101108","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"ClinVarVariant:43202","phenotype":{"types":[{"id":"HP:0000360","label":"Tinnitus"}]}},{"entity":"ClinVarVariant:5943","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:24508","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:38311","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:1128","phenotype":{"types":[{"id":"HP:0000895","label":"Lateral clavicle hook"}]}},{"entity":"MGI:2388126","phenotype":{"types":[{"id":"MP:0002113","label":"abnormal skeleton development"}]}},{"entity":"ClinVarVariant:96576","phenotype":{"types":[{"id":"HP:0008872","label":"Feeding difficulties in infancy"}]}},{"entity":"ClinVarVariant:53236","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:193747","phenotype":{"types":[{"id":"HP:0001256","label":"Intellectual disability, mild"}]}},{"entity":"ClinVarVariant:126412","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:94109","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"dbSNP:rs41666553","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:31217","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:54003","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:25350","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"ClinVarVariant:198365","phenotype":{"types":[{"id":"HP:0000518","label":"Cataract"}]}},{"entity":"ClinVarVariant:24676","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"ClinVarVariant:94210","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:101296","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"DOID:11726","phenotype":{"types":[{"id":"HP:0001638","label":"Cardiomyopathy"}]}},{"entity":"FlyBase:FBal0118076","phenotype":{"types":[{"id":"FBcv:0000394","label":"circadian rhythm defective"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00009186-WBRNAi00045737","phenotype":{"types":[{"id":"WBPhenotype:0000640","label":"egg laying variant"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003186-WBRNAi00085575","phenotype":{"types":[{"id":"WBPhenotype:0000291","label":"no oocytes"}]}},{"entity":"ClinVarVariant:24755","phenotype":{"types":[{"id":"HP:0000488","label":"Retinopathy"}]}},{"entity":"ClinVarVariant:11836","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:158924","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:67977","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:55823","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050523-1-ZDB-MRPHLNO-080703-4","phenotype":{"types":[{"id":"ZP:0007823","label":"abnormal(ly) increased width floor plate rhombomere region"}]}},{"entity":"ClinVarVariant:65018","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:67936","phenotype":{"types":[{"id":"HP:0001645","label":"Sudden cardiac death"}]}},{"entity":"ClinVarVariant:188997","phenotype":{"types":[{"id":"HP:0001954","label":"Episodic fever"}]}},{"entity":"ClinVarVariant:190776","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:50061","phenotype":{"types":[{"id":"HP:0000269","label":"Prominent occiput"}]}},{"entity":"ClinVarVariant:13674","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-030131-180-ZDB-MRPHLNO-110715-2","phenotype":{"types":[{"id":"GO:0035188PHENOTYPE","label":"hatching phenotype"}]}},{"entity":"ClinVarVariant:6639","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"FlyBase:FBal0205870","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"ClinVarVariant:54073","phenotype":{"types":[{"id":"HP:0000966","label":"Hypohidrosis"}]}},{"entity":"MGI:3588578","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:50112","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"ClinVarVariant:11860","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008688-WBRNAi00080126","phenotype":{"types":[{"id":"ZP:0000676","label":"abnormal(ly) increased rate cell proliferation"}]}},{"entity":"ClinVarVariant:18086","phenotype":{"types":[{"id":"HP:0002884","label":"Hepatoblastoma"}]}},{"entity":"ClinVarVariant:7516","phenotype":{"types":[{"id":"HP:0010864","label":"Intellectual disability, severe"}]}},{"entity":"ClinVarVariant:94475","phenotype":{"types":[{"id":"HP:0002948","label":"Vertebral fusion"}]}},{"entity":"dbSNP:rs12793173","phenotype":{"types":[{"id":"HP:0000969","label":"Edema"}]}},{"entity":"ClinVarVariant:1532","phenotype":{"types":[{"id":"HP:0010980","label":"Hyperlipoproteinemia"}]}},{"entity":"ClinVarVariant:158567","phenotype":{"types":[{"id":"HP:0009836","label":"Broad distal phalanx of finger"}]}},{"entity":"ClinVarVariant:188263","phenotype":{"types":[{"id":"HP:0002321","label":"Vertigo"}]}},{"entity":"ClinVarVariant:141451","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00015583-WBRNAi00077058","phenotype":{"types":[{"id":"WBPhenotype:0000012","label":"dauer constitutive"}]}},{"entity":"ClinVarVariant:208075","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"MGI:2156546","phenotype":{"types":[{"id":"MP:0005597","label":"decreased susceptibility to type I hypersensitivity reaction"}]}},{"entity":"MGI:5285080","phenotype":{"types":[{"id":"MP:0013209","label":"abnormal motile cilium physiology"}]}},{"entity":"ClinVarVariant:38281","phenotype":{"types":[{"id":"HP:0011131","label":"Perianal rash"}]}},{"entity":"ClinVarVariant:53127","phenotype":{"types":[{"id":"HP:0006696","label":"Polymorphic and polytopic ventricular extrasystoles"}]}},{"entity":"MGI:3822156","phenotype":{"types":[{"id":"MP:0000281","label":"abnormal interventricular septum morphology"}]}},{"entity":"ClinVarVariant:49660","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:39711","phenotype":{"types":[{"id":"HP:0001171","label":"Split hand"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003947-WBRNAi00085486","phenotype":{"types":[{"id":"WBPhenotype:0001950","label":"diplotene region organization variant"}]}},{"entity":"ClinVarVariant:127405","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:43995","phenotype":{"types":[{"id":"HP:0001678","label":"Atrioventricular block"}]}},{"entity":"ClinVarVariant:188886","phenotype":{"types":[{"id":"HP:0001878","label":"Hemolytic anemia"}]}},{"entity":"ClinVarVariant:101248","phenotype":{"types":[{"id":"HP:0100627","label":"Displacement of the external urethral meatus"}]}},{"entity":"ClinVarVariant:17360","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006375-WBRNAi00097656","phenotype":{"types":[{"id":"ZP:0004962","label":"abnormal(ly) increased rate apoptotic process"}]}},{"entity":"ClinVarVariant:38942","phenotype":{"types":[{"id":"HP:0001399","label":"Hepatic failure"}]}},{"entity":"ClinVarVariant:8482","phenotype":{"types":[{"id":"HP:0001332","label":"Dystonia"}]}},{"entity":"ClinVarVariant:12497","phenotype":{"types":[{"id":"HP:0011039","label":"Abnormality of the helix"}]}},{"entity":"ClinVarVariant:1480","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:189710","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:690","phenotype":{"types":[{"id":"HP:0000914","label":"Shield chest"}]}},{"entity":"ClinVarVariant:136123","phenotype":{"types":[{"id":"HP:0000980","label":"Pallor"}]}},{"entity":"MGI:3040471","phenotype":{"types":[{"id":"HP:0011111","label":"Abnormality of immune serum protein physiology"}]}},{"entity":"ClinVarVariant:210716","phenotype":{"types":[{"id":"HP:0001231","label":"Abnormality of the fingernails"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001967-WBRNAi00070035","phenotype":{"types":[{"id":"WBPhenotype:0000696","label":"everted vulva"}]}},{"entity":"ClinVarVariant:53210","phenotype":{"types":[{"id":"HP:0006536","label":"Obstructive lung disease"}]}},{"entity":"ClinVarVariant:53246","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:24716","phenotype":{"types":[{"id":"HP:0012211","label":"Abnormal renal physiology"}]}},{"entity":"ClinVarVariant:212636","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:10118","phenotype":{"types":[{"id":"HP:0001342","label":"Cerebral hemorrhage"}]}},{"entity":"ClinVarVariant:17484","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"ClinVarVariant:202177","phenotype":{"types":[{"id":"HP:0010780","label":"Hyperacusis"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-050419-261-ZDB-MRPHLNO-130117-3","phenotype":{"types":[{"id":"ZP:0002516","label":"abnormal(ly) cystic pronephric glomerulus"}]}},{"entity":"ClinVarVariant:66036","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"dbSNP:rs586716","phenotype":{"types":[{"id":"HP:0003418","label":"Back pain"}]}},{"entity":"ClinVarVariant:101414","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:49414","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"ClinVarVariant:166862","phenotype":{"types":[{"id":"HP:0000689","label":"Dental malocclusion"}]}},{"entity":"ClinVarVariant:41344","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"MGI:5431878","phenotype":{"types":[{"id":"HP:0012373","label":"Abnormal eye physiology"}]}},{"entity":"ClinVarVariant:155889","phenotype":{"types":[{"id":"HP:0001950","label":"Respiratory alkalosis"}]}},{"entity":"ClinVarVariant:1743","phenotype":{"types":[{"id":"HP:0200118","label":"Malabsorption of Vitamin B12"}]}},{"entity":"ClinVarVariant:65028","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:24275","phenotype":{"types":[{"id":"HP:0000100","label":"Nephrotic syndrome"}]}},{"entity":"ClinVarVariant:53680","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:92800","phenotype":{"types":[{"id":"HP:0000219","label":"Thin upper lip vermilion"}]}},{"entity":"ClinVarVariant:13997","phenotype":{"types":[{"id":"HP:0004429","label":"Recurrent viral infections"}]}},{"entity":"ClinVarVariant:54064","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"MGI:1857348","phenotype":{"types":[{"id":"HP:0100495","label":"Mastocytosis"}]}},{"entity":"ClinVarVariant:40512","phenotype":{"types":[{"id":"HP:0000276","label":"Long face"}]}},{"entity":"FlyBase:FBal0095694","phenotype":{"types":[{"id":"FBbt:00004200PHENOTYPE","label":"retina phenotype"}]}},{"entity":"MGI:2677682","phenotype":{"types":[{"id":"MP:0002813","label":"microcytosis"}]}},{"entity":"dbSNP:rs7045640","phenotype":{"types":[{"id":"HP:0001489","label":"Posterior vitreous detachment"}]}},{"entity":"ClinVarVariant:5094","phenotype":{"types":[{"id":"HP:0002757","label":"Recurrent fractures"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002064-WBRNAi00063098","phenotype":{"types":[{"id":"WBPhenotype:0000291","label":"no oocytes"}]}},{"entity":"ClinVarVariant:11134","phenotype":{"types":[{"id":"HP:0001891","label":"Iron deficiency anemia"}]}},{"entity":"ClinVarVariant:189284","phenotype":{"types":[{"id":"HP:0008572","label":"External ear malformation"}]}},{"entity":"MGI:3057163","phenotype":{"types":[{"id":"HP:0001882","label":"Leukopenia"}]}},{"entity":"MGI:3846101","phenotype":{"types":[{"id":"MP:0002874","label":"decreased hemoglobin content"}]}},{"entity":"ClinVarVariant:12051","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:56263","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"AQTL:11570","phenotype":{"types":[{"id":"AQTLTrait:224","label":"Small intestinal Escherichia coli F18 receptor"}]}},{"entity":"ClinVarVariant:40551","phenotype":{"types":[{"id":"HP:0010541","label":"Cutis gyrata of scalp"}]}},{"entity":"ClinVarVariant:54031","phenotype":{"types":[{"id":"HP:0005948","label":"Cystic lung disease"}]}},{"entity":"ClinVarVariant:42343","phenotype":{"types":[{"id":"HP:0000494","label":"Downslanted palpebral fissures"}]}},{"entity":"MGI:3512077","phenotype":{"types":[{"id":"MP:0000750","label":"abnormal muscle regeneration"}]}},{"entity":"ClinVarVariant:50982","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"MGI:2448247","phenotype":{"types":[{"id":"MP:0001176","label":"abnormal lung development"}]}},{"entity":"ClinVarVariant:53871","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004078-WBRNAi00091973","phenotype":{"types":[{"id":"ZP:0000305","label":"abnormal(ly) arrested embryo development"}]}},{"entity":"FlyBase:FBal0200222","phenotype":{"types":[{"id":"FBbt:00005149PHENOTYPE","label":"ganglion mother cell phenotype"}]}},{"entity":"ClinVarVariant:216429","phenotype":{"types":[{"id":"HP:0100280","label":"Crohn's disease"}]}},{"entity":"ClinVarVariant:2392","phenotype":{"types":[{"id":"HP:0003218","label":"Oroticaciduria"}]}},{"entity":"ClinVarVariant:142966","phenotype":{"types":[{"id":"HP:0000777","label":"Abnormality of the thymus"}]}},{"entity":"MGI:3624543","phenotype":{"types":[{"id":"MP:0000951","label":"sporadic seizures"}]}},{"entity":"ClinVarVariant:133608","phenotype":{"types":[{"id":"HP:0002344","label":"Progressive neurologic deterioration"}]}},{"entity":"ClinVarVariant:211626","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:9656","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:25215","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:10572","phenotype":{"types":[{"id":"HP:0005186","label":"Synovial hypertrophy"}]}},{"entity":"MGI:3722688","phenotype":{"types":[{"id":"HP:0003022","label":"Hypoplasia of the ulna"}]}},{"entity":"ClinVarVariant:93129","phenotype":{"types":[{"id":"HP:0002371","label":"Loss of speech"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004806-WBRNAi00036044","phenotype":{"types":[{"id":"ZP:0003666","label":"abnormal(ly) arrested larval development"}]}},{"entity":"MGI:2386742","phenotype":{"types":[{"id":"HP:0001719","label":"Double outlet right ventricle"}]}},{"entity":"ClinVarVariant:12534","phenotype":{"types":[{"id":"HP:0002659","label":"Increased susceptibility to fractures"}]}},{"entity":"ClinVarVariant:53491","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"WormBase:WBVar00087758","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:100772","phenotype":{"types":[{"id":"HP:0000174","label":"Abnormality of the palate"}]}},{"entity":"FlyBase:FBal0269186","phenotype":{"types":[{"id":"FBbt:00004646PHENOTYPE","label":"tarsal segment phenotype"}]}},{"entity":"ClinVarVariant:209167","phenotype":{"types":[{"id":"HP:0000666","label":"Horizontal nystagmus"}]}},{"entity":"AQTL:29399","phenotype":{"types":[{"id":"AQTLTrait:1085","label":"Degree of Spotting"}]}},{"entity":"ZFIN:ZDB-ALT-090611-2","phenotype":{"types":[{"id":"GO:0045765PHENOTYPE","label":"regulation of angiogenesis phenotype"}]}},{"entity":"ClinVarVariant:36053","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:101388","phenotype":{"types":[{"id":"HP:0009906","label":"Aplasia/Hypoplasia of the earlobes"}]}},{"entity":"MGI:3605473","phenotype":{"types":[{"id":"MP:0004167","label":"abnormal cingulate gyrus morphology"}]}},{"entity":"MGI:4433578","phenotype":{"types":[{"id":"MP:0004527","label":"abnormal outer hair cell stereociliary bundle morphology"}]}},{"entity":"ClinVarVariant:2324","phenotype":{"types":[{"id":"HP:0001315","label":"Reduced tendon reflexes"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-061103-265-ZDB-MRPHLNO-140606-7","phenotype":{"types":[{"id":"ZP:0004552","label":"abnormal(ly) bilateral symmetry heart tube"}]}},{"entity":"ClinVarVariant:181833","phenotype":{"types":[{"id":"HP:0100777","label":"Exostoses"}]}},{"entity":"ClinVarVariant:93455","phenotype":{"types":[{"id":"HP:0000939","label":"Osteoporosis"}]}},{"entity":"MGI:3817754","phenotype":{"types":[{"id":"HP:0000859","label":"Hyperaldosteronism"}]}},{"entity":"ClinVarVariant:211657","phenotype":{"types":[{"id":"HP:0000776","label":"Congenital diaphragmatic hernia"}]}},{"entity":"ClinVarVariant:35972","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:4674","phenotype":{"types":[{"id":"HP:0000989","label":"Pruritus"}]}},{"entity":"ClinVarVariant:8953","phenotype":{"types":[{"id":"HP:0006380","label":"Knee flexion contracture"}]}},{"entity":"FlyBase:FBal0221490","phenotype":{"types":[{"id":"FBbt:00004483PHENOTYPE","label":"Drosophila ptilinum phenotype"}]}},{"entity":"FlyBase:FBal0050220","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"FlyBase:FBal0200679","phenotype":{"types":[{"id":"FBcv:0000354","label":"visible"}]}},{"entity":"MGI:2178387","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:41120","phenotype":{"types":[{"id":"HP:0100612","label":"Odontogenic neoplasm"}]}},{"entity":"ClinVarVariant:13723","phenotype":{"types":[{"id":"HP:0001259","label":"Coma"}]}},{"entity":"ClinVarVariant:161333","phenotype":{"types":[{"id":"HP:0001038","label":"Warfarin-induced skin necrosis"}]}},{"entity":"ClinVarVariant:6099","phenotype":{"types":[{"id":"HP:0003312","label":"Abnormal form of the vertebral bodies"}]}},{"entity":"ClinVarVariant:41180","phenotype":{"types":[{"id":"HP:0000421","label":"Epistaxis"}]}},{"entity":"ClinVarVariant:9430","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:99932","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:36072","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:1987","phenotype":{"types":[{"id":"HP:0000057","label":"obsolete Clitoromegaly"}]}},{"entity":"ClinVarVariant:158899","phenotype":{"types":[{"id":"HP:0003324","label":"Generalized muscle weakness"}]}},{"entity":"ZFIN:ZDB-ALT-041008-4","phenotype":{"types":[{"id":"ZP:0000407","label":"abnormal(ly) decreased width head"}]}},{"entity":"ClinVarVariant:7292","phenotype":{"types":[{"id":"HP:0001053","label":"Hypopigmented skin patches"}]}},{"entity":"ClinVarVariant:67378","phenotype":{"types":[{"id":"HP:0000407","label":"Sensorineural hearing impairment"}]}},{"entity":"ClinVarVariant:36284","phenotype":{"types":[{"id":"HP:0000832","label":"Primary hypothyroidism"}]}},{"entity":"ClinVarVariant:194096","phenotype":{"types":[{"id":"HP:0000572","label":"Visual loss"}]}},{"entity":"ClinVarVariant:197503","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"AQTL:15249","phenotype":{"types":[{"id":"AQTLTrait:1027","label":"Marbling score"}]}},{"entity":"ClinVarVariant:49120","phenotype":{"types":[{"id":"HP:0008696","label":"Renal hamartoma"}]}},{"entity":"ClinVarVariant:12335","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:7979","phenotype":{"types":[{"id":"HP:0000400","label":"Macrotia"}]}},{"entity":"ClinVarVariant:49153","phenotype":{"types":[{"id":"HP:0000821","label":"Hypothyroidism"}]}},{"entity":"ClinVarVariant:53913","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:133623","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ZFIN:ZDB-ALT-100723-4","phenotype":{"types":[{"id":"ZP:0007051","label":"abnormal(ly) dilated melanocyte"}]}},{"entity":"ClinVarVariant:88731","phenotype":{"types":[{"id":"HP:0012557","label":"EEG with centrotemporal focal spike waves"}]}},{"entity":"ClinVarVariant:49298","phenotype":{"types":[{"id":"HP:0009727","label":"Achromatic retinal patches"}]}},{"entity":"dbSNP:rs136851063","phenotype":{"types":[{"id":"AQTLTrait:1327","label":"Milk odd-chain fatty acid percentage"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00012059-WBRNAi00009225","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:30201","phenotype":{"types":[{"id":"HP:0000453","label":"Choanal atresia"}]}},{"entity":"MGI:2665856","phenotype":{"types":[{"id":"MP:0008190","label":"decreased transitional stage B cell number"}]}},{"entity":"ClinVarVariant:7165","phenotype":{"types":[{"id":"HP:0000833","label":"Glucose intolerance"}]}},{"entity":"ClinVarVariant:4078","phenotype":{"types":[{"id":"HP:0000529","label":"Progressive visual loss"}]}},{"entity":"ClinVarVariant:204238","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:53925","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"MGI:1860953","phenotype":{"types":[{"id":"MP:0008470","label":"abnormal spleen B cell follicle morphology"}]}},{"entity":"ClinVarVariant:53256","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"MGI:2386947","phenotype":{"types":[{"id":"HP:0010831","label":"Impaired proprioception"}]}},{"entity":"ClinVarVariant:158721","phenotype":{"types":[{"id":"HP:0000499","label":"Abnormality of the eyelashes"}]}},{"entity":"ClinVarVariant:39468","phenotype":{"types":[{"id":"HP:0001845","label":"Overlapping toe"}]}},{"entity":"ClinVarVariant:53178","phenotype":{"types":[{"id":"HP:0004395","label":"Malnutrition"}]}},{"entity":"ClinVarVariant:158944","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00020820-WBRNAi00064595","phenotype":{"types":[{"id":"WBPhenotype:0000688","label":"sterile"}]}},{"entity":"ClinVarVariant:53499","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:53943","phenotype":{"types":[{"id":"HP:0001735","label":"Acute pancreatitis"}]}},{"entity":"ClinVarVariant:209145","phenotype":{"types":[{"id":"HP:0006101","label":"Finger syndactyly"}]}},{"entity":"WormBase:WBVar00275350","phenotype":{"types":[{"id":"WBPhenotype:0000135","label":"gene expression level high"}]}},{"entity":"ClinVarVariant:53620","phenotype":{"types":[{"id":"HP:0001548","label":"Overgrowth"}]}},{"entity":"ClinVarVariant:136034","phenotype":{"types":[{"id":"HP:0001587","label":"Primary ovarian failure"}]}},{"entity":"ClinVarVariant:10164","phenotype":{"types":[{"id":"HP:0001975","label":"Decreased platelet glycoprotein IIb-IIIa"}]}},{"entity":"ClinVarVariant:211738","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"ClinVarVariant:10083","phenotype":{"types":[{"id":"HP:0004374","label":"Hemiplegia/hemiparesis"}]}},{"entity":"ClinVarVariant:211636","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:8570","phenotype":{"types":[{"id":"HP:0011423","label":"Hyperchloremia"}]}},{"entity":"ClinVarVariant:46449","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:93762","phenotype":{"types":[{"id":"HP:0000668","label":"Hypodontia"}]}},{"entity":"FlyBase:FBal0210265","phenotype":{"types":[{"id":"FBbt:00005169PHENOTYPE","label":"Drosophila trichogen cell phenotype"}]}},{"entity":"ClinVarVariant:38990","phenotype":{"types":[{"id":"HP:0003458","label":"EMG: myopathic abnormalities"}]}},{"entity":"ClinVarVariant:216803","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:3602","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:5712","phenotype":{"types":[{"id":"HP:0001611","label":"Nasal speech"}]}},{"entity":"MGI:4459725","phenotype":{"types":[{"id":"MP:0002044","label":"increased colonic adenoma incidence"}]}},{"entity":"ClinVarVariant:41109","phenotype":{"types":[{"id":"HP:0010297","label":"Bifid tongue"}]}},{"entity":"ClinVarVariant:101374","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"MGI:1857312","phenotype":{"types":[{"id":"MP:0001666","label":"abnormal intestinal absorption"}]}},{"entity":"dbSNP:rs4149584","phenotype":{"types":[{"id":"HP:0002321","label":"Vertigo"}]}},{"entity":"ClinVarVariant:5746","phenotype":{"types":[{"id":"HP:0001622","label":"Premature birth"}]}},{"entity":"ClinVarVariant:53799","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"ClinVarVariant:50176","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:155800","phenotype":{"types":[{"id":"HP:0011034","label":"Amyloidosis"}]}},{"entity":"ClinVarVariant:36063","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:100773","phenotype":{"types":[{"id":"HP:0000104","label":"Renal agenesis"}]}},{"entity":"ClinVarVariant:6866","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"MGI:3527932","phenotype":{"types":[{"id":"MP:0002705","label":"dilated renal tubules"}]}},{"entity":"ClinVarVariant:9137","phenotype":{"types":[{"id":"HP:0003124","label":"Hypercholesterolemia"}]}},{"entity":"ClinVarVariant:181716","phenotype":{"types":[{"id":"HP:0100542","label":"Abnormal localization of kidney"}]}},{"entity":"ClinVarVariant:189941","phenotype":{"types":[{"id":"HP:0005484","label":"Postnatal microcephaly"}]}},{"entity":"ClinVarVariant:132825","phenotype":{"types":[{"id":"HP:0001660","label":"Truncus arteriosus"}]}},{"entity":"ClinVarVariant:133530","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:14519","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:13072","phenotype":{"types":[{"id":"HP:0009824","label":"Upper limb undergrowth"}]}},{"entity":"ClinVarVariant:156361","phenotype":{"types":[{"id":"HP:0000062","label":"Ambiguous genitalia"}]}},{"entity":"ClinVarVariant:13783","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:7623","phenotype":{"types":[{"id":"HP:0000772","label":"Abnormality of the ribs"}]}},{"entity":"MGI:3821974","phenotype":{"types":[{"id":"MP:0001463","label":"abnormal spatial learning"}]}},{"entity":"ClinVarVariant:120296","phenotype":{"types":[{"id":"HP:0001010","label":"Hypopigmentation of the skin"}]}},{"entity":"ClinVarVariant:127306","phenotype":{"types":[{"id":"HP:0008256","label":"Adrenocortical adenoma"}]}},{"entity":"ClinVarVariant:12873","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"ClinVarVariant:49281","phenotype":{"types":[{"id":"HP:0200024","label":"Premature chromatid separation"}]}},{"entity":"ClinVarVariant:211620","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"MGI:2384535","phenotype":{"types":[{"id":"MP:0001442","label":"decreased grooming behavior"}]}},{"entity":"ClinVarVariant:31180","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"ClinVarVariant:17088","phenotype":{"types":[{"id":"HP:0100279","label":"Ulcerative colitis"}]}},{"entity":"MGI:2653910","phenotype":{"types":[{"id":"MP:0008501","label":"increased IgG2b level"}]}},{"entity":"ClinVarVariant:1545","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"ClinVarVariant:53266","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:50949","phenotype":{"types":[{"id":"HP:0000817","label":"Poor eye contact"}]}},{"entity":"FlyBase:FBal0156488","phenotype":{"types":[{"id":"GO:0042600PHENOTYPE","label":"chorion phenotype"}]}},{"entity":"ClinVarVariant:41058","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:101132","phenotype":{"types":[{"id":"HP:0000490","label":"Deeply set eye"}]}},{"entity":"ClinVarVariant:127247","phenotype":{"types":[{"id":"HP:0001903","label":"Anemia"}]}},{"entity":"ClinVarVariant:53389","phenotype":{"types":[{"id":"HP:0000855","label":"Insulin resistance"}]}},{"entity":"ClinVarVariant:143808","phenotype":{"types":[{"id":"HP:0002376","label":"Developmental regression"}]}},{"entity":"ClinVarVariant:53545","phenotype":{"types":[{"id":"HP:0000670","label":"Carious teeth"}]}},{"entity":"ClinVarVariant:65904","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"_:genid1972746","phenotype":{"types":[{"id":"ZP:0001671","label":"abnormal(ly) disrupted locomotory behavior"}]}},{"entity":"ClinVarVariant:6040","phenotype":{"types":[{"id":"HP:0000218","label":"High palate"}]}},{"entity":"MGI:5527336","phenotype":{"types":[{"id":"MP:0010639","label":"altered tumor pathology"}]}},{"entity":"ClinVarVariant:102556","phenotype":{"types":[{"id":"HP:0000709","label":"Psychosis"}]}},{"entity":"FlyBase:FBal0205295","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"ClinVarVariant:21350","phenotype":{"types":[{"id":"HP:0000975","label":"Hyperhidrosis"}]}},{"entity":"ClinVarVariant:54074","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"MGI:1861186","phenotype":{"types":[{"id":"MP:0004473","label":"absent nasal bone"}]}},{"entity":"ClinVarVariant:52388","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"ClinVarVariant:42069","phenotype":{"types":[{"id":"HP:0002720","label":"IgA deficiency"}]}},{"entity":"ClinVarVariant:68059","phenotype":{"types":[{"id":"HP:0011704","label":"Sick sinus syndrome"}]}},{"entity":"MGI:2153356","phenotype":{"types":[{"id":"HP:0003687","label":"Centrally nucleated skeletal muscle fibers"}]}},{"entity":"ClinVarVariant:15624","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"ClinVarVariant:197669","phenotype":{"types":[{"id":"HP:0010783","label":"Erythema"}]}},{"entity":"ClinVarVariant:7256","phenotype":{"types":[{"id":"HP:0002619","label":"Varicose veins"}]}},{"entity":"ClinVarVariant:36838","phenotype":{"types":[{"id":"HP:0001738","label":"Exocrine pancreatic insufficiency"}]}},{"entity":"ClinVarVariant:21094","phenotype":{"types":[{"id":"HP:0000995","label":"Melanocytic nevus"}]}},{"entity":"ClinVarVariant:53431","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"AQTL:24319","phenotype":{"types":[{"id":"AQTLTrait:1090","label":"Longissimus muscle area"}]}},{"entity":"ClinVarVariant:215458","phenotype":{"types":[{"id":"HP:0000501","label":"Glaucoma"}]}},{"entity":"ClinVarVariant:158744","phenotype":{"types":[{"id":"HP:0000851","label":"Congenital hypothyroidism"}]}},{"entity":"ClinVarVariant:39713","phenotype":{"types":[{"id":"HP:0000194","label":"Open mouth"}]}},{"entity":"ClinVarVariant:36073","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:165770","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:4321","phenotype":{"types":[{"id":"HP:0000740","label":"Anxiety (with pheochromocytoma)"}]}},{"entity":"ClinVarVariant:4179","phenotype":{"types":[{"id":"HP:0001332","label":"Dystonia"}]}},{"entity":"MGI:4435548","phenotype":{"types":[{"id":"MP:0002418","label":"increased susceptibility to viral infection"}]}},{"entity":"ClinVarVariant:50071","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:40493","phenotype":{"types":[{"id":"HP:0000824","label":"Growth hormone deficiency"}]}},{"entity":"ClinVarVariant:9192","phenotype":{"types":[{"id":"HP:0012307","label":"Spatulate ribs"}]}},{"entity":"ClinVarVariant:49601","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:31911","phenotype":{"types":[{"id":"HP:0000384","label":"Preauricular skin tag"}]}},{"entity":"ClinVarVariant:9767","phenotype":{"types":[{"id":"HP:0003236","label":"Elevated serum creatine phosphokinase"}]}},{"entity":"ClinVarVariant:66505","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:1578","phenotype":{"types":[{"id":"HP:0002487","label":"Hyperkinesis"}]}},{"entity":"ClinVarVariant:10048","phenotype":{"types":[{"id":"HP:0003149","label":"Hyperuricosuria"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004397-WBRNAi00089816","phenotype":{"types":[{"id":"WBPhenotype:0000583","label":"dumpy"}]}},{"entity":"ClinVarVariant:10166","phenotype":{"types":[{"id":"HP:0005268","label":"Spontaneous abortion"}]}},{"entity":"ClinVarVariant:8653","phenotype":{"types":[{"id":"HP:0000348","label":"High forehead"}]}},{"entity":"ClinVarVariant:17939","phenotype":{"types":[{"id":"HP:0010517","label":"Ectopic thymus tissue"}]}},{"entity":"MGI:1856276","phenotype":{"types":[{"id":"MP:0000914","label":"exencephaly"}]}},{"entity":"ClinVarVariant:1740","phenotype":{"types":[{"id":"HP:0001511","label":"Intrauterine growth retardation"}]}},{"entity":"ClinVarVariant:93124","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:53310","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"ClinVarVariant:91640","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"NCBIGene:100126595","phenotype":{"types":[{"id":"HP:0100771","label":"Hypoperistalsis"}]}},{"entity":"ClinVarVariant:11715","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"MGI:2447334","phenotype":{"types":[{"id":"HP:0012757","label":"Abnormal neuron morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00008149-WBRNAi00008529","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:49227","phenotype":{"types":[{"id":"HP:0009729","label":"Cardiac rhabdomyoma"}]}},{"entity":"ClinVarVariant:143544","phenotype":{"types":[{"id":"HP:0001063","label":"Acrocyanosis"}]}},{"entity":"dbSNP:rs81339346","phenotype":{"types":[{"id":"AQTLTrait:1483","label":"Red blood cell count"}]}},{"entity":"ClinVarVariant:127155","phenotype":{"types":[{"id":"HP:0000622","label":"Blurred vision"}]}},{"entity":"ClinVarVariant:102444","phenotype":{"types":[{"id":"HP:0000561","label":"Absent eyelashes"}]}},{"entity":"MGI:1857139","phenotype":{"types":[{"id":"MP:0000528","label":"delayed kidney development"}]}},{"entity":"ClinVarVariant:158964","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:49611","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:17384","phenotype":{"types":[{"id":"HP:0000347","label":"Micrognathia"}]}},{"entity":"ClinVarVariant:216211","phenotype":{"types":[{"id":"HP:0001272","label":"Cerebellar atrophy"}]}},{"entity":"MGI:3758075","phenotype":{"types":[{"id":"MP:0000822","label":"abnormal brain ventricle morphology"}]}},{"entity":"ClinVarVariant:29712","phenotype":{"types":[{"id":"HP:0002841","label":"Recurrent fungal infections"}]}},{"entity":"MGI:1857314","phenotype":{"types":[{"id":"MP:0011093","label":"embryonic lethality at implantation, complete penetrance"}]}},{"entity":"ClinVarVariant:217430","phenotype":{"types":[{"id":"HP:0001820","label":"Leukonychia"}]}},{"entity":"MGI:4421830","phenotype":{"types":[{"id":"HP:0012864","label":"Abnormal sperm morphology"}]}},{"entity":"ClinVarVariant:198077","phenotype":{"types":[{"id":"HP:0001638","label":"Cardiomyopathy"}]}},{"entity":"MGI:1857229","phenotype":{"types":[{"id":"MP:0000260","label":"abnormal angiogenesis"}]}},{"entity":"MGI:3806024","phenotype":{"types":[{"id":"HP:0011273","label":"Anisocytosis"}]}},{"entity":"ClinVarVariant:50907","phenotype":{"types":[{"id":"HP:0001043","label":"Prominent scalp veins"}]}},{"entity":"ClinVarVariant:3851","phenotype":{"types":[{"id":"HP:0000787","label":"Nephrolithiasis"}]}},{"entity":"ClinVarVariant:40599","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:9597","phenotype":{"types":[{"id":"HP:0001700","label":"Myocardial necrosis"}]}},{"entity":"ClinVarVariant:39524","phenotype":{"types":[{"id":"HP:0000164","label":"Abnormality of the teeth"}]}},{"entity":"ClinVarVariant:16287","phenotype":{"types":[{"id":"HP:0001363","label":"Craniosynostosis"}]}},{"entity":"MGI:3663386","phenotype":{"types":[{"id":"MP:0005449","label":"abnormal food intake"}]}},{"entity":"ClinVarVariant:12345","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:11012","phenotype":{"types":[{"id":"HP:0001298","label":"Encephalopathy"}]}},{"entity":"ClinVarVariant:53276","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:53901","phenotype":{"types":[{"id":"HP:0003453","label":"Antineutrophil antibody positivity"}]}},{"entity":"MGI:3811603","phenotype":{"types":[{"id":"HP:0003097","label":"Short femur"}]}},{"entity":"ClinVarVariant:6925","phenotype":{"types":[{"id":"HP:0000822","label":"Hypertension"}]}},{"entity":"ClinVarVariant:11788","phenotype":{"types":[{"id":"HP:0007354","label":"Amyotrophic lateral sclerosis"}]}},{"entity":"ClinVarVariant:54083","phenotype":{"types":[{"id":"HP:0006536","label":"Obstructive lung disease"}]}},{"entity":"ClinVarVariant:11722","phenotype":{"types":[{"id":"HP:0001537","label":"Umbilical hernia"}]}},{"entity":"ClinVarVariant:210318","phenotype":{"types":[{"id":"HP:0002024","label":"Malabsorption"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006996-WBRNAi00007928","phenotype":{"types":[{"id":"WBPhenotype:0001168","label":"pseudocleavage absent early emb"}]}},{"entity":"ClinVarVariant:182830","phenotype":{"types":[{"id":"HP:0100587","label":"Abnormality of the preputium"}]}},{"entity":"ClinVarVariant:6165","phenotype":{"types":[{"id":"HP:0006789","label":"Mitochondrial encephalopathy"}]}},{"entity":"dbSNP:rs7903146","phenotype":{"types":[{"id":"HP:0100710","label":"Impulsivity"}]}},{"entity":"ClinVarVariant:24926","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:65048","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:6822","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"MGI:3046573","phenotype":{"types":[{"id":"MP:0011085","label":"postnatal lethality, complete penetrance"}]}},{"entity":"ClinVarVariant:21278","phenotype":{"types":[{"id":"HP:0001222","label":"Spatulate thumbs"}]}},{"entity":"ClinVarVariant:56227","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:155948","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"dbSNP:rs1027643","phenotype":{"types":[{"id":"HP:0000526","label":"Aniridia"}]}},{"entity":"_:genid1976410","phenotype":{"types":[{"id":"ZP:0000868","label":"abnormal(ly) disrupted convergent extension involved in gastrulation"}]}},{"entity":"ClinVarVariant:8267","phenotype":{"types":[{"id":"HP:0002586","label":"Peritonitis"}]}},{"entity":"ClinVarVariant:189559","phenotype":{"types":[{"id":"HP:0011097","label":"Epileptic spasms"}]}},{"entity":"ClinVarVariant:2676","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:3621117","phenotype":{"types":[{"id":"HP:0000938","label":"Osteopenia"}]}},{"entity":"ClinVarVariant:159096","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"http://www.monarchinitiative.org/_ZDB-GENE-050306-15-ZDB-MRPHLNO-100618-3","phenotype":{"types":[{"id":"GO:0060538PHENOTYPE","label":"skeletal muscle organ development phenotype"}]}},{"entity":"ClinVarVariant:211646","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:189579","phenotype":{"types":[{"id":"HP:0001336","label":"Myoclonus"}]}},{"entity":"ClinVarVariant:126807","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"ClinVarVariant:14052","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"MGI:5563785","phenotype":{"types":[{"id":"MP:0009347","label":"increased trabecular bone thickness"}]}},{"entity":"ClinVarVariant:36083","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:195458","phenotype":{"types":[{"id":"HP:0007370","label":"Aplasia/Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:4300","phenotype":{"types":[{"id":"HP:0003540","label":"Impaired platelet aggregation"}]}},{"entity":"ClinVarVariant:194115","phenotype":{"types":[{"id":"HP:0000962","label":"Hyperkeratosis"}]}},{"entity":"ClinVarVariant:67967","phenotype":{"types":[{"id":"HP:0003115","label":"Abnormal EKG"}]}},{"entity":"ClinVarVariant:16839","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"MGI:4459093","phenotype":{"types":[{"id":"HP:0010831","label":"Impaired proprioception"}]}},{"entity":"ClinVarVariant:209134","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:178847","phenotype":{"types":[{"id":"HP:0001742","label":"Nasal obstruction"}]}},{"entity":"ClinVarVariant:68699","phenotype":{"types":[{"id":"HP:0100530","label":"Abnormality of calcium-phosphate metabolism"}]}},{"entity":"MGI:1856217","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"ClinVarVariant:189359","phenotype":{"types":[{"id":"HP:0000709","label":"Psychosis"}]}},{"entity":"MGI:3510782","phenotype":{"types":[{"id":"MP:0008699","label":"increased interleukin-4 secretion"}]}},{"entity":"MGI:2447199","phenotype":{"types":[{"id":"MP:0000932","label":"absent notochord"}]}},{"entity":"FlyBase:FBal0207596","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:42079","phenotype":{"types":[{"id":"HP:0002720","label":"IgA deficiency"}]}},{"entity":"ClinVarVariant:143802","phenotype":{"types":[{"id":"HP:0002020","label":"Gastroesophageal reflux"}]}},{"entity":"ClinVarVariant:7622","phenotype":{"types":[{"id":"HP:0000545","label":"Myopia"}]}},{"entity":"MGI:5295747","phenotype":{"types":[{"id":"HP:0003292","label":"Decreased serum leptin"}]}},{"entity":"ClinVarVariant:884","phenotype":{"types":[{"id":"HP:0002318","label":"Cervical myelopathy"}]}},{"entity":"ClinVarVariant:204096","phenotype":{"types":[{"id":"HP:0000965","label":"Cutis marmorata"}]}},{"entity":"ClinVarVariant:1389","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"ClinVarVariant:94230","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"ClinVarVariant:49530","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"ClinVarVariant:30696","phenotype":{"types":[{"id":"HP:0000256","label":"Macrocephaly"}]}},{"entity":"WormBase:WBVar00146313","phenotype":{"types":[{"id":"WBPhenotype:0000962","label":"level of transgene expression variant"}]}},{"entity":"ClinVarVariant:53294","phenotype":{"types":[{"id":"HP:0000737","label":"Irritability"}]}},{"entity":"ClinVarVariant:53935","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"MGI:3757964","phenotype":{"types":[{"id":"HP:0001719","label":"Double outlet right ventricle"}]}},{"entity":"ClinVarVariant:53738","phenotype":{"types":[{"id":"HP:0000718","label":"Aggressive behavior"}]}},{"entity":"ClinVarVariant:193517","phenotype":{"types":[{"id":"HP:0000992","label":"Cutaneous photosensitivity"}]}},{"entity":"MGI:1857930","phenotype":{"types":[{"id":"HP:0011804","label":"Abnormality of muscle physiology"}]}},{"entity":"ClinVarVariant:68711","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:158339","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:6718","phenotype":{"types":[{"id":"HP:0001908","label":"Hypoplastic anemia"}]}},{"entity":"ClinVarVariant:94139","phenotype":{"types":[{"id":"HP:0002353","label":"EEG abnormality"}]}},{"entity":"ClinVarVariant:45115","phenotype":{"types":[{"id":"HP:0002859","label":"Rhabdomyosarcoma"}]}},{"entity":"MGI:2678305","phenotype":{"types":[{"id":"MP:0002169","label":"no abnormal phenotype detected"}]}},{"entity":"ClinVarVariant:158974","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:9236","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000067-WBRNAi00085673","phenotype":{"types":[{"id":"WBPhenotype:0001260","label":"oocyte morphology variant"}]}},{"entity":"ClinVarVariant:4262","phenotype":{"types":[{"id":"HP:0005177","label":"Premature arteriosclerosis"}]}},{"entity":"ClinVarVariant:42327","phenotype":{"types":[{"id":"HP:0003088","label":"Premature osteoarthritis"}]}},{"entity":"dbSNP:rs6729815","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"MGI:3840238","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:65058","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:36091","phenotype":{"types":[{"id":"HP:0001763","label":"Pes planus"}]}},{"entity":"ClinVarVariant:7360","phenotype":{"types":[{"id":"HP:0005978","label":"Type II diabetes mellitus"}]}},{"entity":"ClinVarVariant:5225","phenotype":{"types":[{"id":"HP:0011003","label":"Severe Myopia"}]}},{"entity":"ClinVarVariant:65166","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"MGI:3832033","phenotype":{"types":[{"id":"HP:0000078","label":"Abnormality of the genital system"}]}},{"entity":"ClinVarVariant:10761","phenotype":{"types":[{"id":"HP:0001658","label":"Myocardial infarction"}]}},{"entity":"ClinVarVariant:210456","phenotype":{"types":[{"id":"HP:0001382","label":"Joint hypermobility"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00003401-WBRNAi00085349","phenotype":{"types":[{"id":"WBPhenotype:0001944","label":"oocyte number decreased"}]}},{"entity":"ClinVarVariant:42089","phenotype":{"types":[{"id":"HP:0002720","label":"IgA deficiency"}]}},{"entity":"FlyBase:FBal0119169","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:186362","phenotype":{"types":[{"id":"HP:0001908","label":"Hypoplastic anemia"}]}},{"entity":"ClinVarVariant:127417","phenotype":{"types":[{"id":"HP:0000524","label":"Conjunctival telangiectasia"}]}},{"entity":"ClinVarVariant:39785","phenotype":{"types":[{"id":"HP:0000772","label":"Abnormality of the ribs"}]}},{"entity":"MGI:1857212","phenotype":{"types":[{"id":"MP:0005458","label":"increased percent body fat/body weight"}]}},{"entity":"ClinVarVariant:143525","phenotype":{"types":[{"id":"HP:0000729","label":"Autistic behavior"}]}},{"entity":"ClinVarVariant:101294","phenotype":{"types":[{"id":"HP:0100689","label":"Decreased corneal thickness"}]}},{"entity":"ClinVarVariant:167361","phenotype":{"types":[{"id":"HP:0000369","label":"Low-set ears"}]}},{"entity":"ClinVarVariant:16342","phenotype":{"types":[{"id":"HP:0003811","label":"Neonatal death"}]}},{"entity":"MGI:1857722","phenotype":{"types":[{"id":"MP:0012165","label":"absent neural folds"}]}},{"entity":"ClinVarVariant:159921","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:12023","phenotype":{"types":[{"id":"HP:0010978","label":"Abnormality of immune system physiology"}]}},{"entity":"ZFIN:ZDB-ALT-040929-4","phenotype":{"types":[{"id":"ZP:0000043","label":"abnormal(ly) decreased size eye"}]}},{"entity":"ClinVarVariant:10118","phenotype":{"types":[{"id":"HP:0005542","label":"Prolonged whole-blood clotting time"}]}},{"entity":"MGI:2176049","phenotype":{"types":[{"id":"HP:0002414","label":"Spina bifida"}]}},{"entity":"ClinVarVariant:53923","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"ClinVarVariant:49631","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:36093","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:35890","phenotype":{"types":[{"id":"HP:0003040","label":"Arthropathy"}]}},{"entity":"dbSNP:rs109529219","phenotype":{"types":[{"id":"AQTLTrait:1040","label":"Milk protein percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:8875","phenotype":{"types":[{"id":"HP:0009773","label":"Symphalangism affecting the phalanges of the hand"}]}},{"entity":"MGI:5548830","phenotype":{"types":[{"id":"MP:0010123","label":"increased bone mineral content"}]}},{"entity":"ClinVarVariant:141944","phenotype":{"types":[{"id":"HP:0005374","label":"Cellular immunodeficiency"}]}},{"entity":"ClinVarVariant:40068","phenotype":{"types":[{"id":"HP:0000105","label":"Enlarged kidneys"}]}},{"entity":"ClinVarVariant:7427","phenotype":{"types":[{"id":"HP:0100015","label":"Stahl ear"}]}},{"entity":"MGI:1931521","phenotype":{"types":[{"id":"MP:0005296","label":"abnormal humerus morphology"}]}},{"entity":"ClinVarVariant:10288","phenotype":{"types":[{"id":"HP:0012062","label":"Bone cyst"}]}},{"entity":"FlyBase:FBal0178561","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"MGI:3623277","phenotype":{"types":[{"id":"MP:0003944","label":"abnormal T cell subpopulation ratio"}]}},{"entity":"ClinVarVariant:217280","phenotype":{"types":[{"id":"HP:0006808","label":"Cerebral hypomyelination"}]}},{"entity":"FlyBase:FBal0205457","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"FlyBase:FBal0208360","phenotype":{"types":[{"id":"FBcv:0000351","label":"lethal"}]}},{"entity":"ClinVarVariant:143818","phenotype":{"types":[{"id":"HP:0002376","label":"Developmental regression"}]}},{"entity":"ClinVarVariant:39715","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:210399","phenotype":{"types":[{"id":"HP:0011362","label":"Abnormal hair quantity"}]}},{"entity":"ClinVarVariant:94837","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"MGI:5468252","phenotype":{"types":[{"id":"MP:0011167","label":"abnormal adipose tissue development"}]}},{"entity":"FlyBase:FBal0203318","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:42391","phenotype":{"types":[{"id":"HP:0010550","label":"Paraplegia"}]}},{"entity":"ClinVarVariant:333","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"MGI:4360523","phenotype":{"types":[{"id":"MP:0003697","label":"absent zona pellucida"}]}},{"entity":"ClinVarVariant:127329","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:12586","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:217078","phenotype":{"types":[{"id":"HP:0007440","label":"Generalized hyperpigmentation"}]}},{"entity":"ClinVarVariant:54084","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:211656","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"MGI:4939621","phenotype":{"types":[{"id":"MP:0005670","label":"abnormal white adipose tissue physiology"}]}},{"entity":"FlyBase:FBal0260939","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:2267","phenotype":{"types":[{"id":"HP:0100279","label":"Ulcerative colitis"}]}},{"entity":"ClinVarVariant:137984","phenotype":{"types":[{"id":"HP:0000707","label":"Abnormality of the nervous system"}]}},{"entity":"MGI:3810074","phenotype":{"types":[{"id":"MP:0005092","label":"decreased double-positive T cell number"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002299-WBRNAi00078911","phenotype":{"types":[{"id":"WBPhenotype:0000666","label":"ovulation variant"}]}},{"entity":"ClinVarVariant:210464","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:215893","phenotype":{"types":[{"id":"HP:0000107","label":"Renal cyst"}]}},{"entity":"ClinVarVariant:41085","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"ClinVarVariant:133628","phenotype":{"types":[{"id":"HP:0002344","label":"Progressive neurologic deterioration"}]}},{"entity":"ClinVarVariant:180354","phenotype":{"types":[{"id":"HP:0002631","label":"Ascending aortic aneurysm"}]}},{"entity":"ClinVarVariant:135745","phenotype":{"types":[{"id":"HP:0001009","label":"Telangiectasia"}]}},{"entity":"ClinVarVariant:208846","phenotype":{"types":[{"id":"HP:0001716","label":"Wolff-Parkinson-White syndrome"}]}},{"entity":"MGI:2158692","phenotype":{"types":[{"id":"MP:0002566","label":"abnormal sexual interaction"}]}},{"entity":"MGI:2183240","phenotype":{"types":[{"id":"MP:0006143","label":"increased systemic arterial diastolic blood pressure"}]}},{"entity":"ClinVarVariant:41001","phenotype":{"types":[{"id":"HP:0001376","label":"Limitation of joint mobility"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00021604-WBRNAi00007532","phenotype":{"types":[{"id":"WBPhenotype:0001119","label":"cell cycle slow early emb"}]}},{"entity":"ClinVarVariant:128203","phenotype":{"types":[{"id":"HP:0000520","label":"Proptosis"}]}},{"entity":"ClinVarVariant:9966","phenotype":{"types":[{"id":"HP:0001923","label":"Reticulocytosis"}]}},{"entity":"ClinVarVariant:31190","phenotype":{"types":[{"id":"HP:0002269","label":"Abnormality of neuronal migration"}]}},{"entity":"ClinVarVariant:216404","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:120223","phenotype":{"types":[{"id":"HP:0000953","label":"Hyperpigmentation of the skin"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00000912-WBRNAi00066508","phenotype":{"types":[{"id":"WBPhenotype:0000061","label":"extended life span"}]}},{"entity":"ClinVarVariant:10259","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:3773724","phenotype":{"types":[{"id":"MP:0001265","label":"decreased body size"}]}},{"entity":"ClinVarVariant:216414","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:53459","phenotype":{"types":[{"id":"HP:0100806","label":"Sepsis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017967-WBRNAi00000357","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:343","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"MGI:2153811","phenotype":{"types":[{"id":"MP:0000035","label":"abnormal membranous labyrinth morphology"}]}},{"entity":"ClinVarVariant:97534","phenotype":{"types":[{"id":"HP:0000999","label":"Pyoderma"}]}},{"entity":"ClinVarVariant:30262","phenotype":{"types":[{"id":"HP:0000546","label":"Retinal degeneration"}]}},{"entity":"ClinVarVariant:56237","phenotype":{"types":[{"id":"HP:0002072","label":"Chorea"}]}},{"entity":"ClinVarVariant:4784","phenotype":{"types":[{"id":"HP:0000486","label":"Strabismus"}]}},{"entity":"ClinVarVariant:188125","phenotype":{"types":[{"id":"HP:0012539","label":"Non-Hodgkin lymphoma"}]}},{"entity":"ClinVarVariant:50237","phenotype":{"types":[{"id":"HP:0003300","label":"Ovoid vertebral bodies"}]}},{"entity":"ClinVarVariant:100931","phenotype":{"types":[{"id":"HP:0004375","label":"Neoplasm of the nervous system"}]}},{"entity":"ClinVarVariant:9993","phenotype":{"types":[{"id":"HP:0001761","label":"Pes cavus"}]}},{"entity":"ClinVarVariant:132699","phenotype":{"types":[{"id":"HP:0001161","label":"Hand polydactyly"}]}},{"entity":"FlyBase:FBal0277862","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ZFIN:ZDB-ALT-121128-4","phenotype":{"types":[{"id":"ZP:0002448","label":"abnormal(ly) disorganized retinal outer nuclear layer"}]}},{"entity":"ClinVarVariant:158984","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:5855","phenotype":{"types":[{"id":"HP:0000217","label":"Xerostomia"}]}},{"entity":"ClinVarVariant:14030","phenotype":{"types":[{"id":"HP:0001601","label":"Laryngomalacia"}]}},{"entity":"ClinVarVariant:210007","phenotype":{"types":[{"id":"HP:0002119","label":"Ventriculomegaly"}]}},{"entity":"FlyBase:FBal0098633","phenotype":{"types":[{"id":"FBcv:0000364","label":"sterile"}]}},{"entity":"ClinVarVariant:216764","phenotype":{"types":[{"id":"HP:0000256","label":"Macrocephaly"}]}},{"entity":"ClinVarVariant:143828","phenotype":{"types":[{"id":"HP:0002376","label":"Developmental regression"}]}},{"entity":"ClinVarVariant:96607","phenotype":{"types":[{"id":"HP:0010906","label":"Hyperhistidinemia"}]}},{"entity":"MGI:2651830","phenotype":{"types":[{"id":"MP:0001053","label":"abnormal neuromuscular synapse morphology"}]}},{"entity":"ClinVarVariant:88650","phenotype":{"types":[{"id":"HP:0002408","label":"Cerebral arteriovenous malformation"}]}},{"entity":"FlyBase:FBal0304837","phenotype":{"types":[{"id":"FBbt:00001778PHENOTYPE","label":"Drosophila wing disc phenotype"}]}},{"entity":"ClinVarVariant:162493","phenotype":{"types":[{"id":"HP:0001639","label":"Hypertrophic cardiomyopathy"}]}},{"entity":"ClinVarVariant:35601","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:1282","phenotype":{"types":[{"id":"HP:0003398","label":"Abnormal synaptic transmission at the neuromuscular junction"}]}},{"entity":"ClinVarVariant:36041","phenotype":{"types":[{"id":"HP:0002104","label":"Apnea"}]}},{"entity":"ClinVarVariant:21545","phenotype":{"types":[{"id":"HP:0001256","label":"Intellectual disability, mild"}]}},{"entity":"ClinVarVariant:65068","phenotype":{"types":[{"id":"HP:0002514","label":"Cerebral calcification"}]}},{"entity":"ClinVarVariant:13909","phenotype":{"types":[{"id":"HP:0002527","label":"Falls"}]}},{"entity":"ClinVarVariant:162416","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"dbSNP:rs110710505","phenotype":{"types":[{"id":"AQTLTrait:1120","label":"Thurl width"}]}},{"entity":"ClinVarVariant:5867","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:216132","phenotype":{"types":[{"id":"HP:0000505","label":"Visual impairment"}]}},{"entity":"ClinVarVariant:142766","phenotype":{"types":[{"id":"HP:0001067","label":"Neurofibromas"}]}},{"entity":"ClinVarVariant:592","phenotype":{"types":[{"id":"HP:0002286","label":"Fair hair"}]}},{"entity":"ClinVarVariant:94437","phenotype":{"types":[{"id":"HP:0001371","label":"Flexion contracture"}]}},{"entity":"ClinVarVariant:13326","phenotype":{"types":[{"id":"HP:0000978","label":"Bruising susceptibility"}]}},{"entity":"ClinVarVariant:7726","phenotype":{"types":[{"id":"HP:0000114","label":"Proximal tubulopathy"}]}},{"entity":"MGI:3624262","phenotype":{"types":[{"id":"HP:0000089","label":"Renal hypoplasia"}]}},{"entity":"ClinVarVariant:49932","phenotype":{"types":[{"id":"HP:0006772","label":"Renal angiomyolipoma"}]}},{"entity":"MGI:4262238","phenotype":{"types":[{"id":"GO:0003351PHENOTYPE","label":"epithelial cilium movement phenotype"}]}},{"entity":"ClinVarVariant:65879","phenotype":{"types":[{"id":"HP:0000054","label":"Micropenis"}]}},{"entity":"FlyBase:FBal0297156","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:101115","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"ClinVarVariant:53185","phenotype":{"types":[{"id":"HP:0000031","label":"Epididymitis"}]}},{"entity":"ClinVarVariant:209063","phenotype":{"types":[{"id":"HP:0001648","label":"Cor pulmonale"}]}},{"entity":"ClinVarVariant:56283","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:10629","phenotype":{"types":[{"id":"HP:0001892","label":"Abnormal bleeding"}]}},{"entity":"ClinVarVariant:127244","phenotype":{"types":[{"id":"HP:0008734","label":"Decreased testicular size"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00001102-WBRNAi00067595","phenotype":{"types":[{"id":"WBPhenotype:0000531","label":"organism development variant"}]}},{"entity":"ClinVarVariant:67858","phenotype":{"types":[{"id":"HP:0004756","label":"Ventricular tachycardia"}]}},{"entity":"ClinVarVariant:135922","phenotype":{"types":[{"id":"HP:0002672","label":"Gastrointestinal carcinoma"}]}},{"entity":"ClinVarVariant:35825","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:39594","phenotype":{"types":[{"id":"HP:0002079","label":"Hypoplasia of the corpus callosum"}]}},{"entity":"ClinVarVariant:143592","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"MGI:2152978","phenotype":{"types":[{"id":"MP:0004669","label":"enlarged vertebral body"}]}},{"entity":"FlyBase:FBal0210008","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:179260","phenotype":{"types":[{"id":"HP:0000358","label":"Posteriorly rotated ears"}]}},{"entity":"ClinVarVariant:53376","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:40680","phenotype":{"types":[{"id":"HP:0003010","label":"Prolonged bleeding time"}]}},{"entity":"ClinVarVariant:21242","phenotype":{"types":[{"id":"HP:0000202","label":"Oral cleft"}]}},{"entity":"ClinVarVariant:211666","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:3441","phenotype":{"types":[{"id":"HP:0001199","label":"Triphalangeal thumb"}]}},{"entity":"ClinVarVariant:17082","phenotype":{"types":[{"id":"HP:0100608","label":"Metrorrhagia"}]}},{"entity":"ClinVarVariant:159244","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"MGI:2148205","phenotype":{"types":[{"id":"MP:0004236","label":"absent masseter muscle"}]}},{"entity":"ClinVarVariant:9246","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:188766","phenotype":{"types":[{"id":"HP:0000635","label":"Blue irides"}]}},{"entity":"ClinVarVariant:24502","phenotype":{"types":[{"id":"HP:0000099","label":"Glomerulonephritis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00012632-WBRNAi00067998","phenotype":{"types":[{"id":"WBPhenotype:0000531","label":"organism development variant"}]}},{"entity":"ClinVarVariant:24601","phenotype":{"types":[{"id":"HP:0000003","label":"Multicystic kidney dysplasia"}]}},{"entity":"ClinVarVariant:188938","phenotype":{"types":[{"id":"HP:0000789","label":"Infertility"}]}},{"entity":"ClinVarVariant:10263","phenotype":{"types":[{"id":"HP:0005681","label":"Juvenile rheumatoid arthritis"}]}},{"entity":"ClinVarVariant:49641","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"MGI:3771975","phenotype":{"types":[{"id":"MP:0000458","label":"abnormal mandible morphology"}]}},{"entity":"MGI:3765956","phenotype":{"types":[{"id":"GO:0042981PHENOTYPE","label":"regulation of apoptotic process phenotype"}]}},{"entity":"ClinVarVariant:18452","phenotype":{"types":[{"id":"HP:0000047","label":"Hypospadias"}]}},{"entity":"ClinVarVariant:29740","phenotype":{"types":[{"id":"HP:0010628","label":"Facial palsy"}]}},{"entity":"ClinVarVariant:216584","phenotype":{"types":[{"id":"HP:0006771","label":"Duodenal adenocarcinoma"}]}},{"entity":"ClinVarVariant:204313","phenotype":{"types":[{"id":"HP:0001989","label":"Fetal akinesia sequence"}]}},{"entity":"ClinVarVariant:4442","phenotype":{"types":[{"id":"HP:0001947","label":"Renal tubular acidosis"}]}},{"entity":"ClinVarVariant:120219","phenotype":{"types":[{"id":"HP:0001055","label":"Erysipelas"}]}},{"entity":"ClinVarVariant:158070","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"ClinVarVariant:93153","phenotype":{"types":[{"id":"HP:0002202","label":"Pleural effusion"}]}},{"entity":"ClinVarVariant:12391","phenotype":{"types":[{"id":"HP:0000708","label":"Behavioral abnormality"}]}},{"entity":"ClinVarVariant:97700","phenotype":{"types":[{"id":"HP:0001596","label":"Alopecia"}]}},{"entity":"ClinVarVariant:10832","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"MGI:3778272","phenotype":{"types":[{"id":"HP:0003202","label":"Skeletal muscle atrophy"}]}},{"entity":"ClinVarVariant:16646","phenotype":{"types":[{"id":"HP:0007110","label":"Central hypoventilation"}]}},{"entity":"ClinVarVariant:49661","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:24686","phenotype":{"types":[{"id":"HP:0001902","label":"Giant platelets"}]}},{"entity":"ClinVarVariant:158186","phenotype":{"types":[{"id":"HP:0011097","label":"Epileptic spasms"}]}},{"entity":"FlyBase:FBal0300880","phenotype":{"types":[{"id":"GO:0005634PHENOTYPE","label":"nucleus phenotype"}]}},{"entity":"ClinVarVariant:25360","phenotype":{"types":[{"id":"HP:0001987","label":"Hyperammonemia"}]}},{"entity":"WormBase:WBVar00144564","phenotype":{"types":[{"id":"WBPhenotype:0000687","label":"feminization of XX and XO animals"}]}},{"entity":"FlyBase:FBal0213074","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:52378","phenotype":{"types":[{"id":"HP:0003002","label":"Breast carcinoma"}]}},{"entity":"MGI:5518726","phenotype":{"types":[{"id":"MP:0000715","label":"decreased thymocyte number"}]}},{"entity":"ClinVarVariant:135736","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"_:genid1974728","phenotype":{"types":[{"id":"ZP:0001828","label":"abnormal(ly) malformed post-vent region"}]}},{"entity":"ClinVarVariant:5095","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"MGI:2183400","phenotype":{"types":[{"id":"MP:0005026","label":"decreased susceptibility to parasitic infection"}]}},{"entity":"ClinVarVariant:16275","phenotype":{"types":[{"id":"HP:0001909","label":"Leukemia"}]}},{"entity":"MGI:2180768","phenotype":{"types":[{"id":"HP:0000777","label":"Abnormality of the thymus"}]}},{"entity":"MGI:5449635","phenotype":{"types":[{"id":"MP:0001661","label":"extended life span"}]}},{"entity":"FlyBase:FBal0268099","phenotype":{"types":[{"id":"FBbt:00004508PHENOTYPE","label":"eye phenotype"}]}},{"entity":"ClinVarVariant:3766","phenotype":{"types":[{"id":"HP:0001789","label":"Hydrops fetalis"}]}},{"entity":"ClinVarVariant:55941","phenotype":{"types":[{"id":"HP:0005280","label":"Depressed nasal bridge"}]}},{"entity":"ClinVarVariant:53915","phenotype":{"types":[{"id":"HP:0010943","label":"Echogenic fetal bowel"}]}},{"entity":"ClinVarVariant:126447","phenotype":{"types":[{"id":"HP:0000613","label":"Photophobia"}]}},{"entity":"ClinVarVariant:353","phenotype":{"types":[{"id":"HP:0002521","label":"Hypsarrhythmia"}]}},{"entity":"ClinVarVariant:211728","phenotype":{"types":[{"id":"HP:0003272","label":"Abnormality of the hip bone"}]}},{"entity":"ClinVarVariant:24518","phenotype":{"types":[{"id":"HP:0001730","label":"Progressive hearing impairment"}]}},{"entity":"ClinVarVariant:216185","phenotype":{"types":[{"id":"HP:0006744","label":"Adrenocortical carcinoma"}]}},{"entity":"MGI:2384163","phenotype":{"types":[{"id":"MP:0000351","label":"increased cell proliferation"}]}},{"entity":"ClinVarVariant:56687","phenotype":{"types":[{"id":"HP:0000568","label":"Microphthalmia"}]}},{"entity":"ClinVarVariant:1137","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:36494","phenotype":{"types":[{"id":"HP:0004879","label":"Intermittent hyperventilation"}]}},{"entity":"ClinVarVariant:158994","phenotype":{"types":[{"id":"HP:0002643","label":"Neonatal respiratory distress"}]}},{"entity":"ClinVarVariant:14870","phenotype":{"types":[{"id":"HP:0010049","label":"Short metacarpal"}]}},{"entity":"ClinVarVariant:54013","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:208563","phenotype":{"types":[{"id":"HP:0001397","label":"Hepatic steatosis"}]}},{"entity":"FlyBase:FBal0209552","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:211312","phenotype":{"types":[{"id":"HP:0000445","label":"Wide nose"}]}},{"entity":"ClinVarVariant:13624","phenotype":{"types":[{"id":"HP:0001257","label":"Spasticity"}]}},{"entity":"ClinVarVariant:25335","phenotype":{"types":[{"id":"HP:0012023","label":"Galactosuria"}]}},{"entity":"ClinVarVariant:21575","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"ClinVarVariant:216875","phenotype":{"types":[{"id":"HP:0002247","label":"Duodenal atresia"}]}},{"entity":"ClinVarVariant:41122","phenotype":{"types":[{"id":"HP:0000083","label":"Renal insufficiency"}]}},{"entity":"ClinVarVariant:54094","phenotype":{"types":[{"id":"HP:0002205","label":"Recurrent respiratory infections"}]}},{"entity":"ClinVarVariant:53628","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ClinVarVariant:53903","phenotype":{"types":[{"id":"HP:0003113","label":"Hypochloremia"}]}},{"entity":"ClinVarVariant:188883","phenotype":{"types":[{"id":"HP:0001947","label":"Renal tubular acidosis"}]}},{"entity":"ClinVarVariant:101165","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"ClinVarVariant:50106","phenotype":{"types":[{"id":"HP:0012469","label":"Infantile spasms"}]}},{"entity":"MGI:5588201","phenotype":{"types":[{"id":"MP:0001685","label":"abnormal endoderm development"}]}},{"entity":"ClinVarVariant:30204","phenotype":{"types":[{"id":"HP:0000577","label":"Exotropia"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00011067-WBRNAi00081161","phenotype":{"types":[{"id":"WBPhenotype:0001569","label":"body wall muscle myosin organization defective"}]}},{"entity":"MGI:2679886","phenotype":{"types":[{"id":"HP:0012535","label":"Abnormal synaptic transmission"}]}},{"entity":"dbSNP:rs7787531","phenotype":{"types":[{"id":"HP:0001347","label":"Hyperreflexia"}]}},{"entity":"ClinVarVariant:179299","phenotype":{"types":[{"id":"HP:0004309","label":"Ventricular preexcitation"}]}},{"entity":"ClinVarVariant:50854","phenotype":{"types":[{"id":"HP:0001288","label":"Gait disturbance"}]}},{"entity":"ClinVarVariant:53945","phenotype":{"types":[{"id":"HP:0002038","label":"Protein avoidance"}]}},{"entity":"ClinVarVariant:25205","phenotype":{"types":[{"id":"HP:0003355","label":"Aminoaciduria"}]}},{"entity":"ClinVarVariant:9120","phenotype":{"types":[{"id":"HP:0001631","label":"Atria septal defect"}]}},{"entity":"ClinVarVariant:135872","phenotype":{"types":[{"id":"HP:0000238","label":"Hydrocephalus"}]}},{"entity":"ClinVarVariant:56595","phenotype":{"types":[{"id":"HP:0003457","label":"EMG abnormality"}]}},{"entity":"ClinVarVariant:56615","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"FlyBase:FBal0239685","phenotype":{"types":[{"id":"FBbt:00004729PHENOTYPE","label":"Drosophila wing phenotype"}]}},{"entity":"ClinVarVariant:9551","phenotype":{"types":[{"id":"HP:0002401","label":"Stroke-like episodes"}]}},{"entity":"ClinVarVariant:49651","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"ClinVarVariant:110","phenotype":{"types":[{"id":"HP:0002321","label":"Vertigo"}]}},{"entity":"MGI:3054960","phenotype":{"types":[{"id":"MP:0001928","label":"abnormal ovulation"}]}},{"entity":"ClinVarVariant:82640","phenotype":{"types":[{"id":"HP:0005584","label":"Renal cell carcinoma"}]}},{"entity":"ClinVarVariant:2216","phenotype":{"types":[{"id":"HP:0001737","label":"Pancreatic cysts"}]}},{"entity":"ClinVarVariant:4034","phenotype":{"types":[{"id":"HP:0000158","label":"Macroglossia"}]}},{"entity":"ClinVarVariant:8963","phenotype":{"types":[{"id":"HP:0000126","label":"Hydronephrosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00002251-WBRNAi00063113","phenotype":{"types":[{"id":"WBPhenotype:0000523","label":"chemical response variant"}]}},{"entity":"AQTL:25943","phenotype":{"types":[{"id":"AQTLTrait:1034","label":"Milk fat percentage (daughter deviation)"}]}},{"entity":"ClinVarVariant:53544","phenotype":{"types":[{"id":"HP:0001408","label":"Bile duct proliferation"}]}},{"entity":"FlyBase:FBal0258455","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:189716","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:135929","phenotype":{"types":[{"id":"HP:0100615","label":"Ovarian neoplasm"}]}},{"entity":"ClinVarVariant:39","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:215576","phenotype":{"types":[{"id":"HP:0005550","label":"Chronic lymphatic leukemia"}]}},{"entity":"MGI:1856699","phenotype":{"types":[{"id":"MP:0000376","label":"folliculitis"}]}},{"entity":"ClinVarVariant:127144","phenotype":{"types":[{"id":"HP:0002078","label":"Truncal ataxia"}]}},{"entity":"MGI:1857734","phenotype":{"types":[{"id":"MP:0011084","label":"lethality at weaning, incomplete penetrance"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00018892-WBRNAi00000065","phenotype":{"types":[{"id":"WBPhenotype:0000050","label":"embryonic lethal"}]}},{"entity":"ClinVarVariant:43612","phenotype":{"types":[{"id":"HP:0001635","label":"Congestive heart failure"}]}},{"entity":"ClinVarVariant:163462","phenotype":{"types":[{"id":"HP:0002097","label":"Emphysema"}]}},{"entity":"FlyBase:FBal0128189","phenotype":{"types":[{"id":"FBcv:0000435","label":"neuroanatomy defective"}]}},{"entity":"ClinVarVariant:4387","phenotype":{"types":[{"id":"HP:0002486","label":"Myotonia"}]}},{"entity":"ClinVarVariant:95023","phenotype":{"types":[{"id":"HP:0007018","label":"Attention deficit hyperactivity disorder"}]}},{"entity":"ClinVarVariant:136194","phenotype":{"types":[{"id":"HP:0000157","label":"Abnormality of the tongue"}]}},{"entity":"ClinVarVariant:25320","phenotype":{"types":[{"id":"HP:0001252","label":"Muscular hypotonia"}]}},{"entity":"ClinVarVariant:38921","phenotype":{"types":[{"id":"HP:0001888","label":"Lymphopenia"}]}},{"entity":"ClinVarVariant:101118","phenotype":{"types":[{"id":"HP:0001373","label":"Joint dislocation"}]}},{"entity":"dbSNP:rs41643216","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:211716","phenotype":{"types":[{"id":"HP:0001249","label":"Intellectual disability"}]}},{"entity":"MGI:1857212","phenotype":{"types":[{"id":"GO:0030301PHENOTYPE","label":"cholesterol transport phenotype"}]}},{"entity":"ClinVarVariant:40562","phenotype":{"types":[{"id":"HP:0001627","label":"Abnormal heart morphology"}]}},{"entity":"ClinVarVariant:97035","phenotype":{"types":[{"id":"HP:0000023","label":"Inguinal hernia"}]}},{"entity":"ClinVarVariant:24289","phenotype":{"types":[{"id":"HP:0000613","label":"Photophobia"}]}},{"entity":"AQTL:41940","phenotype":{"types":[{"id":"AQTLTrait:1066","label":"PTA type"}]}},{"entity":"ClinVarVariant:68302","phenotype":{"types":[{"id":"HP:0009592","label":"Astrocytoma"}]}},{"entity":"dbSNP:rs5219","phenotype":{"types":[{"id":"HP:0001254","label":"Lethargy"}]}},{"entity":"ClinVarVariant:83166","phenotype":{"types":[{"id":"HP:0006740","label":"Transitional cell carcinoma of the bladder"}]}},{"entity":"FlyBase:FBal0205897","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:21164","phenotype":{"types":[{"id":"HP:0002827","label":"Hip dislocation"}]}},{"entity":"FlyBase:FBal0102923","phenotype":{"types":[{"id":"FBbt:00005177PHENOTYPE","label":"Drosophila chaeta phenotype"}]}},{"entity":"MGI:1933748","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:135879","phenotype":{"types":[{"id":"HP:0010767","label":"Sacrococcygeal pilonidal abnormality"}]}},{"entity":"ClinVarVariant:56293","phenotype":{"types":[{"id":"HP:0002059","label":"Cerebral atrophy"}]}},{"entity":"ClinVarVariant:35835","phenotype":{"types":[{"id":"HP:0002092","label":"Pulmonary hypertension"}]}},{"entity":"ClinVarVariant:39071","phenotype":{"types":[{"id":"HP:0009769","label":"Bullet-shaped phalanges of the hand"}]}},{"entity":"MGI:2668394","phenotype":{"types":[{"id":"HP:0002414","label":"Spina bifida"}]}},{"entity":"ClinVarVariant:38377","phenotype":{"types":[{"id":"HP:0002172","label":"Postural instability"}]}},{"entity":"ClinVarVariant:11846","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:53690","phenotype":{"types":[{"id":"HP:0001945","label":"Fever"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00021829-WBRNAi00004730","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:53794","phenotype":{"types":[{"id":"HP:0100598","label":"Pulmonary edema"}]}},{"entity":"MGI:4948909","phenotype":{"types":[{"id":"MP:0004952","label":"increased spleen weight"}]}},{"entity":"ClinVarVariant:204087","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"MGI:2178475","phenotype":{"types":[{"id":"HP:0011014","label":"Abnormal glucose homeostasis"}]}},{"entity":"ClinVarVariant:132749","phenotype":{"types":[{"id":"HP:0011069","label":"Increased number of teeth"}]}},{"entity":"ClinVarVariant:49681","phenotype":{"types":[{"id":"HP:0002888","label":"Ependymoma"}]}},{"entity":"MGI:3530077","phenotype":{"types":[{"id":"MP:0001513","label":"limb grasping"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00022017-WBRNAi00090877","phenotype":{"types":[{"id":"WBPhenotype:0002095","label":"lysosome-related organelle morphology variant"}]}},{"entity":"_:genid-nodeid-_:ZDB-GENE-030131-1213-ZDB-MRPHLNO-131120-6","phenotype":{"types":[{"id":"ZP:0004518","label":"abnormal(ly) immature eye"}]}},{"entity":"ClinVarVariant:14214","phenotype":{"types":[{"id":"HP:0001732","label":"Abnormality of the pancreas"}]}},{"entity":"MGI:2180880","phenotype":{"types":[{"id":"HP:0002808","label":"Kyphosis"}]}},{"entity":"ClinVarVariant:216023","phenotype":{"types":[{"id":"HP:0004322","label":"Short stature"}]}},{"entity":"MGI:1855960","phenotype":{"types":[{"id":"MP:0005075","label":"abnormal melanosome morphology"}]}},{"entity":"ClinVarVariant:53370","phenotype":{"types":[{"id":"HP:0000027","label":"Azoospermia"}]}},{"entity":"ClinVarVariant:31851","phenotype":{"types":[{"id":"HP:0000944","label":"Abnormality of the metaphyses"}]}},{"entity":"MGI:1856209","phenotype":{"types":[{"id":"HP:0001251","label":"Ataxia"}]}},{"entity":"ClinVarVariant:3187","phenotype":{"types":[{"id":"HP:0010049","label":"Short metacarpal"}]}},{"entity":"ClinVarVariant:50040","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"ClinVarVariant:190786","phenotype":{"types":[{"id":"HP:0001699","label":"Sudden death"}]}},{"entity":"ClinVarVariant:161239","phenotype":{"types":[{"id":"HP:0007293","label":"Anterior sacral meningocele"}]}},{"entity":"ClinVarVariant:29943","phenotype":{"types":[{"id":"HP:0001263","label":"Global developmental delay"}]}},{"entity":"ZFIN:ZDB-ALT-030919-2","phenotype":{"types":[{"id":"ZP:0009068","label":"abnormal(ly) disrupted spinal cord oligodendrocyte cell differentiation"}]}},{"entity":"FlyBase:FBal0239048","phenotype":{"types":[{"id":"FBcv:0001347","label":"phenotype"}]}},{"entity":"ClinVarVariant:14718","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:40186","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"ClinVarVariant:156282","phenotype":{"types":[{"id":"HP:0001337","label":"Tremor"}]}},{"entity":"MGI:3845227","phenotype":{"types":[{"id":"HP:0005563","label":"Decreased numbers of nephrons"}]}},{"entity":"ClinVarVariant:53858","phenotype":{"types":[{"id":"HP:0100724","label":"Hypercoagulability"}]}},{"entity":"FlyBase:FBal0207413","phenotype":{"types":[{"id":"FBcv:0000349","label":"viable"}]}},{"entity":"ClinVarVariant:4443","phenotype":{"types":[{"id":"HP:0008682","label":"Acute tubular necrosis"}]}},{"entity":"ClinVarVariant:13503","phenotype":{"types":[{"id":"HP:0002171","label":"Gliosis"}]}},{"entity":"ClinVarVariant:8189","phenotype":{"types":[{"id":"HP:0002196","label":"Myelopathy"}]}},{"entity":"ClinVarVariant:38980","phenotype":{"types":[{"id":"HP:0003458","label":"EMG: myopathic abnormalities"}]}},{"entity":"ClinVarVariant:136167","phenotype":{"types":[{"id":"HP:0001578","label":"Hypercortisolism"}]}},{"entity":"ClinVarVariant:13960","phenotype":{"types":[{"id":"HP:0001640","label":"Cardiomegaly"}]}},{"entity":"ClinVarVariant:21166","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:1333","phenotype":{"types":[{"id":"HP:0000601","label":"Hypotelorism"}]}},{"entity":"MGI:4429385","phenotype":{"types":[{"id":"MP:0001364","label":"decreased anxiety-related response"}]}},{"entity":"ClinVarVariant:53992","phenotype":{"types":[{"id":"HP:0002090","label":"Pneumonia"}]}},{"entity":"ClinVarVariant:41462","phenotype":{"types":[{"id":"HP:0000473","label":"Torticollis"}]}},{"entity":"MGI:3716074","phenotype":{"types":[{"id":"MP:0005332","label":"abnormal amino acid level"}]}},{"entity":"ClinVarVariant:180305","phenotype":{"types":[{"id":"HP:0001519","label":"Disproportionate tall stature"}]}},{"entity":"ClinVarVariant:48806","phenotype":{"types":[{"id":"HP:0009720","label":"Adenoma sebaceum"}]}},{"entity":"FlyBase:FBal0183239","phenotype":{"types":[{"id":"FBbt:00005156PHENOTYPE","label":"Drosophila mechanosensory sensory organ phenotype"}]}},{"entity":"ClinVarVariant:49247","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"ClinVarVariant:35753","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"MGI:1931048","phenotype":{"types":[{"id":"MP:0005325","label":"abnormal renal glomerulus morphology"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006917-WBRNAi00040864","phenotype":{"types":[{"id":"WBPhenotype:0000689","label":"maternal sterile"}]}},{"entity":"ClinVarVariant:21779","phenotype":{"types":[{"id":"HP:0002411","label":"Myokymia"}]}},{"entity":"ClinVarVariant:127349","phenotype":{"types":[{"id":"HP:0000246","label":"Sinusitis"}]}},{"entity":"ClinVarVariant:21218","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"WormBase:WBVar00143078","phenotype":{"types":[{"id":"WBPhenotype:0001652","label":"anchor cell invasion variant"}]}},{"entity":"ClinVarVariant:49810","phenotype":{"types":[{"id":"HP:0000169","label":"Gingival fibromatosis"}]}},{"entity":"ClinVarVariant:53356","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"ClinVarVariant:17272","phenotype":{"types":[{"id":"HP:0002273","label":"Tetraparesis"}]}},{"entity":"ClinVarVariant:211467","phenotype":{"types":[{"id":"HP:0001156","label":"Brachydactyly syndrome"}]}},{"entity":"ClinVarVariant:10204","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:6542","phenotype":{"types":[{"id":"HP:0001805","label":"Thick nail"}]}},{"entity":"ClinVarVariant:10822","phenotype":{"types":[{"id":"HP:0002757","label":"Recurrent fractures"}]}},{"entity":"ClinVarVariant:5449","phenotype":{"types":[{"id":"HP:0002671","label":"Basal cell carcinoma"}]}},{"entity":"ClinVarVariant:180392","phenotype":{"types":[{"id":"HP:0011034","label":"Amyloidosis"}]}},{"entity":"ClinVarVariant:5905","phenotype":{"types":[{"id":"HP:0002093","label":"Respiratory insufficiency"}]}},{"entity":"ClinVarVariant:41187","phenotype":{"types":[{"id":"HP:0001733","label":"Pancreatitis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004506-WBRNAi00078787","phenotype":{"types":[{"id":"WBPhenotype:0001171","label":"shortened life span"}]}},{"entity":"ClinVarVariant:21451","phenotype":{"types":[{"id":"HP:0000508","label":"Ptosis"}]}},{"entity":"ClinVarVariant:2628","phenotype":{"types":[{"id":"HP:0002311","label":"Incoordination"}]}},{"entity":"ClinVarVariant:50060","phenotype":{"types":[{"id":"HP:0000957","label":"Cafe-au-lait spot"}]}},{"entity":"ClinVarVariant:12965","phenotype":{"types":[{"id":"HP:0003768","label":"Periodic paralysis"}]}},{"entity":"ClinVarVariant:2453","phenotype":{"types":[{"id":"HP:0001324","label":"Muscle weakness"}]}},{"entity":"ClinVarVariant:210427","phenotype":{"types":[{"id":"HP:0005599","label":"Hypopigmentation of hair"}]}},{"entity":"ClinVarVariant:53863","phenotype":{"types":[{"id":"HP:0010943","label":"Echogenic fetal bowel"}]}},{"entity":"ClinVarVariant:215894","phenotype":{"types":[{"id":"HP:0000012","label":"Urinary urgency"}]}},{"entity":"ClinVarVariant:9714","phenotype":{"types":[{"id":"HP:0001999","label":"Abnormal facial shape"}]}},{"entity":"MGI:3836429","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:8061","phenotype":{"types":[{"id":"HP:0006443","label":"Patellar aplasia"}]}},{"entity":"ClinVarVariant:217068","phenotype":{"types":[{"id":"HP:0007440","label":"Generalized hyperpigmentation"}]}},{"entity":"ClinVarVariant:54053","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:209164","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"FlyBase:FBal0195554","phenotype":{"types":[{"id":"FBbt:00001311PHENOTYPE","label":"interface glial cell phenotype"}]}},{"entity":"FlyBase:FBal0209714","phenotype":{"types":[{"id":"FBcv:0002039","label":"some die during pupal stage"}]}},{"entity":"FlyBase:FBal0091132","phenotype":{"types":[{"id":"FBbt:00004642PHENOTYPE","label":"Drosophila tibia phenotype"}]}},{"entity":"ClinVarVariant:189261","phenotype":{"types":[{"id":"HP:0001284","label":"Areflexia"}]}},{"entity":"ClinVarVariant:10915","phenotype":{"types":[{"id":"HP:0100543","label":"Cognitive impairment"}]}},{"entity":"ClinVarVariant:39848","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"dbSNP:rs110754910","phenotype":{"types":[{"id":"AQTLTrait:1049","label":"Body weight (200 day weaning)"}]}},{"entity":"ClinVarVariant:93724","phenotype":{"types":[{"id":"HP:0006979","label":"Sleep-wake cycle disturbance"}]}},{"entity":"ClinVarVariant:25231","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"MGI:3656024","phenotype":{"types":[{"id":"MP:0000228","label":"abnormal thrombopoiesis"}]}},{"entity":"ClinVarVariant:5312","phenotype":{"types":[{"id":"HP:0000639","label":"Nystagmus"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004188-WBRNAi00095757","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:68288","phenotype":{"types":[{"id":"HP:0001874","label":"Abnormality of neutrophils"}]}},{"entity":"ClinVarVariant:53660","phenotype":{"types":[{"id":"HP:0011993","label":"Impaired neutrophil bactericidal activity"}]}},{"entity":"ClinVarVariant:8184","phenotype":{"types":[{"id":"HP:0003095","label":"Septic arthritis"}]}},{"entity":"ClinVarVariant:30988","phenotype":{"types":[{"id":"HP:0001845","label":"Overlapping toe"}]}},{"entity":"ZFIN:ZDB-ALT-050916-14","phenotype":{"types":[{"id":"ZP:0004993","label":"abnormal(ly) constricted heart"}]}},{"entity":"ClinVarVariant:53943","phenotype":{"types":[{"id":"HP:0000010","label":"Recurrent urinary tract infections"}]}},{"entity":"MGI:5466366","phenotype":{"types":[{"id":"MP:0001513","label":"limb grasping"}]}},{"entity":"ClinVarVariant:53935","phenotype":{"types":[{"id":"HP:0001824","label":"Weight loss"}]}},{"entity":"ClinVarVariant:56613","phenotype":{"types":[{"id":"HP:0000316","label":"Hypertelorism"}]}},{"entity":"ClinVarVariant:183678","phenotype":{"types":[{"id":"HP:0000028","label":"Cryptorchidism"}]}},{"entity":"ClinVarVariant:16879","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}},{"entity":"ClinVarVariant:38752","phenotype":{"types":[{"id":"HP:0000519","label":"Congenital cataract"}]}},{"entity":"ClinVarVariant:182386","phenotype":{"types":[{"id":"HP:0000175","label":"Cleft palate"}]}},{"entity":"ClinVarVariant:65739","phenotype":{"types":[{"id":"HP:0000691","label":"Microdontia"}]}},{"entity":"ClinVarVariant:53841","phenotype":{"types":[{"id":"HP:0004325","label":"Decreased body weight"}]}},{"entity":"ClinVarVariant:66439","phenotype":{"types":[{"id":"HP:0011441","label":"Abnormality of the medulla oblongata"}]}},{"entity":"ClinVarVariant:2259","phenotype":{"types":[{"id":"HP:0001287","label":"Meningitis"}]}},{"entity":"ClinVarVariant:1703","phenotype":{"types":[{"id":"HP:0002240","label":"Hepatomegaly"}]}},{"entity":"_:genid1976040","phenotype":{"types":[{"id":"ZP:0002310","label":"abnormal(ly) circling whole organism"}]}},{"entity":"dbSNP:rs12386026","phenotype":{"types":[{"id":"HP:0006516","label":"Hypersensitivity pneumonitis"}]}},{"entity":"MGI:3761621","phenotype":{"types":[{"id":"HP:0001744","label":"Splenomegaly"}]}},{"entity":"ClinVarVariant:211746","phenotype":{"types":[{"id":"HP:0002650","label":"Scoliosis"}]}},{"entity":"ClinVarVariant:158392","phenotype":{"types":[{"id":"HP:0004209","label":"Clinodactyly of the 5th finger"}]}},{"entity":"ClinVarVariant:12641","phenotype":{"types":[{"id":"HP:0000819","label":"Diabetes mellitus"}]}},{"entity":"MGI:4432238","phenotype":{"types":[{"id":"MP:0004889","label":"increased energy expenditure"}]}},{"entity":"ClinVarVariant:217052","phenotype":{"types":[{"id":"HP:0100697","label":"Neurofibrosarcoma"}]}},{"entity":"ClinVarVariant:11129","phenotype":{"types":[{"id":"HP:0005549","label":"Congenital neutropenia"}]}},{"entity":"ClinVarVariant:56034","phenotype":{"types":[{"id":"HP:0000815","label":"Hypergonadotropic hypogonadism"}]}},{"entity":"ClinVarVariant:6286","phenotype":{"types":[{"id":"HP:0000925","label":"Abnormality of the vertebral column"}]}},{"entity":"ClinVarVariant:9960","phenotype":{"types":[{"id":"HP:0004936","label":"Venous thrombosis"}]}},{"entity":"ClinVarVariant:64779","phenotype":{"types":[{"id":"HP:0009722","label":"Dental enamel pits"}]}},{"entity":"ClinVarVariant:56635","phenotype":{"types":[{"id":"HP:0000479","label":"Abnormality of the retina"}]}},{"entity":"MGI:2158457","phenotype":{"types":[{"id":"MP:0000527","label":"abnormal kidney development"}]}},{"entity":"ClinVarVariant:100671","phenotype":{"types":[{"id":"HP:0004719","label":"Hyperechogenic kidneys"}]}},{"entity":"ClinVarVariant:12791","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:101135","phenotype":{"types":[{"id":"HP:0000212","label":"Gingival overgrowth"}]}},{"entity":"ClinVarVariant:189852","phenotype":{"types":[{"id":"HP:0002384","label":"Focal seizures with impairment of consciousness or awareness"}]}},{"entity":"AQTL:20678","phenotype":{"types":[{"id":"AQTLTrait:10","label":"Backfat at last lumbar"}]}},{"entity":"ClinVarVariant:13340","phenotype":{"types":[{"id":"HP:0004808","label":"Acute myeloid leukemia"}]}},{"entity":"ClinVarVariant:40490","phenotype":{"types":[{"id":"HP:0100495","label":"Mastocytosis"}]}},{"entity":"ClinVarVariant:94601","phenotype":{"types":[{"id":"HP:0003560","label":"Muscular dystrophy"}]}},{"entity":"WormBase:WBVar00531947","phenotype":{"types":[{"id":"WBPhenotype:0000138","label":"lipid composition variant"}]}},{"entity":"MGI:3712283","phenotype":{"types":[{"id":"MP:0006316","label":"increased urine sodium level"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00017983-WBRNAi00075550","phenotype":{"types":[{"id":"WBPhenotype:0000032","label":"sick"}]}},{"entity":"ClinVarVariant:44631","phenotype":{"types":[{"id":"HP:0000179","label":"Thick lower lip vermilion"}]}},{"entity":"MGI:5317762","phenotype":{"types":[{"id":"HP:0000204","label":"Cleft upper lip"}]}},{"entity":"MGI:2153094","phenotype":{"types":[{"id":"HP:0001397","label":"Hepatic steatosis"}]}},{"entity":"MGI:5467564","phenotype":{"types":[{"id":"MP:0002083","label":"premature death"}]}},{"entity":"ClinVarVariant:132733","phenotype":{"types":[{"id":"HP:0100777","label":"Exostoses"}]}},{"entity":"ClinVarVariant:53794","phenotype":{"types":[{"id":"HP:0002105","label":"Hemoptysis"}]}},{"entity":"ClinVarVariant:1568","phenotype":{"types":[{"id":"HP:0002014","label":"Diarrhea"}]}},{"entity":"ClinVarVariant:5502","phenotype":{"types":[{"id":"HP:0200094","label":"Frontal open bite"}]}},{"entity":"MGI:3043520","phenotype":{"types":[{"id":"MP:0004952","label":"increased spleen weight"}]}},{"entity":"MGI:2157350","phenotype":{"types":[{"id":"GO:0030900PHENOTYPE","label":"forebrain development phenotype"}]}},{"entity":"ClinVarVariant:17189","phenotype":{"types":[{"id":"HP:0000768","label":"Pectus carinatum"}]}},{"entity":"ClinVarVariant:18025","phenotype":{"types":[{"id":"HP:0004850","label":"Recurrent deep vein thrombosis"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00006975-WBRNAi00081919","phenotype":{"types":[{"id":"WBPhenotype:0001595","label":"somatic transgene silencing variant"}]}},{"entity":"ClinVarVariant:100719","phenotype":{"types":[{"id":"HP:0001250","label":"Seizures"}]}},{"entity":"ClinVarVariant:9454","phenotype":{"types":[{"id":"HP:0000529","label":"Progressive visual loss"}]}},{"entity":"ClinVarVariant:53366","phenotype":{"types":[{"id":"HP:0002630","label":"Fat malabsorption"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00004453-WBRNAi00072949","phenotype":{"types":[{"id":"WBPhenotype:0000062","label":"lethal"}]}},{"entity":"ClinVarVariant:204127","phenotype":{"types":[{"id":"HP:0001513","label":"Obesity"}]}},{"entity":"ClinVarVariant:1236","phenotype":{"types":[{"id":"HP:0001270","label":"Motor delay"}]}},{"entity":"ClinVarVariant:48912","phenotype":{"types":[{"id":"HP:0002086","label":"Abnormality of the respiratory system"}]}},{"entity":"ClinVarVariant:8212","phenotype":{"types":[{"id":"HP:0001000","label":"Abnormality of skin pigmentation"}]}},{"entity":"ClinVarVariant:30180","phenotype":{"types":[{"id":"HP:0000272","label":"Malar flattening"}]}},{"entity":"http://www.monarchinitiative.org/_WBGene00007030-WBRNAi00026587","phenotype":{"types":[{"id":"HP:0001508","label":"Failure to thrive"}]}}],"schema":"phenopacket-level-1"},"params":{"q":"*:*","fq":"(subject_closure:\"HP:0000739\" OR subject_closure:\"MP:0001363\")","personality":"variant_phenotype","showEmptyFields":false},"name":"Monarch Application","date":"Sun Jun 26 2016 12:08:27 GMT-0700 (PDT)"}
\ No newline at end of file
diff -r 000000000000 -r 850bb90bd667 test-data/variants-for-disease.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/variants-for-disease.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,316 @@
+ClinVarVariant:39148 NM_198578.3(LRRK2):c.2264C>T (p.Pro755Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7051 NM_004562.2(PARK2):c.633A>T (p.Lys211Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1936 NM_198578.3(LRRK2):c.4321C>G (p.Arg1441Gly) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4810 NM_012179.3(FBXO7):c.1144+1G>T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:260300 autosomal recessive early-onset Parkinson disease 15 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39147 NM_198578.3(LRRK2):c.225G>A (p.Ala75=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39234 NM_198578.3(LRRK2):c.7155A>G (p.Gly2385=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2412 NM_005216.4(DDOST):c.*807_*5409del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7050 NM_004562.2(PARK2):c.823C>T (p.Arg275Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9695 m.14319T>C NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39128 NM_198578.3(LRRK2):c.1000G>A (p.Glu334Lys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39215 NM_198578.3(LRRK2):c.5620G>T (p.Glu1874Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39195 NM_198578.3(LRRK2):c.4793T>A (p.Val1598Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:209135 NM_022089.3(ATP13A2):c.348-9_351del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4809 NM_012179.3(FBXO7):c.1492C>T (p.Arg498Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:260300 autosomal recessive early-onset Parkinson disease 15 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39214 NM_198578.3(LRRK2):c.5610G>T (p.Leu1870Phe) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:143196 NM_022089.3(ATP13A2):c.490C>T (p.Arg164Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39194 NM_198578.3(LRRK2):c.4666C>A (p.Leu1556Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7042 NM_004562.2(PARK2):c.1358G>A (p.Trp453Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9695 m.14319T>C NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39213 NM_198578.3(LRRK2):c.5606T>C (p.Met1869Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39193 NM_198578.3(LRRK2):c.4624C>T (p.Pro1542Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+NCBIGene:677662 PARK12 NCBITaxon:9606 Homo sapiens RO:0002326 contributes to NCBIGene:677662 PARK12 ECO:0000177 genomic context evidence http://data.monarchinitiative.org/ttl/omim.ttl direct
+ClinVarVariant:39192 NM_198578.3(LRRK2):c.457T>C (p.Leu153=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39212 NM_198578.3(LRRK2):c.5605A>G (p.Met1869Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+NCBIGene:5072 PARK3 NCBITaxon:9606 Homo sapiens RO:0002326 contributes to NCBIGene:5072 PARK3 ECO:0000177 genomic context evidence http://data.monarchinitiative.org/ttl/omim.ttl direct
+ClinVarVariant:4808 NM_012179.3(FBXO7):c.1132C>G (p.Arg378Gly) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:260300 autosomal recessive early-onset Parkinson disease 15 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39191 NM_198578.3(LRRK2):c.4541G>A (p.Arg1514Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30371 NM_003560.2(PLA2G6):c.991G>T (p.Asp331Tyr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:612953 Parkinson Disease 14, Autosomal Recessive http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39238 NM_198578.3(LRRK2):c.7190T= (p.Met2397=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7053 NM_004562.2(PARK2):c.7+1G>T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:50354 NM_004562.2(PARK2):c.1292G>T (p.Cys431Phe) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2404 NM_032409.2(PINK1):c.926G>A (p.Gly309Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39237 NM_198578.3(LRRK2):c.7186_7187dupGT (p.Met2397Terfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1937 NM_198578.3(LRRK2):c.5096A>G (p.Tyr1699Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4811 NM_012179.3(FBXO7):c.65C>T (p.Thr22Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:260300 autosomal recessive early-onset Parkinson disease 15 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7052 PARK2, 1-BP DEL, 1072T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39149 NM_198578.3(LRRK2):c.2378G>T (p.Arg793Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39236 NM_198578.3(LRRK2):c.7183G>A (p.Glu2395Lys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:8113 NM_002973.3(ATXN2):c.496_498CAG(15_24) (p.Gln188_Pro189insGlnGln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39235 NM_198578.3(LRRK2):c.7168G>A (p.Val2390Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:12298 NM_004181.4(UCHL1):c.53C>A (p.Ser18Tyr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613643 Parkinson Disease 5, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39211 NM_198578.3(LRRK2):c.546A>G (p.Lys182=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7048 PARK2, 1-BP DEL, 255A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4342 NM_013247.4(HTRA2):c.421G>T (p.Ala141Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:12297 NM_004181.4(UCHL1):c.279C>G (p.Ile93Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613643 Parkinson Disease 5, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7050 NM_004562.2(PARK2):c.823C>T (p.Arg275Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9726 m.3397A>G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7055 PARK2, EX5-6 DEL NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39210 NM_198578.3(LRRK2):c.5467C>A (p.Gln1823Lys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39190 NM_198578.3(LRRK2):c.4448G>A (p.Arg1483Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39239 NM_198578.3(LRRK2):c.7224G>A (p.Met2408Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:29936 NM_012084.3(GLUD2):c.1492T>G (p.Ser498Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4885 FGF20, 951C/T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1939 NM_198578.3(LRRK2):c.3364A>G (p.Ile1122Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39233 NM_198578.3(LRRK2):c.713A>T (p.Asn238Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39146 NM_198578.3(LRRK2):c.2167A>G (p.Ile723Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7035 NM_004562.2(PARK2):c.413-?_534+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:98243 NM_016835.4(MAPT):c.1838_1840delATA (p.Asn613del) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9579 m.8344A>G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7064 NM_007262.4(PARK7):c.497T>C (p.Leu166Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39232 NM_198578.3(LRRK2):c.7067C>T (p.Thr2356Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39145 NM_198578.3(LRRK2):c.2147C>T (p.Ala716Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4295 NM_001005741.2(GBA):c.1504C>T (p.Arg502Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:18181 NM_000669.4(ADH1C):c.232G>T (p.Gly78Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39231 NM_198578.3(LRRK2):c.683G>C (p.Cys228Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39144 NM_198578.3(LRRK2):c.2134A>G (p.Met712Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7040 NM_004562.2(PARK2):c.8-?_171+?del NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:39143 NM_198578.3(LRRK2):c.2022A>C (p.Val674=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7043 NM_004562.2(PARK2):c.483A>T (p.Lys161Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39230 NM_198578.3(LRRK2):c.6782A>T (p.Asn2261Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:6204 NM_003560.2(PLA2G6):c.2239C>T (p.Arg747Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:612953 Parkinson Disease 14, Autosomal Recessive http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2409 NM_032409.2(PINK1):c.1570_1573dupTTAG (p.Asp525Valfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39221 NM_198578.3(LRRK2):c.6241A>G (p.Asn2081Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2407 NM_032409.2(PINK1):c.736C>T (p.Arg246Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39134 NM_198578.3(LRRK2):c.149A>G (p.His50Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:6203 NM_003560.2(PLA2G6):c.2222G>A (p.Arg741Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:612953 Parkinson Disease 14, Autosomal Recessive http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30583 NM_013247.4(HTRA2):c.427C>G (p.Pro143Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39132 NM_198578.3(LRRK2):c.1383T= (p.Ser461=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2408 NM_032409.2(PINK1):c.1040T>C (p.Leu347Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39220 NM_198578.3(LRRK2):c.6187_6191delCTCTA (p.Leu2063Terfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39133 NM_198578.3(LRRK2):c.1464A>T (p.Leu488=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:56171 NM_015268.3(DNAJC13):c.2564A>G (p.Asn855Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39243 NM_198578.3(LRRK2):c.825T= (p.His275=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:755 NM_015575.3(GIGYF2):c.1818C>G (p.Asp606Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39156 NM_198578.3(LRRK2):c.2857T>C (p.Leu953=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:14009 SNCA, TRIPLICATION NCBITaxon:9606 Homo sapiens OMIM:168601 autosomal dominant Parkinson disease 1 http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:7046 NM_004562.2(PARK2):c.635G>A (p.Cys212Tyr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:6144 NR_002717.2(ATXN8OS):n.1103_1105CTG(15_40) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+NCBIGene:100359403 PARK16 NCBITaxon:9606 Homo sapiens RO:0002326 contributes to NCBIGene:100359403 PARK16 ECO:0000177 genomic context evidence http://data.monarchinitiative.org/ttl/omim.ttl direct
+ClinVarVariant:1942 NM_198578.3(LRRK2):c.4322G>A (p.Arg1441His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:29685 NM_001044.4(SLC6A3):c.1269+1G>A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613135 Parkinsonism-Dystonia, Infantile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9054 NM_021074.4(NDUFV2):c.86T>C (p.Val29Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39155 NM_198578.3(LRRK2):c.2830G>T (p.Asp944Tyr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:754 NM_015575.3(GIGYF2):c.1370A>C (p.Asn457Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39242 NM_198578.3(LRRK2):c.7468delC (p.Gln2490Asnfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41223 NM_004562.2(PARK2):c.500G>A (p.Ser167Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:757 NM_015575.3(GIGYF2):c.1262A>G (p.Lys421Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39158 NM_198578.3(LRRK2):c.2918G>A (p.Ser973Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41222 NM_004562.2(PARK2):c.1180G>A (p.Asp394Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:66098 NM_022089.3(ATP13A2):c.2561T>G (p.Met854Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39167 NM_198578.3(LRRK2):c.356T>C (p.Leu119Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2405 NM_032409.2(PINK1):c.813C>A (p.His271Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2414 NM_032409.2(PINK1):c.650C>A (p.Ala217Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41223 NM_004562.2(PARK2):c.500G>A (p.Ser167Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39169 NM_198578.3(LRRK2):c.3647A>G (p.His1216Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7038 NM_004562.2(PARK2):c.245C>A (p.Ala82Glu) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:97017 NM_001044.4(SLC6A3):c.671T>C (p.Leu224Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613135 Parkinsonism-Dystonia, Infantile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:97000 NM_000345.3(SNCA):c.152G>A (p.Gly51Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168601 autosomal dominant Parkinson disease 1 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2415 NM_032409.2(PINK1):c.1366C>T (p.Gln456Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2412 NM_005216.4(DDOST):c.*807_*5409del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:60700 NM_007262.4(PARK7):c.-24+75_-24+92dup NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39165 NM_198578.3(LRRK2):c.3451G>A (p.Ala1151Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96731 NM_198578.3(LRRK2):c.7300A>G (p.Ile2434Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:216934 NM_001103146.1(GIGYF2):c.2378C>T (p.Ala793Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2413 NM_032409.2(PINK1):c.938C>T (p.Thr313Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41221 NM_004562.2(PARK2):c.1138G>C (p.Val380Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39166 NM_198578.3(LRRK2):c.3494T>C (p.Leu1165Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41220 NM_004562.2(PARK2):c.1096C>T (p.Arg366Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4342 NM_013247.4(HTRA2):c.421G>T (p.Ala141Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2410 PINK1, 3-BP INS, 1602CAA NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7065 NM_007262.4(PARK7):c.78G>A (p.Met26Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7036 NM_004562.2(PARK2):c.719C>G (p.Thr240Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39163 NM_198578.3(LRRK2):c.3333G>T (p.Gln1111His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2405 NM_032409.2(PINK1):c.813C>A (p.His271Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39246 NM_198578.3(LRRK2):c.936G>T (p.Ala312=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:14009 SNCA, TRIPLICATION NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605543 Parkinson Disease 4, Autosomal Dominant http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39159 NM_198578.3(LRRK2):c.3018A>G (p.Ile1006Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39244 NM_198578.3(LRRK2):c.867C= (p.Asn289=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:756 NM_015575.3(GIGYF2):c.832A>G (p.Ile278Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39157 NM_198578.3(LRRK2):c.28G>A (p.Glu10Lys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2404 NM_032409.2(PINK1):c.926G>A (p.Gly309Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39245 NM_198578.3(LRRK2):c.894T>C (p.Ala298=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:97016 NM_001044.4(SLC6A3):c.1031+1G>A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613135 Parkinsonism-Dystonia, Infantile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:3551 NM_004993.5(ATXN3):c.892_894CAG(8_36) (p.Gln298_Gln305=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39168 NM_198578.3(LRRK2):c.3574A>G (p.Ile1192Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:66099 NM_022089.3(ATP13A2):c.2629G>A (p.Gly877Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4341 NM_013247.4(HTRA2):c.1195G>A (p.Gly399Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9571 m.15965A>G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2411 NM_032409.2(PINK1):c.836G>A (p.Arg279His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2413 NM_032409.2(PINK1):c.938C>T (p.Thr313Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39164 NM_198578.3(LRRK2):c.3342A>G (p.Leu1114=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96729 NM_032409.2(PINK1):c.923T>A (p.Leu308Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39161 NM_198578.3(LRRK2):c.3200G>A (p.Arg1067Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39189 NM_198578.3(LRRK2):c.4402A>G (p.Lys1468Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39209 NM_198578.3(LRRK2):c.5457T>C (p.Gly1819=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39160 NM_198578.3(LRRK2):c.3021T= (p.Ser1007=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9559 m.15950G>A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7044 PARK2, 1-BP DEL, 202A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39206 NM_198578.3(LRRK2):c.5183G>A (p.Arg1728His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30368 PLA2G6, PHE72LEU NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:612953 Parkinson Disease 14, Autosomal Recessive http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39186 NM_198578.3(LRRK2):c.4337C>T (p.Pro1446Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7052 PARK2, 1-BP DEL, 1072T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39162 NM_198578.3(LRRK2):c.3287C>G (p.Ser1096Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96730 NM_198578.3(LRRK2):c.2352C>A (p.Ser784Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39278 NM_198578.3(LRRK2):c.6523G>C (p.Asp2175His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7035 NM_004562.2(PARK2):c.413-?_534+?del NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:39208 NM_198578.3(LRRK2):c.5385G>T (p.Leu1795Phe) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30583 NM_013247.4(HTRA2):c.427C>G (p.Pro143Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39188 NM_198578.3(LRRK2):c.4364_4365delAT (p.Asp1455Glyfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41221 NM_004562.2(PARK2):c.1138G>C (p.Val380Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39187 NM_198578.3(LRRK2):c.4348G>A (p.Val1450Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96728 NM_032409.2(PINK1):c.644C>T (p.Pro215Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:38301 NM_001005741.2(GBA):c.1226A>C (p.Asn409Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39183 NM_198578.3(LRRK2):c.4309A>C (p.Asn1437His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2406 NM_032409.2(PINK1):c.1311G>A (p.Trp437Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39184 NM_198578.3(LRRK2):c.4323C>T (p.Arg1441=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30366 NM_003560.2(PLA2G6):c.1904G>A (p.Arg635Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:612953 Parkinson Disease 14, Autosomal Recessive http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39204 NM_198578.3(LRRK2):c.5173C>T (p.Arg1725Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96727 NM_018206.4(VPS35):c.1576C>T (p.Arg526Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39185 NM_198578.3(LRRK2):c.4324G>C (p.Ala1442Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30367 NM_003560.2(PLA2G6):c.1354C>T (p.Gln452Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:612953 Parkinson Disease 14, Autosomal Recessive http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39205 NM_198578.3(LRRK2):c.5174G>A (p.Arg1725Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39181 NM_198578.3(LRRK2):c.4269G>A (p.Lys1423=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7046 NM_004562.2(PARK2):c.635G>A (p.Cys212Tyr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2414 NM_032409.2(PINK1):c.650C>A (p.Ala217Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39201 NM_198578.3(LRRK2):c.4939T>A (p.Ser1647Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:189240 NM_032409.2(PINK1):c.620delG (p.Arg207Glnfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7047 NM_004562.2(PARK2):c.167T>A (p.Val56Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:183259 NM_032409.2(PINK1):c.799C>T (p.Gln267Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39202 NM_198578.3(LRRK2):c.4959A>G (p.Leu1653=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39182 NM_198578.3(LRRK2):c.4290C>T (p.Ala1430=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4288 NM_001005741.2(GBA):c.1448T>C (p.Leu483Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7048 PARK2, 1-BP DEL, 255A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39203 NM_198578.3(LRRK2):c.5163A>G (p.Ser1721=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39151 NM_198578.3(LRRK2):c.2481T>C (p.Ser827=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+dbSNP:rs34778348 rs34778348-? NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2408 NM_032409.2(PINK1):c.1040T>C (p.Leu347Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2410 PINK1, 3-BP INS, 1602CAA NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1936 NM_198578.3(LRRK2):c.4321C>G (p.Arg1441Gly) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:39152 NM_198578.3(LRRK2):c.2611A>G (p.Lys871Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30833 NM_022089.3(ATP13A2):c.1101_1102dupGA (p.Thr368Argfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:14008 NM_000345.3(SNCA):c.88G>C (p.Ala30Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168601 autosomal dominant Parkinson disease 1 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39240 NM_198578.3(LRRK2):c.7397T>A (p.Leu2466His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41220 NM_004562.2(PARK2):c.1096C>T (p.Arg366Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39142 NM_198578.3(LRRK2):c.1987T>C (p.Ser663Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1221 NM_022089.3(ATP13A2):c.1510G>C (p.Gly504Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7051 NM_004562.2(PARK2):c.633A>T (p.Lys211Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:97018 NM_001044.4(SLC6A3):c.1561C>T (p.Arg521Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613135 Parkinsonism-Dystonia, Infantile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39140 NM_198578.3(LRRK2):c.1674G= (p.Gly558=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39141 NM_198578.3(LRRK2):c.1847A>G (p.Lys616Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:60700 NM_007262.4(PARK7):c.-24+75_-24+92dup NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1220 ATP13A2, 22-BP DUP NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39153 NM_198578.3(LRRK2):c.2769G>C (p.Gln923His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30834 NM_022089.3(ATP13A2):c.2552_2553delTT (p.Phe851Cysfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7050 NM_004562.2(PARK2):c.823C>T (p.Arg275Trp) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:39154 NM_198578.3(LRRK2):c.2789A>G (p.Gln930Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:753 NM_015575.3(GIGYF2):c.167A>G (p.Asn56Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39241 NM_198578.3(LRRK2):c.7435A>G (p.Asn2479Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1941 NM_198578.3(LRRK2):c.6059T>C (p.Ile2020Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:12298 NM_004181.4(UCHL1):c.53C>A (p.Ser18Tyr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7064 NM_007262.4(PARK7):c.497T>C (p.Leu166Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39176 NM_198578.3(LRRK2):c.4111A>G (p.Ile1371Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39175 NM_198578.3(LRRK2):c.3974G>A (p.Arg1325Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7065 NM_007262.4(PARK7):c.78G>A (p.Met26Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39177 NM_198578.3(LRRK2):c.4125C>A (p.Asp1375Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30072 NM_198241.2(EIF4G1):c.3614G>A (p.Arg1205His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:56171 NM_015268.3(DNAJC13):c.2564A>G (p.Asn855Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:616361 Parkinson Disease 21 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:162095 NM_000345.3(SNCA):c.150T>G (p.His50Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168601 autosomal dominant Parkinson disease 1 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7041 NM_004562.2(PARK2):c.872-?_1083+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9449 NM_003194.4(TBP):c.172_174CAG(25_42) (p.Gln95(25_42)) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30073 NM_198241.2(EIF4G1):c.1505C>T (p.Ala502Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39178 NM_198578.3(LRRK2):c.4193G>A (p.Arg1398His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7048 PARK2, 1-BP DEL, 255A NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:7066 NM_007262.4(PARK7):c.446A>C (p.Asp149Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:14007 NM_000345.3(SNCA):c.157G>A (p.Ala53Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168601 autosomal dominant Parkinson disease 1 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39179 NM_198578.3(LRRK2):c.4229C>T (p.Thr1410Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39150 NM_198578.3(LRRK2):c.2428A>G (p.Ile810Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7067 NM_007262.4(PARK7):c.192G>C (p.Glu64Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39171 NM_198578.3(LRRK2):c.3683G>C (p.Ser1228Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7036 NM_004562.2(PARK2):c.719C>G (p.Thr240Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7037 NM_004562.2(PARK2):c.931C>T (p.Gln311Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7038 NM_004562.2(PARK2):c.245C>A (p.Ala82Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7047 NM_004562.2(PARK2):c.167T>A (p.Val56Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39173 NM_198578.3(LRRK2):c.3784C>G (p.Pro1262Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4341 NM_013247.4(HTRA2):c.1195G>A (p.Gly399Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30196 NM_018206.4(VPS35):c.1858G>A (p.Asp620Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:614203 Parkinson Disease 17 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:183259 NM_032409.2(PINK1):c.799C>T (p.Gln267Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39174 NM_198578.3(LRRK2):c.3960G>T (p.Arg1320Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7063 NC_000001.10:g.(8018845_8022846)_(8037799_8044954)del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:209136 NM_022089.3(ATP13A2):c.943G>A (p.Gly315Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39216 NM_198578.3(LRRK2):c.5822G>A (p.Arg1941His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39196 NM_198578.3(LRRK2):c.4838T>C (p.Val1613Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39129 NM_198578.3(LRRK2):c.1088A>G (p.Asn363Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7034 NM_004562.2(PARK2):c.172-?_871+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:50354 NM_004562.2(PARK2):c.1292G>T (p.Cys431Phe) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7063 NC_000001.10:g.(8018845_8022846)_(8037799_8044954)del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39217 NM_198578.3(LRRK2):c.6016T>C (p.Tyr2006His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39197 NM_198578.3(LRRK2):c.4872C>A (p.Gly1624=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2411 NM_032409.2(PINK1):c.836G>A (p.Arg279His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2409 NM_032409.2(PINK1):c.1570_1573dupTTAG (p.Asp525Valfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+dbSNP:rs34637584 rs34637584-A NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:39218 NM_198578.3(LRRK2):c.6035T>C (p.Ile2012Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+NCBIGene:170534 PARK10 NCBITaxon:9606 Homo sapiens RO:0002326 contributes to NCBIGene:170534 PARK10 ECO:0000177 genomic context evidence http://data.monarchinitiative.org/ttl/omim.ttl direct
+ClinVarVariant:7679 NR4A2, 1-BP DEL, -291T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7043 NM_004562.2(PARK2):c.483A>T (p.Lys161Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39227 NM_198578.3(LRRK2):c.6428G>A (p.Arg2143His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:88844 NM_203446.2(SYNJ1):c.773G>A (p.Arg258Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:615530 Parkinson Disease 20, Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7055 PARK2, EX5-6 DEL NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:1219 NM_022089.3(ATP13A2):c.1306+5G>A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7045 NM_004562.2(PARK2):c.735-?_871+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7042 NM_004562.2(PARK2):c.1358G>A (p.Trp453Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39226 NM_198578.3(LRRK2):c.6422C>T (p.Thr2141Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39139 NM_198578.3(LRRK2):c.1653C>G (p.Asn551Lys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96726 NM_007262.4(PARK7):c.399G>C (p.Met133Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4335 NM_001005741.2(GBA):c.1444G>A (p.Asp482Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7066 NM_007262.4(PARK7):c.446A>C (p.Asp149Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39180 NM_198578.3(LRRK2):c.4258G>A (p.Asp1420Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:6078 NM_005460.3(SNCAIP):c.1861C>T (p.Arg621Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7037 NM_004562.2(PARK2):c.931C>T (p.Gln311Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:189240 NM_032409.2(PINK1):c.620delG (p.Arg207Glnfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39200 NM_198578.3(LRRK2):c.4937T>C (p.Met1646Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7045 NM_004562.2(PARK2):c.735-?_871+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39229 NM_198578.3(LRRK2):c.6566A>G (p.Tyr2189Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39228 NM_198578.3(LRRK2):c.6510C>A (p.Gly2170=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:31151 NG_031977.1:g.5321_5326GGGGCC(24_?) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:7044 PARK2, 1-BP DEL, 202A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39136 NM_198578.3(LRRK2):c.155C>T (p.Ser52Phe) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39223 NM_198578.3(LRRK2):c.632C>T (p.Ala211Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7053 NM_004562.2(PARK2):c.7+1G>T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:16763 NM_001044.4(SLC6A3):c.1103T>A (p.Leu368Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613135 Parkinsonism-Dystonia, Infantile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39222 NM_198578.3(LRRK2):c.6324G>A (p.Glu2108=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39135 NM_198578.3(LRRK2):c.1517G>A (p.Arg506Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9705 m.12397A>G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7041 NM_004562.2(PARK2):c.872-?_1083+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41222 NM_004562.2(PARK2):c.1180G>A (p.Asp394Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1218 ATP13A2, 1-BP DEL, 3057C NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9705 m.12397A>G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39225 NM_198578.3(LRRK2):c.6415T>A (p.Cys2139Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39138 NM_198578.3(LRRK2):c.1630A>G (p.Lys544Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:88855 NM_001256865.1(DNAJC6):c.2200C>T (p.Gln734Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:615528 Parkinson Disease 19, Juvenile-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39137 NM_198578.3(LRRK2):c.1561A>G (p.Arg521Gly) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:88854 NM_001256864.1(DNAJC6):c.801-2A>G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:615528 Parkinson Disease 19, Juvenile-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7040 NM_004562.2(PARK2):c.8-?_171+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:16764 NM_001044.4(SLC6A3):c.1184C>T (p.Pro395Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613135 Parkinsonism-Dystonia, Infantile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39198 NM_198578.3(LRRK2):c.4883G>C (p.Arg1628Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7034 NM_004562.2(PARK2):c.172-?_871+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7680 NR4A2, -245T-G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39219 NM_198578.3(LRRK2):c.6091A>T (p.Thr2031Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7035 NM_004562.2(PARK2):c.413-?_534+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39199 NM_198578.3(LRRK2):c.4911A>G (p.Lys1637=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7055 PARK2, EX5-6 DEL NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:14009 SNCA, TRIPLICATION NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:39170 NM_198578.3(LRRK2):c.364C= (p.Leu122=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:12297 NM_004181.4(UCHL1):c.279C>G (p.Ile93Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39224 NM_198578.3(LRRK2):c.6356C>T (p.Pro2119Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:14011 SNCA, DUPLICATION NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168601 autosomal dominant Parkinson disease 1 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2407 NM_032409.2(PINK1):c.736C>T (p.Arg246Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39131 NM_198578.3(LRRK2):c.1256C>T (p.Ala419Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+dbSNP:rs34637584 rs34637584-A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2415 NM_032409.2(PINK1):c.1366C>T (p.Gln456Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7067 NM_007262.4(PARK7):c.192G>C (p.Glu64Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7040 NM_004562.2(PARK2):c.8-?_171+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7038 NM_004562.2(PARK2):c.245C>A (p.Ala82Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2406 NM_032409.2(PINK1):c.1311G>A (p.Trp437Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+dbSNP:rs6265 rs6265-C NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39130 NM_198578.3(LRRK2):c.1096G>A (p.Val366Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
diff -r 000000000000 -r 850bb90bd667 test-data/variants-for-diseases-intersection.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/variants-for-diseases-intersection.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,33 @@
+ClinVarVariant:8113 NM_002973.3(ATXN2):c.496_498CAG(15_24) (p.Gln188_Pro189insGlnGln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9726 m.3397A>G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:29936 NM_012084.3(GLUD2):c.1492T>G (p.Ser498Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4885 FGF20, 951C/T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:98243 NM_016835.4(MAPT):c.1838_1840delATA (p.Asn613del) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4295 NM_001005741.2(GBA):c.1504C>T (p.Arg502Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7040 NM_004562.2(PARK2):c.8-?_171+?del NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:56171 NM_015268.3(DNAJC13):c.2564A>G (p.Asn855Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:6144 NR_002717.2(ATXN8OS):n.1103_1105CTG(15_40) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7038 NM_004562.2(PARK2):c.245C>A (p.Ala82Glu) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:96731 NM_198578.3(LRRK2):c.7300A>G (p.Ile2434Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:3551 NM_004993.5(ATXN3):c.892_894CAG(8_36) (p.Gln298_Gln305=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96729 NM_032409.2(PINK1):c.923T>A (p.Leu308Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96730 NM_198578.3(LRRK2):c.2352C>A (p.Ser784Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7035 NM_004562.2(PARK2):c.413-?_534+?del NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:96728 NM_032409.2(PINK1):c.644C>T (p.Pro215Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:38301 NM_001005741.2(GBA):c.1226A>C (p.Asn409Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96727 NM_018206.4(VPS35):c.1576C>T (p.Arg526Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4288 NM_001005741.2(GBA):c.1448T>C (p.Leu483Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1936 NM_198578.3(LRRK2):c.4321C>G (p.Arg1441Gly) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:7050 NM_004562.2(PARK2):c.823C>T (p.Arg275Trp) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:9449 NM_003194.4(TBP):c.172_174CAG(25_42) (p.Gln95(25_42)) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7048 PARK2, 1-BP DEL, 255A NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+dbSNP:rs34637584 rs34637584-A NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:7679 NR4A2, 1-BP DEL, -291T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7055 PARK2, EX5-6 DEL NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:96726 NM_007262.4(PARK7):c.399G>C (p.Met133Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4335 NM_001005741.2(GBA):c.1444G>A (p.Asp482Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:6078 NM_005460.3(SNCAIP):c.1861C>T (p.Arg621Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:31151 NG_031977.1:g.5321_5326GGGGCC(24_?) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:7680 NR4A2, -245T-G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:14009 SNCA, TRIPLICATION NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+dbSNP:rs6265 rs6265-C NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
diff -r 000000000000 -r 850bb90bd667 test-data/variants-for-diseases-union.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/variants-for-diseases-union.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,316 @@
+ClinVarVariant:39148 NM_198578.3(LRRK2):c.2264C>T (p.Pro755Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7051 NM_004562.2(PARK2):c.633A>T (p.Lys211Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1936 NM_198578.3(LRRK2):c.4321C>G (p.Arg1441Gly) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4810 NM_012179.3(FBXO7):c.1144+1G>T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:260300 autosomal recessive early-onset Parkinson disease 15 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39147 NM_198578.3(LRRK2):c.225G>A (p.Ala75=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39234 NM_198578.3(LRRK2):c.7155A>G (p.Gly2385=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2412 NM_005216.4(DDOST):c.*807_*5409del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7050 NM_004562.2(PARK2):c.823C>T (p.Arg275Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9695 m.14319T>C NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39128 NM_198578.3(LRRK2):c.1000G>A (p.Glu334Lys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39215 NM_198578.3(LRRK2):c.5620G>T (p.Glu1874Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39195 NM_198578.3(LRRK2):c.4793T>A (p.Val1598Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:209135 NM_022089.3(ATP13A2):c.348-9_351del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4809 NM_012179.3(FBXO7):c.1492C>T (p.Arg498Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:260300 autosomal recessive early-onset Parkinson disease 15 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39214 NM_198578.3(LRRK2):c.5610G>T (p.Leu1870Phe) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:143196 NM_022089.3(ATP13A2):c.490C>T (p.Arg164Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39194 NM_198578.3(LRRK2):c.4666C>A (p.Leu1556Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7042 NM_004562.2(PARK2):c.1358G>A (p.Trp453Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9695 m.14319T>C NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39213 NM_198578.3(LRRK2):c.5606T>C (p.Met1869Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39193 NM_198578.3(LRRK2):c.4624C>T (p.Pro1542Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+NCBIGene:677662 PARK12 NCBITaxon:9606 Homo sapiens RO:0002326 contributes to NCBIGene:677662 PARK12 ECO:0000177 genomic context evidence http://data.monarchinitiative.org/ttl/omim.ttl direct
+ClinVarVariant:39192 NM_198578.3(LRRK2):c.457T>C (p.Leu153=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39212 NM_198578.3(LRRK2):c.5605A>G (p.Met1869Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+NCBIGene:5072 PARK3 NCBITaxon:9606 Homo sapiens RO:0002326 contributes to NCBIGene:5072 PARK3 ECO:0000177 genomic context evidence http://data.monarchinitiative.org/ttl/omim.ttl direct
+ClinVarVariant:4808 NM_012179.3(FBXO7):c.1132C>G (p.Arg378Gly) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:260300 autosomal recessive early-onset Parkinson disease 15 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39191 NM_198578.3(LRRK2):c.4541G>A (p.Arg1514Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30371 NM_003560.2(PLA2G6):c.991G>T (p.Asp331Tyr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:612953 Parkinson Disease 14, Autosomal Recessive http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39238 NM_198578.3(LRRK2):c.7190T= (p.Met2397=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7053 NM_004562.2(PARK2):c.7+1G>T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:50354 NM_004562.2(PARK2):c.1292G>T (p.Cys431Phe) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2404 NM_032409.2(PINK1):c.926G>A (p.Gly309Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39237 NM_198578.3(LRRK2):c.7186_7187dupGT (p.Met2397Terfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1937 NM_198578.3(LRRK2):c.5096A>G (p.Tyr1699Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4811 NM_012179.3(FBXO7):c.65C>T (p.Thr22Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:260300 autosomal recessive early-onset Parkinson disease 15 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7052 PARK2, 1-BP DEL, 1072T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39149 NM_198578.3(LRRK2):c.2378G>T (p.Arg793Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39236 NM_198578.3(LRRK2):c.7183G>A (p.Glu2395Lys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:8113 NM_002973.3(ATXN2):c.496_498CAG(15_24) (p.Gln188_Pro189insGlnGln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39235 NM_198578.3(LRRK2):c.7168G>A (p.Val2390Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:12298 NM_004181.4(UCHL1):c.53C>A (p.Ser18Tyr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613643 Parkinson Disease 5, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39211 NM_198578.3(LRRK2):c.546A>G (p.Lys182=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7048 PARK2, 1-BP DEL, 255A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4342 NM_013247.4(HTRA2):c.421G>T (p.Ala141Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:12297 NM_004181.4(UCHL1):c.279C>G (p.Ile93Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613643 Parkinson Disease 5, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7050 NM_004562.2(PARK2):c.823C>T (p.Arg275Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9726 m.3397A>G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7055 PARK2, EX5-6 DEL NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39210 NM_198578.3(LRRK2):c.5467C>A (p.Gln1823Lys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39190 NM_198578.3(LRRK2):c.4448G>A (p.Arg1483Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39239 NM_198578.3(LRRK2):c.7224G>A (p.Met2408Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:29936 NM_012084.3(GLUD2):c.1492T>G (p.Ser498Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4885 FGF20, 951C/T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1939 NM_198578.3(LRRK2):c.3364A>G (p.Ile1122Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39233 NM_198578.3(LRRK2):c.713A>T (p.Asn238Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39146 NM_198578.3(LRRK2):c.2167A>G (p.Ile723Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7035 NM_004562.2(PARK2):c.413-?_534+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:98243 NM_016835.4(MAPT):c.1838_1840delATA (p.Asn613del) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9579 m.8344A>G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7064 NM_007262.4(PARK7):c.497T>C (p.Leu166Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39232 NM_198578.3(LRRK2):c.7067C>T (p.Thr2356Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39145 NM_198578.3(LRRK2):c.2147C>T (p.Ala716Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4295 NM_001005741.2(GBA):c.1504C>T (p.Arg502Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:18181 NM_000669.4(ADH1C):c.232G>T (p.Gly78Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39231 NM_198578.3(LRRK2):c.683G>C (p.Cys228Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39144 NM_198578.3(LRRK2):c.2134A>G (p.Met712Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7040 NM_004562.2(PARK2):c.8-?_171+?del NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:39143 NM_198578.3(LRRK2):c.2022A>C (p.Val674=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7043 NM_004562.2(PARK2):c.483A>T (p.Lys161Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39230 NM_198578.3(LRRK2):c.6782A>T (p.Asn2261Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:6204 NM_003560.2(PLA2G6):c.2239C>T (p.Arg747Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:612953 Parkinson Disease 14, Autosomal Recessive http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2409 NM_032409.2(PINK1):c.1570_1573dupTTAG (p.Asp525Valfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39221 NM_198578.3(LRRK2):c.6241A>G (p.Asn2081Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2407 NM_032409.2(PINK1):c.736C>T (p.Arg246Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39134 NM_198578.3(LRRK2):c.149A>G (p.His50Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:6203 NM_003560.2(PLA2G6):c.2222G>A (p.Arg741Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:612953 Parkinson Disease 14, Autosomal Recessive http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30583 NM_013247.4(HTRA2):c.427C>G (p.Pro143Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39132 NM_198578.3(LRRK2):c.1383T= (p.Ser461=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2408 NM_032409.2(PINK1):c.1040T>C (p.Leu347Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39220 NM_198578.3(LRRK2):c.6187_6191delCTCTA (p.Leu2063Terfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39133 NM_198578.3(LRRK2):c.1464A>T (p.Leu488=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:56171 NM_015268.3(DNAJC13):c.2564A>G (p.Asn855Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39243 NM_198578.3(LRRK2):c.825T= (p.His275=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:755 NM_015575.3(GIGYF2):c.1818C>G (p.Asp606Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39156 NM_198578.3(LRRK2):c.2857T>C (p.Leu953=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:14009 SNCA, TRIPLICATION NCBITaxon:9606 Homo sapiens OMIM:168601 autosomal dominant Parkinson disease 1 http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:7046 NM_004562.2(PARK2):c.635G>A (p.Cys212Tyr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:6144 NR_002717.2(ATXN8OS):n.1103_1105CTG(15_40) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+NCBIGene:100359403 PARK16 NCBITaxon:9606 Homo sapiens RO:0002326 contributes to NCBIGene:100359403 PARK16 ECO:0000177 genomic context evidence http://data.monarchinitiative.org/ttl/omim.ttl direct
+ClinVarVariant:1942 NM_198578.3(LRRK2):c.4322G>A (p.Arg1441His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:29685 NM_001044.4(SLC6A3):c.1269+1G>A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613135 Parkinsonism-Dystonia, Infantile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9054 NM_021074.4(NDUFV2):c.86T>C (p.Val29Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39155 NM_198578.3(LRRK2):c.2830G>T (p.Asp944Tyr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:754 NM_015575.3(GIGYF2):c.1370A>C (p.Asn457Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39242 NM_198578.3(LRRK2):c.7468delC (p.Gln2490Asnfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41223 NM_004562.2(PARK2):c.500G>A (p.Ser167Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:757 NM_015575.3(GIGYF2):c.1262A>G (p.Lys421Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39158 NM_198578.3(LRRK2):c.2918G>A (p.Ser973Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41222 NM_004562.2(PARK2):c.1180G>A (p.Asp394Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:66098 NM_022089.3(ATP13A2):c.2561T>G (p.Met854Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39167 NM_198578.3(LRRK2):c.356T>C (p.Leu119Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2405 NM_032409.2(PINK1):c.813C>A (p.His271Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2414 NM_032409.2(PINK1):c.650C>A (p.Ala217Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41223 NM_004562.2(PARK2):c.500G>A (p.Ser167Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39169 NM_198578.3(LRRK2):c.3647A>G (p.His1216Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7038 NM_004562.2(PARK2):c.245C>A (p.Ala82Glu) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:97017 NM_001044.4(SLC6A3):c.671T>C (p.Leu224Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613135 Parkinsonism-Dystonia, Infantile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:97000 NM_000345.3(SNCA):c.152G>A (p.Gly51Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168601 autosomal dominant Parkinson disease 1 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2415 NM_032409.2(PINK1):c.1366C>T (p.Gln456Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2412 NM_005216.4(DDOST):c.*807_*5409del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:60700 NM_007262.4(PARK7):c.-24+75_-24+92dup NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39165 NM_198578.3(LRRK2):c.3451G>A (p.Ala1151Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96731 NM_198578.3(LRRK2):c.7300A>G (p.Ile2434Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:216934 NM_001103146.1(GIGYF2):c.2378C>T (p.Ala793Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2413 NM_032409.2(PINK1):c.938C>T (p.Thr313Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41221 NM_004562.2(PARK2):c.1138G>C (p.Val380Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39166 NM_198578.3(LRRK2):c.3494T>C (p.Leu1165Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41220 NM_004562.2(PARK2):c.1096C>T (p.Arg366Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4342 NM_013247.4(HTRA2):c.421G>T (p.Ala141Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2410 PINK1, 3-BP INS, 1602CAA NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7065 NM_007262.4(PARK7):c.78G>A (p.Met26Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7036 NM_004562.2(PARK2):c.719C>G (p.Thr240Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39163 NM_198578.3(LRRK2):c.3333G>T (p.Gln1111His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2405 NM_032409.2(PINK1):c.813C>A (p.His271Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39246 NM_198578.3(LRRK2):c.936G>T (p.Ala312=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:14009 SNCA, TRIPLICATION NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605543 Parkinson Disease 4, Autosomal Dominant http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39159 NM_198578.3(LRRK2):c.3018A>G (p.Ile1006Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39244 NM_198578.3(LRRK2):c.867C= (p.Asn289=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:756 NM_015575.3(GIGYF2):c.832A>G (p.Ile278Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39157 NM_198578.3(LRRK2):c.28G>A (p.Glu10Lys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2404 NM_032409.2(PINK1):c.926G>A (p.Gly309Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39245 NM_198578.3(LRRK2):c.894T>C (p.Ala298=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:97016 NM_001044.4(SLC6A3):c.1031+1G>A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613135 Parkinsonism-Dystonia, Infantile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:3551 NM_004993.5(ATXN3):c.892_894CAG(8_36) (p.Gln298_Gln305=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39168 NM_198578.3(LRRK2):c.3574A>G (p.Ile1192Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:66099 NM_022089.3(ATP13A2):c.2629G>A (p.Gly877Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4341 NM_013247.4(HTRA2):c.1195G>A (p.Gly399Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9571 m.15965A>G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2411 NM_032409.2(PINK1):c.836G>A (p.Arg279His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2413 NM_032409.2(PINK1):c.938C>T (p.Thr313Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39164 NM_198578.3(LRRK2):c.3342A>G (p.Leu1114=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96729 NM_032409.2(PINK1):c.923T>A (p.Leu308Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39161 NM_198578.3(LRRK2):c.3200G>A (p.Arg1067Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39189 NM_198578.3(LRRK2):c.4402A>G (p.Lys1468Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39209 NM_198578.3(LRRK2):c.5457T>C (p.Gly1819=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39160 NM_198578.3(LRRK2):c.3021T= (p.Ser1007=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9559 m.15950G>A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:556500 Parkinson Disease, Mitochondrial http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7044 PARK2, 1-BP DEL, 202A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39206 NM_198578.3(LRRK2):c.5183G>A (p.Arg1728His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30368 PLA2G6, PHE72LEU NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:612953 Parkinson Disease 14, Autosomal Recessive http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39186 NM_198578.3(LRRK2):c.4337C>T (p.Pro1446Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7052 PARK2, 1-BP DEL, 1072T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39162 NM_198578.3(LRRK2):c.3287C>G (p.Ser1096Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96730 NM_198578.3(LRRK2):c.2352C>A (p.Ser784Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39278 NM_198578.3(LRRK2):c.6523G>C (p.Asp2175His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7035 NM_004562.2(PARK2):c.413-?_534+?del NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:39208 NM_198578.3(LRRK2):c.5385G>T (p.Leu1795Phe) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30583 NM_013247.4(HTRA2):c.427C>G (p.Pro143Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:610297 Parkinson Disease 13, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39188 NM_198578.3(LRRK2):c.4364_4365delAT (p.Asp1455Glyfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41221 NM_004562.2(PARK2):c.1138G>C (p.Val380Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39187 NM_198578.3(LRRK2):c.4348G>A (p.Val1450Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96728 NM_032409.2(PINK1):c.644C>T (p.Pro215Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:38301 NM_001005741.2(GBA):c.1226A>C (p.Asn409Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39183 NM_198578.3(LRRK2):c.4309A>C (p.Asn1437His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2406 NM_032409.2(PINK1):c.1311G>A (p.Trp437Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39184 NM_198578.3(LRRK2):c.4323C>T (p.Arg1441=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30366 NM_003560.2(PLA2G6):c.1904G>A (p.Arg635Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:612953 Parkinson Disease 14, Autosomal Recessive http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39204 NM_198578.3(LRRK2):c.5173C>T (p.Arg1725Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96727 NM_018206.4(VPS35):c.1576C>T (p.Arg526Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39185 NM_198578.3(LRRK2):c.4324G>C (p.Ala1442Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30367 NM_003560.2(PLA2G6):c.1354C>T (p.Gln452Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:612953 Parkinson Disease 14, Autosomal Recessive http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39205 NM_198578.3(LRRK2):c.5174G>A (p.Arg1725Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39181 NM_198578.3(LRRK2):c.4269G>A (p.Lys1423=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7046 NM_004562.2(PARK2):c.635G>A (p.Cys212Tyr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2414 NM_032409.2(PINK1):c.650C>A (p.Ala217Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39201 NM_198578.3(LRRK2):c.4939T>A (p.Ser1647Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:189240 NM_032409.2(PINK1):c.620delG (p.Arg207Glnfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7047 NM_004562.2(PARK2):c.167T>A (p.Val56Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:183259 NM_032409.2(PINK1):c.799C>T (p.Gln267Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39202 NM_198578.3(LRRK2):c.4959A>G (p.Leu1653=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39182 NM_198578.3(LRRK2):c.4290C>T (p.Ala1430=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4288 NM_001005741.2(GBA):c.1448T>C (p.Leu483Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7048 PARK2, 1-BP DEL, 255A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39203 NM_198578.3(LRRK2):c.5163A>G (p.Ser1721=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39151 NM_198578.3(LRRK2):c.2481T>C (p.Ser827=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+dbSNP:rs34778348 rs34778348-? NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2408 NM_032409.2(PINK1):c.1040T>C (p.Leu347Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2410 PINK1, 3-BP INS, 1602CAA NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1936 NM_198578.3(LRRK2):c.4321C>G (p.Arg1441Gly) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:39152 NM_198578.3(LRRK2):c.2611A>G (p.Lys871Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30833 NM_022089.3(ATP13A2):c.1101_1102dupGA (p.Thr368Argfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:14008 NM_000345.3(SNCA):c.88G>C (p.Ala30Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168601 autosomal dominant Parkinson disease 1 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39240 NM_198578.3(LRRK2):c.7397T>A (p.Leu2466His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41220 NM_004562.2(PARK2):c.1096C>T (p.Arg366Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39142 NM_198578.3(LRRK2):c.1987T>C (p.Ser663Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1221 NM_022089.3(ATP13A2):c.1510G>C (p.Gly504Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7051 NM_004562.2(PARK2):c.633A>T (p.Lys211Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:97018 NM_001044.4(SLC6A3):c.1561C>T (p.Arg521Trp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613135 Parkinsonism-Dystonia, Infantile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39140 NM_198578.3(LRRK2):c.1674G= (p.Gly558=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39141 NM_198578.3(LRRK2):c.1847A>G (p.Lys616Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:60700 NM_007262.4(PARK7):c.-24+75_-24+92dup NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1220 ATP13A2, 22-BP DUP NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39153 NM_198578.3(LRRK2):c.2769G>C (p.Gln923His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30834 NM_022089.3(ATP13A2):c.2552_2553delTT (p.Phe851Cysfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7050 NM_004562.2(PARK2):c.823C>T (p.Arg275Trp) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:39154 NM_198578.3(LRRK2):c.2789A>G (p.Gln930Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:753 NM_015575.3(GIGYF2):c.167A>G (p.Asn56Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607688 Parkinson Disease 11, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39241 NM_198578.3(LRRK2):c.7435A>G (p.Asn2479Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1941 NM_198578.3(LRRK2):c.6059T>C (p.Ile2020Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:12298 NM_004181.4(UCHL1):c.53C>A (p.Ser18Tyr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7064 NM_007262.4(PARK7):c.497T>C (p.Leu166Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39176 NM_198578.3(LRRK2):c.4111A>G (p.Ile1371Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39175 NM_198578.3(LRRK2):c.3974G>A (p.Arg1325Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7065 NM_007262.4(PARK7):c.78G>A (p.Met26Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39177 NM_198578.3(LRRK2):c.4125C>A (p.Asp1375Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30072 NM_198241.2(EIF4G1):c.3614G>A (p.Arg1205His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:56171 NM_015268.3(DNAJC13):c.2564A>G (p.Asn855Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:616361 Parkinson Disease 21 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:162095 NM_000345.3(SNCA):c.150T>G (p.His50Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168601 autosomal dominant Parkinson disease 1 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7041 NM_004562.2(PARK2):c.872-?_1083+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9449 NM_003194.4(TBP):c.172_174CAG(25_42) (p.Gln95(25_42)) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30073 NM_198241.2(EIF4G1):c.1505C>T (p.Ala502Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:614251 Parkinson Disease 18, Autosomal Dominant, Susceptibility to http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39178 NM_198578.3(LRRK2):c.4193G>A (p.Arg1398His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7048 PARK2, 1-BP DEL, 255A NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:7066 NM_007262.4(PARK7):c.446A>C (p.Asp149Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:14007 NM_000345.3(SNCA):c.157G>A (p.Ala53Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168601 autosomal dominant Parkinson disease 1 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39179 NM_198578.3(LRRK2):c.4229C>T (p.Thr1410Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39150 NM_198578.3(LRRK2):c.2428A>G (p.Ile810Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7067 NM_007262.4(PARK7):c.192G>C (p.Glu64Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39171 NM_198578.3(LRRK2):c.3683G>C (p.Ser1228Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7036 NM_004562.2(PARK2):c.719C>G (p.Thr240Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7037 NM_004562.2(PARK2):c.931C>T (p.Gln311Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7038 NM_004562.2(PARK2):c.245C>A (p.Ala82Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7047 NM_004562.2(PARK2):c.167T>A (p.Val56Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39173 NM_198578.3(LRRK2):c.3784C>G (p.Pro1262Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4341 NM_013247.4(HTRA2):c.1195G>A (p.Gly399Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:30196 NM_018206.4(VPS35):c.1858G>A (p.Asp620Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:614203 Parkinson Disease 17 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:183259 NM_032409.2(PINK1):c.799C>T (p.Gln267Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39174 NM_198578.3(LRRK2):c.3960G>T (p.Arg1320Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7063 NC_000001.10:g.(8018845_8022846)_(8037799_8044954)del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606324 Parkinson Disease 7, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:209136 NM_022089.3(ATP13A2):c.943G>A (p.Gly315Arg) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39216 NM_198578.3(LRRK2):c.5822G>A (p.Arg1941His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39196 NM_198578.3(LRRK2):c.4838T>C (p.Val1613Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39129 NM_198578.3(LRRK2):c.1088A>G (p.Asn363Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7034 NM_004562.2(PARK2):c.172-?_871+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:50354 NM_004562.2(PARK2):c.1292G>T (p.Cys431Phe) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7063 NC_000001.10:g.(8018845_8022846)_(8037799_8044954)del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39217 NM_198578.3(LRRK2):c.6016T>C (p.Tyr2006His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39197 NM_198578.3(LRRK2):c.4872C>A (p.Gly1624=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2411 NM_032409.2(PINK1):c.836G>A (p.Arg279His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2409 NM_032409.2(PINK1):c.1570_1573dupTTAG (p.Asp525Valfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+dbSNP:rs34637584 rs34637584-A NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:39218 NM_198578.3(LRRK2):c.6035T>C (p.Ile2012Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+NCBIGene:170534 PARK10 NCBITaxon:9606 Homo sapiens RO:0002326 contributes to NCBIGene:170534 PARK10 ECO:0000177 genomic context evidence http://data.monarchinitiative.org/ttl/omim.ttl direct
+ClinVarVariant:7679 NR4A2, 1-BP DEL, -291T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7043 NM_004562.2(PARK2):c.483A>T (p.Lys161Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39227 NM_198578.3(LRRK2):c.6428G>A (p.Arg2143His) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:88844 NM_203446.2(SYNJ1):c.773G>A (p.Arg258Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:615530 Parkinson Disease 20, Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7055 PARK2, EX5-6 DEL NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:1219 NM_022089.3(ATP13A2):c.1306+5G>A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7045 NM_004562.2(PARK2):c.735-?_871+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7042 NM_004562.2(PARK2):c.1358G>A (p.Trp453Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39226 NM_198578.3(LRRK2):c.6422C>T (p.Thr2141Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39139 NM_198578.3(LRRK2):c.1653C>G (p.Asn551Lys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:96726 NM_007262.4(PARK7):c.399G>C (p.Met133Ile) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:4335 NM_001005741.2(GBA):c.1444G>A (p.Asp482Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7066 NM_007262.4(PARK7):c.446A>C (p.Asp149Ala) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39180 NM_198578.3(LRRK2):c.4258G>A (p.Asp1420Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:6078 NM_005460.3(SNCAIP):c.1861C>T (p.Arg621Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7037 NM_004562.2(PARK2):c.931C>T (p.Gln311Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:189240 NM_032409.2(PINK1):c.620delG (p.Arg207Glnfs) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39200 NM_198578.3(LRRK2):c.4937T>C (p.Met1646Thr) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7045 NM_004562.2(PARK2):c.735-?_871+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39229 NM_198578.3(LRRK2):c.6566A>G (p.Tyr2189Cys) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39228 NM_198578.3(LRRK2):c.6510C>A (p.Gly2170=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:31151 NG_031977.1:g.5321_5326GGGGCC(24_?) NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:7044 PARK2, 1-BP DEL, 202A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39136 NM_198578.3(LRRK2):c.155C>T (p.Ser52Phe) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39223 NM_198578.3(LRRK2):c.632C>T (p.Ala211Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7053 NM_004562.2(PARK2):c.7+1G>T NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:16763 NM_001044.4(SLC6A3):c.1103T>A (p.Leu368Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613135 Parkinsonism-Dystonia, Infantile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39222 NM_198578.3(LRRK2):c.6324G>A (p.Glu2108=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39135 NM_198578.3(LRRK2):c.1517G>A (p.Arg506Gln) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9705 m.12397A>G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7041 NM_004562.2(PARK2):c.872-?_1083+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:41222 NM_004562.2(PARK2):c.1180G>A (p.Asp394Asn) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:1218 ATP13A2, 1-BP DEL, 3057C NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:606693 Kufor-Rakeb syndrome http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:9705 m.12397A>G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39225 NM_198578.3(LRRK2):c.6415T>A (p.Cys2139Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39138 NM_198578.3(LRRK2):c.1630A>G (p.Lys544Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:88855 NM_001256865.1(DNAJC6):c.2200C>T (p.Gln734Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:615528 Parkinson Disease 19, Juvenile-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39137 NM_198578.3(LRRK2):c.1561A>G (p.Arg521Gly) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:88854 NM_001256864.1(DNAJC6):c.801-2A>G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:615528 Parkinson Disease 19, Juvenile-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7040 NM_004562.2(PARK2):c.8-?_171+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:16764 NM_001044.4(SLC6A3):c.1184C>T (p.Pro395Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:613135 Parkinsonism-Dystonia, Infantile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39198 NM_198578.3(LRRK2):c.4883G>C (p.Arg1628Pro) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7034 NM_004562.2(PARK2):c.172-?_871+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7680 NR4A2, -245T-G NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39219 NM_198578.3(LRRK2):c.6091A>T (p.Thr2031Ser) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7035 NM_004562.2(PARK2):c.413-?_534+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:600116 Parkinson Disease 2, Autosomal Recessive Juvenile http://data.monarchinitiative.org/ttl/coriell.ttl|http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39199 NM_198578.3(LRRK2):c.4911A>G (p.Lys1637=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7055 PARK2, EX5-6 DEL NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:14009 SNCA, TRIPLICATION NCBITaxon:9606 Homo sapiens OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/coriell.ttl inferred
+ClinVarVariant:39170 NM_198578.3(LRRK2):c.364C= (p.Leu122=) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:12297 NM_004181.4(UCHL1):c.279C>G (p.Ile93Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39224 NM_198578.3(LRRK2):c.6356C>T (p.Pro2119Leu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:14011 SNCA, DUPLICATION NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168601 autosomal dominant Parkinson disease 1 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2407 NM_032409.2(PINK1):c.736C>T (p.Arg246Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39131 NM_198578.3(LRRK2):c.1256C>T (p.Ala419Val) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+dbSNP:rs34637584 rs34637584-A NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2415 NM_032409.2(PINK1):c.1366C>T (p.Gln456Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7067 NM_007262.4(PARK7):c.192G>C (p.Glu64Asp) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7040 NM_004562.2(PARK2):c.8-?_171+?del NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:7038 NM_004562.2(PARK2):c.245C>A (p.Ala82Glu) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype Orphanet:2828 Young-onset Parkinson disease http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:2406 NM_032409.2(PINK1):c.1311G>A (p.Trp437Ter) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:605909 Parkinson Disease 6, Autosomal Recessive Early-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+dbSNP:rs6265 rs6265-C NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:168600 Parkinson Disease, Late-Onset http://data.monarchinitiative.org/ttl/clinvar.ttl direct
+ClinVarVariant:39130 NM_198578.3(LRRK2):c.1096G>A (p.Val366Met) NCBITaxon:9606 Homo sapiens RO:0002200 has phenotype OMIM:607060 autosomal dominant Parkinson disease 8 http://data.monarchinitiative.org/ttl/clinvar.ttl direct
diff -r 000000000000 -r 850bb90bd667 test-data/variants-for-phenotype.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/variants-for-phenotype.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,184 @@
+ClinVarVariant:13509 NM_002693.2(POLG):c.2492A>G (p.Tyr831Cys) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39216 NM_198578.3(LRRK2):c.5822G>A (p.Arg1941His) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39156 NM_198578.3(LRRK2):c.2857T>C (p.Leu953=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39146 NM_198578.3(LRRK2):c.2167A>G (p.Ile723Val) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39136 NM_198578.3(LRRK2):c.155C>T (p.Ser52Phe) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39206 NM_198578.3(LRRK2):c.5183G>A (p.Arg1728His) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39246 NM_198578.3(LRRK2):c.936G>T (p.Ala312=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39236 NM_198578.3(LRRK2):c.7183G>A (p.Glu2395Lys) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39226 NM_198578.3(LRRK2):c.6422C>T (p.Thr2141Met) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39176 NM_198578.3(LRRK2):c.4111A>G (p.Ile1371Val) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39166 NM_198578.3(LRRK2):c.3494T>C (p.Leu1165Pro) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39186 NM_198578.3(LRRK2):c.4337C>T (p.Pro1446Leu) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39196 NM_198578.3(LRRK2):c.4838T>C (p.Val1613Ala) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:209135 NM_022089.3(ATP13A2):c.348-9_351del NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:755 NM_015575.3(GIGYF2):c.1818C>G (p.Asp606Glu) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39191 NM_198578.3(LRRK2):c.4541G>A (p.Arg1514Gln) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39181 NM_198578.3(LRRK2):c.4269G>A (p.Lys1423=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39171 NM_198578.3(LRRK2):c.3683G>C (p.Ser1228Thr) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39161 NM_198578.3(LRRK2):c.3200G>A (p.Arg1067Gln) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39151 NM_198578.3(LRRK2):c.2481T>C (p.Ser827=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39141 NM_198578.3(LRRK2):c.1847A>G (p.Lys616Arg) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39131 NM_198578.3(LRRK2):c.1256C>T (p.Ala419Val) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:4808 NM_012179.3(FBXO7):c.1132C>G (p.Arg378Gly) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:12332 TH, 1-BP DEL, 291C NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:30833 NM_022089.3(ATP13A2):c.1101_1102dupGA (p.Thr368Argfs) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:12329 NM_199292.2(TH):c.826A>C (p.Thr276Pro) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9284 NM_000161.2(GCH1):c.586G>T (p.Ala196Ser) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9274 NM_000161.2(GCH1):c.602G>A (p.Gly201Glu) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:1218 ATP13A2, 1-BP DEL, 3057C NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:12327 NM_199292.2(TH):c.698G>A (p.Arg233His) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:4341 NM_013247.4(HTRA2):c.1195G>A (p.Gly399Ser) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:4811 NM_012179.3(FBXO7):c.65C>T (p.Thr22Met) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9289 GCH1, IVS5, G-A, +1 NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9279 GCH1, IVS2, G-C, +1 NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:188890 NM_000360.3(TH):c.1282C>T (p.Gln428Ter) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:753 NM_015575.3(GIGYF2):c.167A>G (p.Asn56Ser) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:1221 NM_022089.3(ATP13A2):c.1510G>C (p.Gly504Arg) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:1941 NM_198578.3(LRRK2):c.6059T>C (p.Ile2020Thr) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:30583 NM_013247.4(HTRA2):c.427C>G (p.Pro143Ala) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39214 NM_198578.3(LRRK2):c.5610G>T (p.Leu1870Phe) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39224 NM_198578.3(LRRK2):c.6356C>T (p.Pro2119Leu) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39204 NM_198578.3(LRRK2):c.5173C>T (p.Arg1725Ter) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39174 NM_198578.3(LRRK2):c.3960G>T (p.Arg1320Ser) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39184 NM_198578.3(LRRK2):c.4323C>T (p.Arg1441=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39194 NM_198578.3(LRRK2):c.4666C>A (p.Leu1556Ile) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39144 NM_198578.3(LRRK2):c.2134A>G (p.Met712Val) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39154 NM_198578.3(LRRK2):c.2789A>G (p.Gln930Arg) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39164 NM_198578.3(LRRK2):c.3342A>G (p.Leu1114=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39134 NM_198578.3(LRRK2):c.149A>G (p.His50Arg) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39199 NM_198578.3(LRRK2):c.4911A>G (p.Lys1637=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39189 NM_198578.3(LRRK2):c.4402A>G (p.Lys1468Glu) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39179 NM_198578.3(LRRK2):c.4229C>T (p.Thr1410Met) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39169 NM_198578.3(LRRK2):c.3647A>G (p.His1216Arg) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39159 NM_198578.3(LRRK2):c.3018A>G (p.Ile1006Met) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39149 NM_198578.3(LRRK2):c.2378G>T (p.Arg793Met) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39139 NM_198578.3(LRRK2):c.1653C>G (p.Asn551Lys) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39129 NM_198578.3(LRRK2):c.1088A>G (p.Asn363Ser) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:1936 NM_198578.3(LRRK2):c.4321C>G (p.Arg1441Gly) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39244 NM_198578.3(LRRK2):c.867C= (p.Asn289=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39234 NM_198578.3(LRRK2):c.7155A>G (p.Gly2385=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:66098 NM_022089.3(ATP13A2):c.2561T>G (p.Met854Arg) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:12325 NM_199292.2(TH):c.707T>C (p.Leu236Pro) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9277 NM_000161.2(GCH1):c.3G>C (p.Met1Ile) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9862 TAF1, SVA RETROTRANSPOSON INSERTION NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9272 NM_000161.2(GCH1):c.401A>T (p.Asp134Val) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39242 NM_198578.3(LRRK2):c.7468delC (p.Gln2490Asnfs) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39212 NM_198578.3(LRRK2):c.5605A>G (p.Met1869Val) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39222 NM_198578.3(LRRK2):c.6324G>A (p.Glu2108=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39232 NM_198578.3(LRRK2):c.7067C>T (p.Thr2356Ile) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39202 NM_198578.3(LRRK2):c.4959A>G (p.Leu1653=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39142 NM_198578.3(LRRK2):c.1987T>C (p.Ser663Pro) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39132 NM_198578.3(LRRK2):c.1383T= (p.Ser461=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39152 NM_198578.3(LRRK2):c.2611A>G (p.Lys871Glu) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39162 NM_198578.3(LRRK2):c.3287C>G (p.Ser1096Cys) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39182 NM_198578.3(LRRK2):c.4290C>T (p.Ala1430=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39192 NM_198578.3(LRRK2):c.457T>C (p.Leu153=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:4809 NM_012179.3(FBXO7):c.1492C>T (p.Arg498Ter) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:12330 NM_199292.2(TH):c.941C>T (p.Thr314Met) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39209 NM_198578.3(LRRK2):c.5457T>C (p.Gly1819=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39219 NM_198578.3(LRRK2):c.6091A>T (p.Thr2031Ser) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39229 NM_198578.3(LRRK2):c.6566A>G (p.Tyr2189Cys) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39239 NM_198578.3(LRRK2):c.7224G>A (p.Met2408Ile) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:13495 NM_002693.2(POLG):c.2864A>G (p.Tyr955Cys) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:209136 NM_022089.3(ATP13A2):c.943G>A (p.Gly315Arg) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:756 NM_015575.3(GIGYF2):c.832A>G (p.Ile278Val) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39137 NM_198578.3(LRRK2):c.1561A>G (p.Arg521Gly) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39177 NM_198578.3(LRRK2):c.4125C>A (p.Asp1375Glu) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39187 NM_198578.3(LRRK2):c.4348G>A (p.Val1450Ile) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39197 NM_198578.3(LRRK2):c.4872C>A (p.Gly1624=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39147 NM_198578.3(LRRK2):c.225G>A (p.Ala75=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39157 NM_198578.3(LRRK2):c.28G>A (p.Glu10Lys) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39167 NM_198578.3(LRRK2):c.356T>C (p.Leu119Pro) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39237 NM_198578.3(LRRK2):c.7186_7187dupGT (p.Met2397Terfs) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:4342 NM_013247.4(HTRA2):c.421G>T (p.Ala141Ser) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39227 NM_198578.3(LRRK2):c.6428G>A (p.Arg2143His) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39217 NM_198578.3(LRRK2):c.6016T>C (p.Tyr2006His) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:1219 NM_022089.3(ATP13A2):c.1306+5G>A NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:216934 NM_001103146.1(GIGYF2):c.2378C>T (p.Ala793Val) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9275 GCH1, IVS1, A-G, -2 NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9285 NM_000161.2(GCH1):c.404T>A (p.Ile135Lys) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:4810 NM_012179.3(FBXO7):c.1144+1G>T NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:1937 NM_198578.3(LRRK2):c.5096A>G (p.Tyr1699Cys) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:21011 NR_104387.1(TAF1):n.5894C>T NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:1939 NM_198578.3(LRRK2):c.3364A>G (p.Ile1122Val) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39140 NM_198578.3(LRRK2):c.1674G= (p.Gly558=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39130 NM_198578.3(LRRK2):c.1096G>A (p.Val366Met) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39150 NM_198578.3(LRRK2):c.2428A>G (p.Ile810Val) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39200 NM_198578.3(LRRK2):c.4937T>C (p.Met1646Thr) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39210 NM_198578.3(LRRK2):c.5467C>A (p.Gln1823Lys) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39230 NM_198578.3(LRRK2):c.6782A>T (p.Asn2261Ile) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39240 NM_198578.3(LRRK2):c.7397T>A (p.Leu2466His) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39220 NM_198578.3(LRRK2):c.6187_6191delCTCTA (p.Leu2063Terfs) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39160 NM_198578.3(LRRK2):c.3021T= (p.Ser1007=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39170 NM_198578.3(LRRK2):c.364C= (p.Leu122=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39180 NM_198578.3(LRRK2):c.4258G>A (p.Asp1420Asn) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39190 NM_198578.3(LRRK2):c.4448G>A (p.Arg1483Gln) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+dbSNP:rs34778348 rs34778348-? NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:12333 TH, -70G-A NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:13508 NM_002693.2(POLG):c.2869G>T (p.Ala957Ser) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:21866 NM_199292.2(TH):c.334G>A (p.Val112Met) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39185 NM_198578.3(LRRK2):c.4324G>C (p.Ala1442Pro) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39195 NM_198578.3(LRRK2):c.4793T>A (p.Val1598Glu) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39145 NM_198578.3(LRRK2):c.2147C>T (p.Ala716Val) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39135 NM_198578.3(LRRK2):c.1517G>A (p.Arg506Gln) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39175 NM_198578.3(LRRK2):c.3974G>A (p.Arg1325Gln) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39165 NM_198578.3(LRRK2):c.3451G>A (p.Ala1151Thr) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39155 NM_198578.3(LRRK2):c.2830G>T (p.Asp944Tyr) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39205 NM_198578.3(LRRK2):c.5174G>A (p.Arg1725Gln) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39245 NM_198578.3(LRRK2):c.894T>C (p.Ala298=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39215 NM_198578.3(LRRK2):c.5620G>T (p.Glu1874Ter) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39225 NM_198578.3(LRRK2):c.6415T>A (p.Cys2139Ser) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39235 NM_198578.3(LRRK2):c.7168G>A (p.Val2390Met) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:30834 NM_022089.3(ATP13A2):c.2552_2553delTT (p.Phe851Cysfs) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:12328 NM_199292.2(TH):c.1010G>A (p.Arg337His) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:754 NM_015575.3(GIGYF2):c.1370A>C (p.Asn457Thr) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:1220 ATP13A2, 22-BP DUP NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:13496 NM_002693.2(POLG):c.1399G>A (p.Ala467Thr) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:143196 NM_022089.3(ATP13A2):c.490C>T (p.Arg164Trp) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:66099 NM_022089.3(ATP13A2):c.2629G>A (p.Gly877Arg) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:1942 NM_198578.3(LRRK2):c.4322G>A (p.Arg1441His) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9283 NM_000161.2(GCH1):c.671A>G (p.Lys224Arg) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9273 GCH1, 2-BP INS NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9288 NM_000161.2(GCH1):c.142C>T (p.Gln48Ter) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9278 NM_000161.2(GCH1):c.431A>C (p.His144Pro) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39148 NM_198578.3(LRRK2):c.2264C>T (p.Pro755Leu) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39138 NM_198578.3(LRRK2):c.1630A>G (p.Lys544Glu) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39128 NM_198578.3(LRRK2):c.1000G>A (p.Glu334Lys) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39178 NM_198578.3(LRRK2):c.4193G>A (p.Arg1398His) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39168 NM_198578.3(LRRK2):c.3574A>G (p.Ile1192Val) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39158 NM_198578.3(LRRK2):c.2918G>A (p.Ser973Asn) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39198 NM_198578.3(LRRK2):c.4883G>C (p.Arg1628Pro) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39188 NM_198578.3(LRRK2):c.4364_4365delAT (p.Asp1455Glyfs) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39278 NM_198578.3(LRRK2):c.6523G>C (p.Asp2175His) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39228 NM_198578.3(LRRK2):c.6510C>A (p.Gly2170=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39218 NM_198578.3(LRRK2):c.6035T>C (p.Ile2012Thr) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39238 NM_198578.3(LRRK2):c.7190T= (p.Met2397=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39208 NM_198578.3(LRRK2):c.5385G>T (p.Leu1795Phe) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:13514 NM_002693.2(POLG):c.1532G>A (p.Ser511Asn) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:12326 NM_199292.2(TH):c.1481C>T (p.Thr494Met) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39213 NM_198578.3(LRRK2):c.5606T>C (p.Met1869Thr) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39203 NM_198578.3(LRRK2):c.5163A>G (p.Ser1721=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39243 NM_198578.3(LRRK2):c.825T= (p.His275=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39233 NM_198578.3(LRRK2):c.713A>T (p.Asn238Ile) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39223 NM_198578.3(LRRK2):c.632C>T (p.Ala211Val) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39173 NM_198578.3(LRRK2):c.3784C>G (p.Pro1262Ala) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39163 NM_198578.3(LRRK2):c.3333G>T (p.Gln1111His) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39183 NM_198578.3(LRRK2):c.4309A>C (p.Asn1437His) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39193 NM_198578.3(LRRK2):c.4624C>T (p.Pro1542Ser) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39143 NM_198578.3(LRRK2):c.2022A>C (p.Val674=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39133 NM_198578.3(LRRK2):c.1464A>T (p.Leu488=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39153 NM_198578.3(LRRK2):c.2769G>C (p.Gln923His) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+dbSNP:rs34637584 rs34637584-A NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:757 NM_015575.3(GIGYF2):c.1262A>G (p.Lys421Arg) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000269 experimental evidence used in manual assertion PMID:18358451 http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9291 GCH1, DEL NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9271 NM_000161.2(GCH1):c.262C>T (p.Arg88Trp) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:12324 NM_199292.2(TH):c.1234C>A (p.Gln412Lys) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:12334 NM_199292.2(TH):c.1076G>T (p.Cys359Phe) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39231 NM_198578.3(LRRK2):c.683G>C (p.Cys228Ser) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39241 NM_198578.3(LRRK2):c.7435A>G (p.Asn2479Asp) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39201 NM_198578.3(LRRK2):c.4939T>A (p.Ser1647Thr) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39221 NM_198578.3(LRRK2):c.6241A>G (p.Asn2081Asp) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:39211 NM_198578.3(LRRK2):c.546A>G (p.Lys182=) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000501 evidence used in automatic assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:9276 GCH1, IVS2, A-G, -2 NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
+ClinVarVariant:208620 NM_000360.3(TH):c.283delG (p.Ala95Argfs) NCBITaxon:9606 Homo sapiens HP:0002548 Parkinsonism with favorable response to dopaminergic medication ECO:0000304 traceable author statement used in manual assertion http://data.monarchinitiative.org/ttl/clinvar.ttl|http://data.monarchinitiative.org/ttl/hpoa.ttl inferred
diff -r 000000000000 -r 850bb90bd667 test-data/variants-for-phenotypes-intersection.tsv
--- /dev/null Thu Jan 01 00:00:00 1970 +0000
+++ b/test-data/variants-for-phenotypes-intersection.tsv Sun Jun 26 16:00:28 2016 -0400
@@ -0,0 +1,329 @@
+MGI:3512173 Grin3b MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17880385 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3578225 Gsk3a MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20357757 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3815322 Gt(ROSA)26Sor MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21885734 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4868760 Atmin MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20889973 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3640817 Ntrk2 MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:19158294|PMID:19158294 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4359727 Dp(7Herc2-Mkrn3)1Taku NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19563756 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2178959 Mdk MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10096022 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3720069 Tg(Thy1-App*R609D*K612E)6Vln NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:8635459|PMID:8635459 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2183727 Mecp2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12160743 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1856716 Myo7a MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:63673 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3603321 Grm8 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16045496 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2386577 Pax5 MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:23349049|PMID:23349049 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3513042 Crhbp RO:0002200 has phenotype MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:10500222|PMID:10500222 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3834477 Slitrk1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18794888 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4949899 Fgfbp3 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20851768 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3528874 Kcnip3 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19223600 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3042719 Nrxn2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:25423136 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3835761 Wfs1 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19477223 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5052110 Tg(Mapt-MAPT*)#Hanr NCBITaxon:10090 Mus musculus NCBIGene:4137 microtubule associated protein tau MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18490011 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2181809 Lgals1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23118208 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3575505 Ehmt1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19896504 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3530090 B4galt5 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3609573 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3798957 Del(16Dgcr2-Hira)3Aam NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18469815 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1928960 Dbh MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16723393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5317120 Del(5Gtf2i-Limk1)1Uta NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20049703 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4443321 Grin2b MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20357110 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3692441 Grin1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19915563 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3696469 Tg(Prnp-App/APPswe)E1-2Dbo NCBITaxon:10090 Mus musculus NCBIGene:351 APP RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9117892|PMID:12742740|PMID:12742740 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3653645 Nkx2-1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17182767 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2176054 Tg(Syn1-cre)671Jxm NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17182767 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4353991 Skap2 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24815314|PMID:16135797 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:1857197 Il6 MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:16843000|PMID:12946594|PMID:19378383 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2451031 Cacna1e MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:11854466 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3055492 Bbs4 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16794820 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2388359 Folh1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16190866 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3613512 Tg(YAC128)53Hay NCBITaxon:10090 Mus musculus NCBIGene:3064 huntingtin MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19464370 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5285394 Shank3 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:24652766 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2387408 Htr1a MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:10751426|PMID:9724773|PMID:9724773 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2449922 Fev MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20818386 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4418483 Tg(tetO-APBA2,-lacZ)1Ito NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19420255 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4452483 Tg(Prnp-ITM2B*)7Jckr NCBITaxon:10090 Mus musculus NCBIGene:9445 integral membrane protein 2B MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20385796 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5317543 Gpr26 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:21924326 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3811718 Npy MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18616565 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1930937 Psen1 MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:22336193|PMID:24278307 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3764690 Park2 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:17883413 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3526452 Spred1 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19118178 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3774541 Tph2 MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:18212115|PMID:18212115 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2388040 Map6 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12231625 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3590684 Pvalb MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24430185 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2384087 Fshr MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:14502087 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2182322 Gtf2ird1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22652393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3762757 Shank1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18272690 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2384535 Cckbr MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12459512 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3051945 Slc17a7 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17241289 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3800752 Tg(HTT*97Q)IXwy NCBITaxon:10090 Mus musculus NCBIGene:3064 huntingtin MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23001568 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3578226 Gsk3b MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20357757 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4949738 Shank3 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21423165 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2388370 Tnc MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16553788 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2177646 Tg(Camk2a-cre)T29-1Stl NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20357110 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4452483 Tg(Prnp-ITM2B*)7Jckr NCBITaxon:10090 Mus musculus NCBIGene:9445 integral membrane protein 2B MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20385796 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4867226 Grn MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22062772 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3050759 Rasd2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15199135 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3573912 Aaj3 MP:0001363 increased anxiety-related response ECO:0000304 traceable author statement used in manual assertion PMID:15371360 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2159000 Oprm1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22231481 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3487250 Dp(16Cbr1-Fam3b)1Rhr NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19420260 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4168877 Tmem43 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20562862|MGI:3510987 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:5560820 Mpst MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23759691 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3759300 Dlgap3 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17713528 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1857129 Apoe RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:15304509|PMID:10684907|PMID:15708438|PMID:15708438 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:5296970 Fkbp5 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21935478 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2387957 Kcnc2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11124984 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2673210 Npepps MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:10407043 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2177766 Tg(Camk2a-cre)1Szi NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22174697 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3764690 Park2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17883413 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2388020 Penk MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11172058 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3604604 Lrp5 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4461457 Tg(RP23-326M22)760She NCBITaxon:10090 Mus musculus RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:18285828|PMID:18285828|PMID:18285828 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:2386761 Esr2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11593044 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2447591 Tg(APP)8.9Btla NCBITaxon:10090 Mus musculus NCBIGene:351 APP MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15016076 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3718452 Tg(SOD1)51Yg NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15016076 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4819832 Tg(tetO-MAPT*P301L)#Kha NCBITaxon:10090 Mus musculus NCBIGene:4137 microtubule associated protein tau MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24503275 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1933974 Ntrk2 MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:18832146|PMID:10571233 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5516082 Slc6a2 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23580201 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3707315 Cadps2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17380209 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3757650 Arhgef9 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17690689 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1857736 Cnr1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15078564|PMID:11823890|PMID:12405999 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4421502 Tg(Ppp1r2-cre)4127Nkza NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19915563 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3513042 Crhbp RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10500222|PMID:10500222 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:5553462 Tg(Prnp-APPSweArc)#Rmni NCBITaxon:10090 Mus musculus NCBIGene:351 APP MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16876915 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1861234 Wt NCBITaxon:10090 Mus musculus MGI:1861234 Wt MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:13834122 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2387415 Hrh3 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15078574 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2178542 Comt MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9707588 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3844445 Tg(Thy1-Nlgn2)6Hnes NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18550748 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5509054 Uba6 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23499007 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3510602 Tg(Thy1-APP)28Lpr NCBITaxon:10090 Mus musculus NCBIGene:351 APP MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18184372 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5644306 Baiap3 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23698091 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3762883 Slc12a5 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15813942 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3692442 Rgs9 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24784230 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5297824 Lrrc7 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22072671 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5587996 Tg(Gpr151-cre)#Ito NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23487260 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5516082 Slc6a2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23580201 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3611335 Gria2 MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:16216087|PMID:16099814 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2447863 Gjb6 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12911759 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2177174 Tg(Eno2-cre)39Jme NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16675393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2386761 Esr2 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:11593044 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3522476 Als2 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16107644|PMID:16107644 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3605006 Efna3 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:25281279 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3664862 Bdnf MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17023662 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2176750 Bdnf MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11579207 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5007226 Lrrn1 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:5000289|PMID:20562862 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:2388945 Ctns MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12370309 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1857158 Drd1 MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:10884517|PMID:10884517 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5559062 Nenf MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24058337 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3579440 Gabrg2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15850489 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3057337 Maoa MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15272015 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3829789 Tg(YAC18)18Hay NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23001568 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5085894 Emc10 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20562862|MGI:3510987 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3604469 Kcnh5 RO:0002200 has phenotype MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3815538 Tg(MECP2)3Hzo NCBITaxon:10090 Mus musculus NCBIGene:4204 MECP2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22231481 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5521184 Tg(Thy1-Tcf4)1Mjro NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20434134 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5298021 Gria4 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20662939 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3822008 Vnhv2 MP:0002797 increased thigmotaxis ECO:0000304 traceable author statement used in manual assertion PMID:18721828 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5638435 Slc12a5 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15813942 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2176186 Tg(Zp3-cre)93Knw NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18320030 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4421502 Tg(Ppp1r2-cre)4127Nkza NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19915563 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5549960 Atat1 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23748901 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1861932 Gt(ROSA)26Sor MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:18832146 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3775204 S100a10 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16400147 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2154522 App MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:17634375|PMID:8001115 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5317121 Del(5Limk1-Trim50)2Uta NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20049703 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2179191 Tbx1 RO:0002200 has phenotype MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:15084464|PMID:21908517|PMID:11239417|PMID:12413905 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:2653694 Tnf MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11063830 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2388099 Sstr2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11029646 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3610995 Gabbr2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15706241 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4459459 Slitrk5 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20418887 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3573908 Aaj1 MP:0001363 increased anxiety-related response ECO:0000304 traceable author statement used in manual assertion PMID:15371360 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2387410 Htr1a MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:9844013|PMID:9844013 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1934210 Plaur MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12533622 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2673210 Npepps MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10407043 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1857026 Foxq1 MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:16109771|PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4438230 Tg(HTT*)1Xwy NCBITaxon:10090 Mus musculus NCBIGene:3064 huntingtin MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20064390 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5575506 Tg(Prnp-SNAP25/HTT*150Q)8Xjl NCBITaxon:10090 Mus musculus NCBIGene:3064 huntingtin MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24081492 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4261988 Sppl3 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20562862|PMID:20562862 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3765961 Eno2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23487260 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2158808 Mas1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9565612 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2178616 Crhr2 MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:10742109|PMID:10742109 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3528558 Csmd1 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24244513 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:2178057 Gria1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20699120 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2384087 Fshr MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:14502087 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3665437 Fabp7 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16882015 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1857159 Drd3 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:10884517 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3057129 Tg(MAPT)8cPdav NCBITaxon:10090 Mus musculus NCBIGene:4137 microtubule associated protein tau MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24278307 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4417910 Tg(Thy1-PSEN1*M146V,-APP*Swe)10Arte NCBITaxon:10090 Mus musculus NCBIGene:351 APP MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19936202 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2136456 Penk-rs MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:8849726 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2182005 Pten MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16675393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2387013 Oprd1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10835636 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3604527 Cacna1c MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3844445 Tg(Thy1-Nlgn2)6Hnes NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:18550748 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5644306 Baiap3 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23698091 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3526160 Rai1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17517686 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5486475 Tg(Gad1-cre,-lacZ)1Mini NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:23349049|PMID:23349049 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2449922 Fev MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:12546819|PMID:20818386 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3043746 Igf2bp1 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3609573 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3027491 Htr4 MP:0001363 increased anxiety-related response ECO:0000304 traceable author statement used in manual assertion PMID:14724239 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4462822 Del(7Slx1b-Sept1)4Aam NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:25698753 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5288003 Dcdc2a MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21883923 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4359176 Arx MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19605412 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4443014 Bdnf MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20130183 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5427678 Mc2r MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:2655403 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3821974 Snap25 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19043548 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5317543 Gpr26 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21924326 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2386951 Tg(HDexon1)62Gpb NCBITaxon:10090 Mus musculus NCBIGene:3064 huntingtin MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:19464370|PMID:19464370 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3762618 Grn MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17764761 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2679626 Cplx2 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20412316 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3604494 Gpr19 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3625122 Ids MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16505002 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4442238 Chd6 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20111866 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2384136 Ucn MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:12091910 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3692441 Grin1 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19915563 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3827095 Scn8a MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19737145 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4837197 Fev MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20818386 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4867464 Nlgn3 MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:19360662|PMID:19360662 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3578225 Gsk3a MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20357757 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2182936 Slc18a2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19553450 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2686971 Anxty MP:0001363 increased anxiety-related response ECO:0000304|ECO:0000304 traceable author statement used in manual assertion|traceable author statement used in manual assertion PMID:12719372|PMID:12719372 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3757650 Arhgef9 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:17690689 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3696979 Tg(Fev-cre)1Esd NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21885734 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2176751 Tg(Camk2a-cre)159Kln NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:10571233 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5085889 Lrrtm1 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:21818371 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3773671 Snord116 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18320030 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3712115 Tg(Camk2a-Crebbp*)1364Tabe NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:15805310 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2385822 Hsd17b4 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23777740 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3522468 Ppargc1a MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:15760270 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2159352 Gabbr1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15321743|PMID:15706241 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3815539 Tg(MECP2)1Hzo NCBITaxon:10090 Mus musculus NCBIGene:4204 MECP2 MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:22231481|PMID:22231481 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5297219 Snap25 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:21949876 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1888964 Chrna4 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10964949 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2182943 Efna2 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:25281279 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4414758 Myg1 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19818808 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2183719 Tg(SOD1*G93A)1Gur NCBITaxon:10090 Mus musculus NCBIGene:6647 superoxide dismutase 1, soluble MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16737688 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4410507 Rnf103 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19753093|PMID:18958194|PMID:18958194 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3840549 Lypd1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19246390 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2678096 Crhr1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21885734 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5495768 Dlg4 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23268962 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5523923 Hsd17b4 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23777740 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5608589 Hprt NCBITaxon:10116 Rattus norvegicus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24430185 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2686951 Hcn1 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:14651847 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4429408 Pitx3 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20033184 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3778285 Tg(DRD1-ctxA)7Burt NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10780249 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3612428 Tg(Gnrh1-cre)1Rsp NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16099814 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1929986 Bdnf MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17023662 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4837202 Tg(Fev-cre/ERT2)aEsd NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20818386 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2176219 Emx1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22726441 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3604447 Ulk2 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3609573 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:5544724 Gbx1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24010020 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3778285 Tg(DRD1-ctxA)7Burt NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:10780249 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4440439 Tg(CAG-VCP*R155H)55Jpat NCBITaxon:10090 Mus musculus NCBIGene:7415 VCP MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20147319 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2136456 Penk-rs MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:8849726 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2180752 Maob MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15272015 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2177567 Gad2 MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:10814732|PMID:10814732 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5515451 M876b NCBITaxon:10090 Mus musculus MGI:5515451 M876b MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3608888 Ric8 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16221497 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3512756 Mapt MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20130183 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3528558 Csmd1 RO:0002200 has phenotype MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:24244513 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3821974 Snap25 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19043548 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3697454 Apba2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19420255 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5634957 Fosb MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21679928 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3530009 Atp1a1 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3609573 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:4837197 Fev MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:20818386 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2176172 Tg(Nes-cre)1Kln NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:23777740|PMID:20889973 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3763533 Trhr MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17666589 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2180136 Adora1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11470917 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5523992 Cnr1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23785142 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3759303 Tg(Camk2a-cre/ERT2)2Gsc NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21885734 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3505768 Tg(Tuba1-cre)1Tes NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18723674 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3811632 Adm MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18723674 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3822325 Slc2a3 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18780771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2159003 Nos3 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10964974 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5620796 Tg(Camk2a-Magi2)1Shlee NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:25653350 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3835761 Wfs1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19477223 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2177743 Htt MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23001568 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3573914 Aaj4 MP:0001363 increased anxiety-related response ECO:0000304 traceable author statement used in manual assertion PMID:15371360 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2176752 Tg(Camk2a-cre)93Kln NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11579207 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3577248 Dp(11Cops3-Rnf112)1Jrl NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18469339 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5312129 Xpa MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22174697 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3819793 Sox4 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3603303 Thra MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16131613 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3822005 Vnhv1 MP:0002797 increased thigmotaxis ECO:0000304 traceable author statement used in manual assertion PMID:18721828 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2181421 Tg(Camk2a-cre)1Gsc NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16216087 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3717174 Tg(Eno2-APOE_i4)1Rabr NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15708438 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4359177 Arx MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19605412 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4837202 Tg(Fev-cre/ERT2)aEsd NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20818386 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1932102 Ercc6 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22174697 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2178821 Kcnj11 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16530794 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1857129 Apoe RO:0002200 has phenotype MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:15304509|PMID:12220566 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3604536 Cer1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3604450 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5313432 Vamp7 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22323709 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3802585 Crem MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18562617 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1934018 Naglu MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10588735 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2386303 Slc6a3 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:12617953 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1861926 Gabrd MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18667149 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2179062 Tg(Camk2a-tTA)1Mmay NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:22084082|PMID:19420255|PMID:24503275 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2176172 Tg(Nes-cre)1Kln NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23499007 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5437479 Shank2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22699620 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3618114 H2-K MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10386391 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5562642 Cpeb3 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24155305 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3043293 Mapt MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22378884 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5495816 Ddc MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23275025 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3809545 Tg(RCAN1)M9Mapr NCBITaxon:10090 Mus musculus NCBIGene:1827 RCAN1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22511596 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2176236 Idua MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18022143 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5435698 Shank2 MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:22699619|PMID:22699619 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3773673 Snord116 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:3774147 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2387407 Htr1a MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:20152131|PMID:9826725|PMID:9826725 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2152217 Esr2 RO:0002200 has phenotype MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15642619|PMID:9861029|PMID:8248223 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:5307897 Npy1r MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22084082 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2388945 Ctns MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:12370309 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3857785 Epm2aip1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24142699 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2177174 Tg(Eno2-cre)39Jme NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16675393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3612429 Tg(Gria2*586N)238.2Rsp NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15827116 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1857443 L1cam MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:9580664 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4438917 Srr MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:19065142 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4950685 Dync1li1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21471385 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3573910 Aaj2 MP:0001363 increased anxiety-related response ECO:0000304 traceable author statement used in manual assertion PMID:15371360 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1857169 Fmr1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19016890 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2182618 Hdc MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16412995|PMID:16310870 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4421144 Atf7 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19893493 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5308748 Bhv31 NCBITaxon:10090 Mus musculus MGI:5308748 Bhv31 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence MGI:4940633 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2449464 Ntan1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10805755 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2384136 Ucn MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:12091910 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5550580 Tg(PDGFB-APPInd)F17Plhn NCBITaxon:10090 Mus musculus NCBIGene:351 APP MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:16289866 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4440440 Tg(CAG-VCP*A232E)93Jpat NCBITaxon:10090 Mus musculus NCBIGene:7415 VCP MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20147319 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1857939 Xpa MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:22174697 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5495816 Ddc MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23275025 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3757609 Ophn1 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:17728457 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5433221 Fgf13 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22726441 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5568206 Mecp2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:24283265 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3830051 Slc1a3 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:18832146 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2448952 Tg(tetO-cre)LC1Bjd NCBITaxon:10090 Mus musculus MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:22084082 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2178545 Crhr2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:10742108 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5297219 Snap25 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:21949876 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3828099 Npas4 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:18815592 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2387410 Htr1a MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:9844013 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:4355536 mt-Atp8 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:19037013 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2158758 Chrna4 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11226318 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2451291 Atp1a2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17234593 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1857814 Ntrk2 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:10571233 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3578226 Gsk3b MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20357757 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2686972 Anxty MP:0001363 increased anxiety-related response ECO:0000304 traceable author statement used in manual assertion PMID:12719372 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2385631 Tg(APPSWE)2576Kha NCBITaxon:10090 Mus musculus NCBIGene:351 APP RO:0002200 has phenotype MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:9302276|PMID:16260491 http://data.monarchinitiative.org/ttl/mgi.ttl|http://data.monarchinitiative.org/ttl/mmrrc.ttl direct
+MGI:3527166 Th MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16723393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3720068 Tg(Thy1-App*R609D*K612E)4Vln NCBITaxon:10090 Mus musculus MP:0002797 increased thigmotaxis ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:8635459|PMID:8635459 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3609234 App MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006|ECO:0000006 experimental evidence|experimental evidence|experimental evidence PMID:22336193|PMID:22336193|PMID:24278307 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5568123 Sv2c MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23458503 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5634938 Tg(Thy1-EGFP/SQSTM1*P392L)#Mcwo NCBITaxon:10090 Mus musculus NCBIGene:8878 sequestosome 1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23591541 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1857026 Foxq1 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1857572 Ins2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:17334640 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3607718 sau NCBITaxon:10090 Mus musculus MGI:3607718 sau MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16109771 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2152583 Adora2a MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9262401 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1931877 Vim MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:9888296 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3800752 Tg(HTT*97Q)IXwy NCBITaxon:10090 Mus musculus NCBIGene:3064 huntingtin MP:0001363 increased anxiety-related response ECO:0000006|ECO:0000006 experimental evidence|experimental evidence PMID:19464370|PMID:24784230|PMID:20064390|PMID:24784230 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5503119 Kif13a MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:23438369 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3759300 Dlgap3 MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:17713528 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2388144 Rgs2 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:11027316 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:1857227 Nos1 MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:15158692 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:2182005 Pten MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:16675393 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5532204 Gtf2i MP:0001363 increased anxiety-related response ECO:0000006 experimental evidence PMID:20403157 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:5503119 Kif13a MP:0002797 increased thigmotaxis ECO:0000006 experimental evidence PMID:23438369 http://data.monarchinitiative.org/ttl/mgi.ttl inferred
+MGI:3604467 Prss12