Human Phenotype Ontology 
Grandparent Node:
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Abnormal fundus morphology (HP:0001098)help
Grandparent Node:
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Abnormal uvea morphology (HP:0000553)help
Parent Node:
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Abnormal choroid morphology (HP:0000610)help
..Starting node
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Dark choroid (HP:0025148)help
Term ID: 25148
Name: Dark choroid
Synonym:
Definition: A fluorescein angiographic finding of absence of the normal background fluorescence (a dark choroid).
Comments:
Reference: HP:0025148
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal chorioretinal morphology (HP:0000532) help
..expandAbnormal morphology of the choroidal vasculature (HP:0025568) help
..expandBirdshot retinochoroidopathy (HP:0030952) help
..expandChoroidal nevus (HP:0025314) help
..expandChoroideremia (HP:0001139) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025148HP:0025148Dark choroid0PRPH2 CL E G H59619942OMIM:169150Macular dystrophy, patterned, 1HP:0040283 - Occasional159


Genes (1) :PRPH2

Diseases (1) :OMIM:169150
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.