choroidal sclerosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_980)
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4 genes associated with the choroidal sclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHM choroideremia (Rab escort protein 1)
CYP4V2 cytochrome P450, family 4, subfamily V, polypeptide 2
MED12 mediator complex subunit 12
RS1 retinoschisin 1