choroidal degeneration Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Degeneration of the choroid. (Human Phenotype Ontology, HP_0007945)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007945
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Genes

2 genes associated with the choroidal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHM choroideremia (Rab escort protein 1)
RP2 retinitis pigmentosa 2 (X-linked recessive)