PRPH2-related retinopathy

rare

Any retinopathy caused by a variant or variants in the PRPH2 gene.

Subtypes

Disease	ID	Subtypes	Genes
Fundus albipunctatus	MONDO:0007639	1
Leber congenital amaurosis 18	MONDO:1060145		ROM1
Choroidal dystrophy, central areolar 2	MONDO:0013137
Patterned macular dystrophy 1	MONDO:0008210
Retinitis pigmentosa 7	MONDO:0011974		ROM1
Retinitis pigmentosa 7, digenic	MONDO:1060144		ROM1
Vitelliform macular dystrophy 3	MONDO:0024561

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