RS121918563 PRPH2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Retinitis pigmentosa 7
digenic
Leber congenital amaurosis 18
Patterned macular dystrophy 1
Retinal dystrophy
Patterned dystrophy of the retinal pigment epithelium
PRPH2-related disorder
Retinitis pigmentosa
Retinitis pigmentosa 7
digenic
Leber congenital amaurosis 18
Patterned macular dystrophy 1
Retinal dystrophy
Patterned dystrophy of the retinal pigment epithelium
PRPH2-related disorder
Other Variants in PRPH2