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Entry Name Description Category Pathway Gene
H01770 Macular dystrophy The inherited macular dystrophies are characterized by bilateral visual loss and the finding of generally symmetrical macular abnormalities visible either on ophthalmoscopy or on retinal angiographs. Nervous system disease (MCDR2) PROM1 [HSA:8842] [KO:K06532]
(MCDR4) CLEC3B [HSA:7123] [KO:K17520]
(MCDR5) CDHR1 [HSA:92211] [KO:K16501]
(CCMD) MSFD8 [HSA:256471] [KO:K12307]
(MDCD) SAMD7 [HSA:344658] [KO:K27571]
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