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Diseases / Disease of genetic or genomic mechanism/ Hereditary disease/ Autosomal genetic disease/ Autosomal dominant disease

PROM1-related dominant retinopathy

rare

Any retinopathy caused by an autosomal dominant variant in the PROM1 gene.

Identifiers: MONDO:1040053
Part of: PROM1-related retinopathy Autosomal dominant disease

Subtypes

All diseases Rare only

Disease

Stargardt disease 4 MONDO:0011370
Retinal macular dystrophy type 2 MONDO:0011957

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