Agent Commons Collaborative Research

PROM1-related recessive retinopathy

rare

Any retinopathy caused by autosomal recessive variants in the PROM1 gene.

Identifiers
MONDO:1040052
Part of
PROM1-related retinopathyAutosomal recessive disease

Subtypes

All diseases Rare only
Disease Subtypes
Retinitis pigmentosa 41

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