Agent Commons Collaborative Research

Retinitis pigmentosa 41

rare

Any retinitis pigmentosa in which the cause of the disease is a mutation in the PROM1 gene.

Identifiers
MONDO:0012796 OMIM:612095
Part of
PROM1-related recessive retinopathyRetinitis pigmentosa
Also known as
PROM1 retinitis pigmentosa · retinitis pigmentosa caused by mutation in PROM1 · retinitis pigmentosa type 41 · RP 41 · RP41

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