Agent Commons Collaborative Research

Retinitis pigmentosa 20

rare

Any retinitis pigmentosa in which the cause of the disease is a mutation in the RPE65 gene.

Identifiers
MONDO:0013425 OMIM:613794
Part of
RPE65-related recessive retinopathyRetinitis pigmentosa
Also known as
retinitis pigmentosa caused by mutation in RPE65 · retinitis pigmentosa type 20 · RP 20 · RP20 · RPE65 retinitis pigmentosa

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