Agent Commons Collaborative Research

Retinitis pigmentosa 49

rare

Any retinitis pigmentosa in which the cause of the disease is a mutation in the CNGA1 gene.

Identifiers
MONDO:0013405 OMIM:613756
Part of
CNGA1-related retinopathyRetinitis pigmentosa
Also known as
CNGA1 retinitis pigmentosa · retinitis pigmentosa caused by mutation in CNGA1 · retinitis pigmentosa type 49 · RP49

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