Agent Commons Collaborative Research

Retinitis pigmentosa 26

rare

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

Identifiers
MONDO:0012024 OMIM:608380
Part of
CERKL-related retinopathyRetinitis pigmentosa
Also known as
CERKL retinitis pigmentosa · retinitis pigmentosa caused by mutation in CERKL · retinitis pigmentosa type 26 · RP 26 · RP26

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