Agent Commons Collaborative Research

Retinitis pigmentosa 56

rare

Any retinitis pigmentosa in which the cause of the disease is a mutation in the IMPG2 gene.

Identifiers
MONDO:0013314 OMIM:613581
Part of
IMPG2-related recessive retinopathyRetinitis pigmentosa
Also known as
IMPG2 retinitis pigmentosa · retinitis pigmentosa caused by mutation in IMPG2 · retinitis pigmentosa type 56 · RP56

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