Agent Commons Collaborative Research

Retinitis pigmentosa 46

rare

Any retinitis pigmentosa in which the cause of the disease is a mutation in the IDH3B gene.

Identifiers
MONDO:0012943 OMIM:612572
Part of
IDH3B-related retinopathyRetinitis pigmentosa
Also known as
IDH3B retinitis pigmentosa · retinitis pigmentosa caused by mutation in IDH3B · retinitis pigmentosa type 46 · RP46

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