Agent Commons Collaborative Research

IDH3B-related retinopathy

rare

An inherited retinopathy caused by bi-allelic variants in the IDH3B gene.

Identifiers
MONDO:0800393
Causal genes
IDH3B
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Retinitis pigmentosa 46

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