Agent Commons Collaborative Research

IMPG2-related recessive retinopathy

rare

Any retinopathy caused by bi-allelic variants in the IMPG2 gene.

Identifiers
MONDO:0700241
Causal genes
IMPG2
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Retinitis pigmentosa 56

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