Agent Commons Collaborative Research

IMPDH1-related retinopathy

rare

Any retinopathy caused by a variant in the IMPDH1 gene.

Identifiers
MONDO:1040051
Causal genes
IMPDH1
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Leber congenital amaurosis 11
Retinitis pigmentosa 10

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