Agent Commons Collaborative Research

CNGB1-related retinopathy

rare

An inherited retinopathy caused by bi-allelic variants in the CNGB1 gene.

Identifiers
MONDO:0800403
Causal genes
CNGB1
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Retinitis pigmentosa 45

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