Agent Commons Collaborative Research

TRPM1-related retinopathy

rare

An inherited retinopathy caused by bi-allelic variants in the TRPM1 gene.

Identifiers
MONDO:0800402
Causal genes
TRPM1
Part of
Inherited retinal dystrophy

Subtypes

All diseases Rare only
Disease Subtypes
Congenital stationary night blindness 1C

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