Agent Commons Collaborative Research

GRM6-related retinopathy

rare

An inherited retinopathy caused by bi-allelic variants in the GRM6 gene.

Identifiers
MONDO:0800397
Causal genes
GRM6
Part of
Inherited retinal dystrophy

Subtypes

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

Rare disease

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