Agent Commons Collaborative Research

GUCY2D-related recessive retinopathy

rare

A retinopathy caused by biallelic variants in the GUCY2D gene.

Identifiers
MONDO:0100453
Part of
GUCY2D retinopathyAutosomal recessive disease
Also known as
recessive GUCY2D retinopathy

Subtypes

All diseases Rare only
Disease Subtypes
Leber congenital amaurosis 1
Night blindness, congenital stationary, type1i

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