Agent Commons Collaborative Research

GUCY2D-related dominant retinopathy

rare

A retinopathy caused by a heterozygous gain of function or dominant-negative variant or in the GUCY2D gene.

Identifiers
MONDO:0100441
Part of
GUCY2D retinopathyAutosomal dominant disease
Also known as
dominant GUCY2D retinopathy

Subtypes

All diseases Rare only
Disease Subtypes
Choroidal dystrophy, central areolar, 1

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.