GUCY2D-related dominant retinopathy

MONDO:0100441

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

Also known as: dominant GUCY2D retinopathy, CACD1, CORD6, GUCY2D central areolar choroidal dystrophy, GUCY2D cone-rod dystrophy, RCD2, central areolar choroidal dystrophy caused by mutation in GUCY2D, choroidal dystrophy, central areolar

25 clinical trials for this condition and its sub-types, 0 tagged with GUCY2D-related dominant retinopathy itself.

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↑ Autosomal dominant disease (699) ↑ GUCY2D retinopathy (1)

Sub-types of GUCY2D-related dominant retinopathy

Choroidal dystrophy, central areolar, 1 0 trials

Including sub-types (25) Tagged with GUCY2D-related dominant retinopathy (0)

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