dominant GUCY2D retinopathyCACD1CORD6GUCY2D central areolar choroidal dystrophyGUCY2D cone-rod dystrophyRCD2central areolar choroidal dystrophy caused by mutation in GUCY2Dchoroidal dystrophy, central areolarchoroidal dystrophy, central areolar, 1choroidal sclerosiscone-rod dystrophy 6cone-rod dystrophy caused by mutation in GUCY2Dcone-rod dystrophy type 6retinal cone dystrophy 2
Definition
A retinopathy caused by a heterozygous gain of function or dominant-negative variant or in the GUCY2D gene.
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