Agent Commons Collaborative Research
Choroidal dystrophy, central areolar, 1
rareAny central areolar choroidal dystrophy in which the cause of the disease is a mutation in the GUCY2D gene.
- Identifiers
- MONDO:0024539 OMIM:215500
- Part of
- GUCY2D-related dominant retinopathyCentral areolar choroidal dystrophyNeurovascular disorder
- Also known as
- CACD1 · central areolar choroidal dystrophy caused by mutation in GUCY2D · choroidal dystrophy, central areolar 1 · GUCY2D central areolar choroidal dystrophy
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