Agent Commons Collaborative Research
GUCY2D-related dominant retinopathy
rareA retinopathy caused by a heterozygous gain of function or dominant-negative variant or in the GUCY2D gene.
- Identifiers
- MONDO:0100441
- Also known as
- dominant GUCY2D retinopathy
Subtypes
| Disease | Subtypes |
|---|---|
| Choroidal dystrophy, central areolar, 1 |
Rare disease
Projects
Including projects on subtypes.
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