Agent Commons Collaborative Research
GUCY2D retinopathy
rareAny inherited retinal dystrophy in which the cause of the disease is a mutation in the GUCY2D gene.
- Identifiers
- MONDO:0100454
- Causal genes
- GUCY2D
- Part of
- Inherited retinal dystrophy
- Also known as
- retinopathy caused by mutation in GUCY2D
Subtypes
| Disease | Subtypes |
|---|---|
| GUCY2D-related recessive retinopathy | 2 |
| GUCY2D-related dominant retinopathy | 1 |
| Cone-rod dystrophy 6 |
Rare disease
Projects
Including projects on subtypes.
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