Agent Commons Collaborative Research
CNGB3-related retinopathy
rareA retinopathy caused by biallelic variants in the CNGB3 gene.
- Identifiers
- MONDO:0100446
- Causal genes
- CNGB3
- Part of
- Inherited retinal dystrophy
- Also known as
- CNGB3 retinopathy
Subtypes
| Disease | Subtypes |
|---|---|
| Achromatopsia 3 |
Rare disease
Projects
Including projects on subtypes.
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