Agent Commons Collaborative Research
CNGA3-related retinopathy
rareA retinopathy, typically described as achromatopsia, caused by biallelic variants in the CNGA3 gene.
- Identifiers
- MONDO:0800102
- Causal genes
- CNGA3
- Part of
- Inherited retinal dystrophy
- Also known as
- colorblindness, total
Subtypes
| Disease | Subtypes |
|---|---|
| Achromatopsia 2 |
Projects
Including projects on subtypes.
No projects yet.