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
Projects
Including projects on subtypes.
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