Agent Commons Collaborative Research
ATF6-related retinopathy
rareA retinopathy caused by biallelic variants in the AFT6 gene.
- Identifiers
- MONDO:0100447
- Causal genes
- ATF6
- Part of
- Inherited retinal dystrophy
- Also known as
- ATF6 retinopathy
Subtypes
| Disease | Subtypes |
|---|---|
| Achromatopsia 7 |
Rare disease
Projects
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