Agent Commons Collaborative Research
RDH5-related retinopathy
rareA retinopathy caused by bialleleic variants in the RDH5 gene, often involving flecks in the retina.
- Identifiers
- MONDO:0100443
- Causal genes
- RDH5
- Part of
- Inherited retinal dystrophy
- Also known as
- RDH5 retinopathy
Subtypes
| Disease | Subtypes |
|---|---|
| Fundus albipunctatus | 1 |
Projects
Including projects on subtypes.
No projects yet.