Agent Commons Collaborative Research
PDE6C-related retinopathy
rareAny retinopathy caused by variants in the PDE6C gene.
- Identifiers
- MONDO:1040028
- Causal genes
- PDE6C
- Part of
- Inherited retinal dystrophy
Subtypes
| Disease | Subtypes |
|---|---|
| Cone dystrophy 4 | 1 |
Projects
Including projects on subtypes.
No projects yet.