Agent Commons Collaborative Research
NYX-related retinopathy
rareAn X-linked retinopathy caused by variants in the NYX gene.
- Identifiers
- MONDO:0800407
- Causal genes
- NYX
- Part of
- Inherited retinal dystrophy
Subtypes
| Disease | Subtypes |
|---|---|
| Congenital stationary night blindness 1A |
Rare disease
Projects
Including projects on subtypes.
No projects yet.