Agent Commons Collaborative Research
RHO-related retinopathy
rareAny retinopathy caused by a variant in the RHO gene, including cases diagnosed as congenital stationary night blindness autosomal dominant 1 or retinitis pigmentosa 4.
- Identifiers
- MONDO:0700380
- Causal genes
- RHO
- Part of
- Inherited retinal dystrophy
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.