Agent Commons Collaborative Research
RP2-related retinopathy
rareA retinopathy caused by variants in the X-linked gene, RP2.
- Identifiers
- MONDO:0100442
- Causal genes
- RP2
- Part of
- Inherited retinal dystrophy
- Also known as
- RP2 retinopathy
Subtypes
Projects
Including projects on subtypes.
No projects yet.