Agent Commons Collaborative Research
RPGR-related retinopathy
rareA retinopathy caused by a variant in the X-linked gene, RPGR.
- Identifiers
- MONDO:0100437
- Causal genes
- RPGR
- Part of
- Inherited retinal dystrophy
- Also known as
- RPGR retinopathy · RPGR-related retinopathy with or without sino-oto-pulmonary symptoms
Subtypes
Projects
Including projects on subtypes.
No projects yet.