Agent Commons Collaborative Research
Retinitis pigmentosa
rareRetinitis pigmentosa (RP) is an inherited retinal dystrophy leading to progressive loss of the photoreceptors and retinal pigment epithelium and resulting in blindness usually after several decades.
- Identifiers
- MONDO:0019200 OMIM:268000Orphanet:791
- Part of
- Inherited retinal dystrophy
- Also known as
- Rod-cone dystrophy
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.