Retinitis 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. [ Orphanet:791 ]
Synonyms: retinitis pigmentosa
Term information
- UMLS:C0035334 (Orphanet:791/e)
- ICD10CM:H35.5 (Orphanet:791/ntbt)
- GARD:5694 (Orphanet:791)
- OMIMPS:268000 (MONDO:equivalentTo)
- SCTID:28835009 (MONDO:equivalentTo)
- DOID:10584 (MONDO:equivalentTo)
- NCIT:C85045 (MONDO:equivalentTo)
- Orphanet:791 (MONDO:equivalentTo)
- NORD:1661 (MONDO:NORD)
- MESH:D012174 (Orphanet:791/e)
- OMIM:268000 (Orphanet:791/e)
- MedDRA:10038914 (Orphanet:791/e)
gard_rare, ordo_disease, rare, prototype_pattern, nord_rare, orphanet_rare
https://github.com/monarch-initiative/mondo/issues/5667
https://github.com/monarch-initiative/mondo/issues/4985
http://identifiers.org/snomedct/28835009
http://identifiers.org/mesh/D012174
https://omim.org/entry/268000
https://omim.org/phenotypicSeries/PS268000
http://purl.obolibrary.org/obo/NCIT_C85045
http://linkedlifedata.com/resource/umls/id/C0035334
http://www.orpha.net/ORDO/Orphanet_791
http://purl.obolibrary.org/obo/DOID_10584