Terminology Service for NFDI4Health
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retinitis pigmentosa

Go to external page http://purl.obolibrary.org/obo/MONDO_0019200

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. [ ]

Term info

Label

retinitis pigmentosa

Synonyms
  • retinitis pigmentosa
database cross reference
Subsets

ordo_disease, prototype_pattern, clingen

closeMatch

http://identifiers.org/meddra/10038914

exactMatch

http://identifiers.org/snomedct/28835009, http://identifiers.org/mesh/D012174, https://omim.org/entry/268000, http://linkedlifedata.com/resource/umls/id/C4072872, http://purl.obolibrary.org/obo/Orphanet_791, https://omim.org/phenotypicSeries/PS268000, http://linkedlifedata.com/resource/umls/id/C0035334, http://purl.obolibrary.org/obo/NCIT_C85045, http://purl.obolibrary.org/obo/DOID_10584

has narrow synonym

pericentral pigmentary retinopathy

has related synonym

Rod-cone dystrophy

id

MONDO:0019200