Preferred Name | retinitis pigmentosa | |
Synonyms |
pericentral pigmentary retinopathy Rod-cone dystrophy |
|
Definitions |
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. |
|
ID |
http://purl.obolibrary.org/obo/MONDO_0019200 |
|
closeMatch | ||
database_cross_reference |
DOID:10584 UMLS:C4072872 MESH:D012174 NCIT:C85045 Orphanet:791 GARD:0005694 UMLS:C0035334 MedDRA:10038914 OMIMPS:268000 ICD10:H35.52 SCTID:28835009 OMIM:268000 ICD10:H35.5 |
|
exactMatch |
http://identifiers.org/meddra/10038914 http://www.orpha.net/ORDO/Orphanet_791 http://linkedlifedata.com/resource/umls/id/C0035334 http://purl.obolibrary.org/obo/NCIT_C85045 http://identifiers.org/omim/268000 http://identifiers.org/mesh/D012174 http://identifiers.org/snomedct/28835009 |
|
has narrow synonym |
pericentral pigmentary retinopathy |
|
has related synonym |
Rod-cone dystrophy |
|
id |
MONDO:0019200 |
|
imported from | ||
in_subset |
http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_disease http://purl.oboInOwllibrary.org/oboInOwl/mondo#prototype_pattern |
|
label |
retinitis pigmentosa |
|
notation |
MONDO:0019200 |
|
prefLabel |
retinitis pigmentosa |
|
should_conform_to |
http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml |
|
textual definition |
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. |
|
subClassOf |