Experimental Factor Ontology

Last uploaded: November 18, 2024
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Preferred Name

retinitis pigmentosa
Synonyms

pericentral pigmentary retinopathy

Rod-cone dystrophy

retinitis pigmentosa
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

http://identifiers.org/meddra/10038914
database_cross_reference

ICD10CM:H35.5

Orphanet:791

MEDGEN:20551

MedDRA:10038914

SCTID:28835009

OMIM:268000

NCIT:C85045

OMIMPS:268000

UMLS:C0035334

NANDO:1200431

MESH:D012174

DOID:10584

GARD:5694

NORD:1661
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.
exactMatch

http://identifiers.org/medgen/20551

http://linkedlifedata.com/resource/umls/id/C0035334

https://omim.org/phenotypicSeries/PS268000

http://purl.obolibrary.org/obo/NCIT_C85045

http://purl.obolibrary.org/obo/Orphanet_791

http://identifiers.org/mesh/D012174

https://omim.org/entry/268000

http://identifiers.org/snomedct/28835009

http://purl.obolibrary.org/obo/DOID_10584
has_exact_synonym

retinitis pigmentosa
has_narrow_synonym

pericentral pigmentary retinopathy
has_related_synonym

Rod-cone dystrophy
IAO_0000233

https://github.com/monarch-initiative/mondo/issues/5667

https://github.com/monarch-initiative/mondo/issues/4985
id

MONDO:0019200
in_subset

http://purl.obolibrary.org/obo/mondo/mondo-base#rare

http://purl.obolibrary.org/obo/mondo/mondo-base#otar

http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare

http://purl.obolibrary.org/obo/mondo/mondo-base#orphanet_rare

http://purl.obolibrary.org/obo/mondo/mondo-base#nord_rare

http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_disorder

http://purl.obolibrary.org/obo/mondo/mondo-base#prototype_pattern
label

retinitis pigmentosa
notation

MONDO:0019200
preferred label

retinitis pigmentosa
prefLabel

retinitis pigmentosa
subClassOf

http://purl.obolibrary.org/obo/MONDO_0019216

http://purl.obolibrary.org/obo/MONDO_0019118
excluded_subClassOf

http://purl.obolibrary.org/obo/MONDO_0017688
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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0019200 CCONT SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019200 MONDO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019200 DOVES SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019200 KTAO SAME_URI
http://id.nlm.nih.gov/mesh/D012174 MDM LOOM
rgo:22660 GAMUTS LOOM
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:0349 IFAR LOOM
http://purl.bioontology.org/ontology/MEDDRA/10038914 MEDDRA LOOM
http://www.phoc.org.cn/pmo/class/PMO_00036607 PMAPP-PMO LOOM
http://purl.bioontology.org/ontology/CSP/1114-9526 CRISP LOOM
http://purl.bioontology.org/ontology/RCTV2/F427600 RCTV2 LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#10812 OCHV LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D012174 RH-MESH LOOM
http://www.orpha.net/ORDO/Orphanet_791 ORDO LOOM
http://purl.bioontology.org/ontology/MESH/D012174 MESH LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/28835009 SNOMEDCT LOOM
http://purl.obolibrary.org/obo/NCIT_C85045 BERO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.290.684 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C11.270.684 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C11.768.585.658.500 RH-MESH LOOM
http://purl.obolibrary.org/obo/MONDO_0019200 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0019200 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0019200 DOVES LOOM
http://purl.obolibrary.org/obo/MONDO_0019200 KTAO LOOM
http://nanbyodata.jp/ontology/NANDO_1200431 NANDO LOOM
http://www.semanticweb.org/hamide/ontologies/2019/3/IRD_1_1_1 HAMIDEHSGH LOOM
http://localhost/plosthes.2017-1#1907 PLOSTHES LOOM
http://purl.obolibrary.org/obo/OMIT_0013094 OMIT LOOM
http://identifiers.org/omim/268000 REXO LOOM
http://identifiers.org/omim/268000 GEXO LOOM
http://identifiers.org/omim/268000 RETO LOOM
http://purl.bioontology.org/ontology/OMIM/268000 OMIM LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU000322 OMIM LOOM
urn:agi-folder:retinitis_pigmentosa BPT LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C85045 NCIT LOOM
http://purl.bioontology.org/ontology/SNMI/DA-71906 SNMI LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12820 NIFDYS LOOM
http://uri.neuinfo.org/nif/nifstd/birnlex_12820 NIFSTD LOOM
http://www.limics.org/hrdo/rdfns#pat_id_659 HRDO LOOM
http://purl.bioontology.org/ontology/ICPC2P/F99053 ICPC2P LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_10584 NATPRO LOOM
http://bioontology.org/projects/ontologies/birnlex#birnlex_12820 BIRNLEX LOOM
http://purl.obolibrary.org/obo/DOID_10584 CLO LOOM
http://purl.obolibrary.org/obo/DOID_10584 DTO LOOM
http://purl.obolibrary.org/obo/DOID_10584 DOID LOOM
http://purl.obolibrary.org/obo/DOID_10584 BAO LOOM
http://purl.obolibrary.org/obo/DOID_10584 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_10584 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_10584 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_10584 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_10584 FNS-H LOOM
http://purl.org/obo/owl/HP#HP_0000510 BDO LOOM
http://purl.bioontology.org/ontology/RCD/F4276 RCD LOOM
http://purl.obolibrary.org/obo/OMIM_268000 CCO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Retinitis_Pigmentosa CSEO LOOM
http://www.semanticweb.org/hamide/ontologies/2019/3/IRD_1_1 HAMIDEHSGH LOOM
http://www.semanticweb.org/ontologies/2012/5/Ontology1338526551855.owl#Retinitis_pigmentosa RPO LOOM