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Namespace Prefixes

Prefix	IRI
n7	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
obo	http://www.geneontology.org/formats/oboInOwl#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item

n2:DOID_13080

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_417

rdfs:label

Jaccoud's syndrome

wdrs:describedby

n7:doid.owl

obo:id

DOID:13080

obo:hasDbXref

SNOMEDCT_US_2021_09_01:84801008 ICD10CM:M12.0 UMLS_CUI:C0152084 ICD9CM:714.4

obo:hasExactSynonym

Jaccoud syndrome

obo:hasOBONamespace

disease_ontology

n2:IAO_0000115

An autoimmune disease that is characterized by severe non-erosive arthropathy with ulnar deviation of the 2nd to 5th digits and metacarpophalangeal joint subluxation without evidence of synovitis, and may be associated with systemic lupus erythematosus, rheumatic fever, and ligamentous laxity.