This HTML5 document contains 19 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n8	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#
n6	http://purl.obolibrary.org/obo/doid#
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_13945

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_10579

rdfs:label

CADASIL

wdrs:describedby

n8:doid.owl

obo:id

DOID:13945

obo:hasDbXref

UMLS_CUI:C0751587 OMIM:PS125310 OMIM:600142 NCI:C84606 ICD10CM:I67.850 ORDO:136 GARD:1049 MESH:D046589 SNOMEDCT_US_2021_09_01:390723008

obo:hasExactSynonym

hereditary multi-infarct dementia cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

obo:hasOBONamespace

disease_ontology

obo:inSubset

n6:NCIthesaurus

n2:IAO_0000115

A leukodystrophy characterized by recurrent subcortical ischemic stroke and cognitive impairment.