This HTML5 document contains 21 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n6	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#
n7	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_1921

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_0060429

rdfs:label

Klinefelter syndrome

rdfs:comment

No OMIM mapping, confirmed by DO. [LS].

wdrs:describedby

n6:doid.owl

obo:id

DOID:1921

obo:hasDbXref

GARD:8705 UMLS_CUI:C0022735 SNOMEDCT_US_2021_09_01:405770005 ICD10CM:Q98.0 ICD9CM:758.7 NCI:C34752 MESH:D007713

obo:hasExactSynonym

XXY trisomy Klinefelter's syndrome 47, XXY Hypogonadotropic Hypogonadism XXY syndrome

obo:hasOBONamespace

disease_ontology

obo:inSubset

n7:NCIthesaurus

n2:IAO_0000115

A chromosomal duplication syndrome that is characterized by infertility and that has_material_basis_in an extra X chromosome in cells in men.