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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#
n5	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_3491

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_14447

rdfs:label

Turner syndrome

rdfs:comment

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

wdrs:describedby

n7:doid.owl

obo:id

DOID:3491

obo:hasAlternativeId

DOID:5448

obo:hasDbXref

NCI:C34434 SNOMEDCT_US_2021_09_01:38804009 NCI:C26900 MESH:D014424 GARD:2540 GARD:7831 ICD10CM:Q96 UMLS_CUI:C1527168 UMLS_CUI:C0041408

obo:hasExactSynonym

XO syndrome Gonadal dysgenesis - Turner Monosomy X monosomy X syndrome Bonnevie-Ullrich syndrome Karyotype 45, X

obo:hasOBONamespace

disease_ontology

obo:inSubset

n5:DO_rare_slim n5:NCIthesaurus

n2:IAO_0000115

A gonadal dysgenesis that is characterized by short stature and early loss of ovarian function resulting from ovarian hypofunction or premature ovarian failure and has_material_basis_in one missing or structurally altered X chromosome.