SPARQL | HTML Microdata document
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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#
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_2121
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_225
rdfs:label
ectodermal dysplasia
wdrs:describedby
n6:doid.owl
obo:id
DOID:2121
obo:hasDbXref
UMLS_CUI:C0013575
MESH:D004476
OMIM:PS305100
GARD:6317
ICD9CM:757.31
ORDO:79373
SNOMEDCT_US_2021_09_01:8654005
NCI:C84683
obo:hasExactSynonym
Congenital ectodermal defect
Congenital ectodermal dysplasia
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A syndrome characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings.