SPARQL | HTML Microdata document
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Namespace Prefixes
Prefix IRI
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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_0110543
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0050564
rdfs:label
autosomal dominant nonsyndromic deafness 11
wdrs:describedby
n5:doid.owl
obo:id
DOID:0110543
obo:hasDbXref
OMIM:601317
ICD10CM:H90.3
obo:hasExactSynonym
DFNA11
autosomal dominant deafness 11
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the MYO7A gene on chromosome 11q13.