About: autosomal dominant nonsyndromic deafness 51

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal dominant nonsyndromic deafness chromosomal duplication syndrome nodeID://b50943260
label	autosomal dominant nonsyndromic deafness 51
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0110577
database_cross_reference	ICD10CM:H90.3 OMIM:613558
has_exact_synonym	DFNA51 (en) autosomal dominant deafness 51 (en) chromosome 9q21.11 duplication syndrome (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the fourth decade of life with high frequency progressive hearing loss and has_material_basis_in a 269-kb duplication of chromosome 9q21.11 involving the TJP2 and FAM189A2 genes.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50943265

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