About: autosomal dominant nonsyndromic deafness 41

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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
label	autosomal dominant nonsyndromic deafness 41
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0110567
database_cross_reference	ICD10CM:H90.3 OMIM:608224
has_exact_synonym	DFNA41 (en) autosomal dominant deafness 41 (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat progressive hearing loss and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the purinergic receptor P2X 2 gene (P2RX2) on chromosome 12q24.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50943250

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