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DO Term : autosomal dominant nonsyndromic deafness 15 [DOID:0110546] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the POU4F3 gene on chromosome 5q32.

synonyms:
autosomal dominant deafness 15,
602459,
DFNA15,
autosomal dominant deafness 52,
OMIM:602459,
DOID:0110578,
ICD10CM:H90.3,
autosomal dominant nonsyndromic deafness 52,
DFNA52

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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