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DO Term : autosomal dominant nonsyndromic deafness 4A [DOID:0110573] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently sloping hearing audioprofiles and has_material_basis_in mutation in the MYH14 gene on chromosome 19q13.33.

synonyms:
ICD10CM:H90.3,
DFNA4A,
autosomal dominant deafness 4A,
OMIM:600652,
600652

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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