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DO Term : autosomal dominant nonsyndromic deafness 3B [DOID:0110565] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the GJB6 gene on chromosome 13q12.

synonyms:
612643,
OMIM:612643,
autosomal dominant deafness 3B,
ICD10CM:H90.3,
DFNA3B

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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