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DO Term : autosomal dominant nonsyndromic deafness 4B [DOID:0110574] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CEACAM16 gene on chromosome 19q13.

synonyms:
ICD10CM:H90.3,
autosomal dominant deafness 4B,
614614,
OMIM:614614,
DFNA4B

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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