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DO Term : autosomal recessive nonsyndromic deafness 116 [DOID:0112162] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal recessive nonsyndromic deafness that has_material_basis_in homozygous or compound heterozygous mutation in the CLDN9 gene on chromosome 16p13.3.

synonyms:
DFNB116,
619093,
OMIM:619093

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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