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DO Term : autosomal recessive nonsyndromic deafness 37 [DOID:0110495] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14.

synonyms:
autosomal recessive deafness 37,
DFNB37,
ICD10CM:H90.3,
607821,
OMIM:607821

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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