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DO Term : autosomal recessive nonsyndromic deafness 2 [DOID:0110477] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the MYO7A gene on chromosome 11q13.

synonyms:
600060,
autosomal recessive deafness 2,
OMIM:600060,
ICD10CM:H90.3,
DFNB2

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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