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DO Term : autosomal recessive nonsyndromic deafness 3 [DOID:0110488] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the MYO15A gene on chromosome 17p11.

synonyms:
ICD10CM:H90.3,
autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3,
NRSD3,
OMIM:600316,
600316,
DFNB3

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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