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DO Term : autosomal recessive nonsyndromic deafness 8 [DOID:0110527] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TMPRSS3 gene on chromosome 21q22.

synonyms:
DFNB10,
OMIM:601072,
childhood-onset neurosensory autosomal recessive deafness 8,
autosomal recessive deafness 8,
neurosensory nonsyndromic recessive deafness 8,
autosomal recessive deafness 10,
NRSD8,
ICD10CM:H90.3,
DFNB8,
601072

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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