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DO Term : autosomal recessive nonsyndromic deafness 26 [DOID:0110484] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An autosomal recessive nonsyndromic deafness that has_material_basis_in homozygous mutation in the GAB1 gene on chromosome 4q31.
  • synonyms:
  • autosomal recessive deafness 26,
  • 605428,
  • DFNB26,
  • OMIM:605428,
  • ICD10CM:H90.3
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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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