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DO Term : autosomal recessive nonsyndromic deafness 31 [DOID:0110490] 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 WHRN gene on chromosome 9q32.
  • synonyms:
  • OMIM:607084,
  • 607084,
  • autosomal recessive deafness 31,
  • DFNB31,
  • 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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