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DO Term : autosomal dominant nonsyndromic deafness 2A [DOID:0110558] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An autosomal dominant nonsyndromic deafness that is characterized by high frequency progressive hearing loss and has_material_basis_in mutation in the KCNQ4 gene on chromosome 1p34.2.
  • synonyms:
  • OMIM:600101,
  • 600101,
  • autosomal dominant deafness 2A,
  • DFNA2A,
  • 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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