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Human Disease

autosomal dominant nonsyndromic deafness 6

Term ID
DOID:0110584
Synonyms
  • autosomal dominant deafness 14
  • autosomal dominant deafness 38
  • autosomal dominant deafness 6
  • DFNA14
  • DFNA38
  • DFNA6
  • DFNA6/14/38
Definition
An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and low frequency progressive hearing loss and has_material_basis_in mutation in the WFS1 gene on chromosome 4p16. (2)
References
Ontology
Human Disease   ( DOID:0110584 )
Relationships
is a type of
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Genes Involved
Zebrafish Models