OBO ID: DOID:0110584
Term Name: autosomal dominant nonsyndromic deafness 6 Search Ontology:
Synonyms:
  • autosomal dominant deafness 14
  • autosomal dominant deafness 38
  • autosomal dominant deafness 6
  • DFNA14
  • DFNA38
  • DFNA6
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:
OTHER autosomal dominant nonsyndromic deafness 6 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WFS1 Deafness, autosomal dominant 6/14/38 600965
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.