OBO ID: DOID:0110593
Term Name: autosomal dominant nonsyndromic deafness 9 Search Ontology:
Synonyms:
  • autosomal dominant deafness 9
  • DFNA9
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade with high frequency progressive hearing loss and has_material_basis_in mutation in the COCH gene on chromosome 14q12. https://www.ncbi.nlm.nih.gov/pubmed/9806553
References:
Ontology: Human Disease   ( DOID:0110593 )
Relationships
is a type of:
OTHER autosomal dominant nonsyndromic deafness 9 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
COCH Deafness, autosomal dominant 9 601369
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.