OBO ID: DOID:0110570
Term Name: autosomal dominant nonsyndromic deafness 47 Search Ontology:
Synonyms:
  • autosomal dominant deafness 47
  • DFNA47
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 9p22-p21. https://www.ncbi.nlm.nih.gov/pubmed/12634859
References:
Ontology: Human Disease   ( DOID:0110570 )
Relationships
is a type of:
OTHER autosomal dominant nonsyndromic deafness 47 PAGES
GENES INVOLVED No data available
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.