Search Ontology:
Human Disease

autosomal recessive nonsyndromic deafness 39

Term ID
DOID:0110497
Synonyms
  • autosomal recessive deafness 39
  • DFNB39
Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21. https://www.ncbi.nlm.nih.gov/pubmed/19576567
References
Ontology
Human Disease   ( DOID:0110497 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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.