OBO ID: DOID:0110546 |
Term Name: | autosomal dominant nonsyndromic deafness 15 | Search Ontology: | |
---|---|---|---|
Synonyms: |
|
||
Definition: | An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the POU4F3 gene on chromosome 5q32. https://www.ncbi.nlm.nih.gov/pubmed/9506947 | ||
References: |
|
||
Ontology: | Human Disease ( DOID:0110546 ) |
OTHER autosomal dominant nonsyndromic deafness 15 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
Your Input Welcome
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.