OBO ID: DOID:0110546
Term Name: autosomal dominant nonsyndromic deafness 15 Search Ontology:
Synonyms:
  • autosomal dominant deafness 15
  • DFNA15
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
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
POU4F3 Deafness, autosomal dominant 15 602459
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None