OBO ID: DOID:0110548
Term Name: autosomal dominant nonsyndromic deafness 17 Search Ontology:
Synonyms:
  • autosomal dominant deafness 17
  • DFNA17
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 MYH9 gene on chromosome 22q12.https://www.ncbi.nlm.nih.gov/pubmed/11023810
References:
Ontology: Human Disease   (DOID:0110548)
Relationships
is a type of:
OTHER autosomal dominant nonsyndromic deafness 17 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MYH9 Deafness, autosomal dominant 17 603622
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None