Home Page |
References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 30/03/2006 |
Symbol | DFNA17 |
Location | 22q12.3 |
HGNC id | 2790 |
Name | neurosensory deafness 17 |
Corresponding gene | MYH9 |
Main clinical features |
|
Genetic determination | autosomal dominant |
Related entries | including rare cases of macrothrombocytopenia and progressive sensorineural hearing loss (OMIM600208) |
Function/system disorder | ear |
Type | disease |
Gene product |
Name | myosin heavy chain 9 |
Remark(s) |