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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
  • non syndromic
  • one form of the MYH2A syndrome, with cochleosaccular degeneration
  • 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)