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References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 21-09-2011
Symbol DFNA50
Location 7q32.1-q32.2
HGNC id 18819
Name neurosensory deafness 50
Corresponding gene MIR96
Main clinical features
  • postlingual, progressive, nonsyndromic all-frequency hearing loss
  • hearing loss was initially mild, affecting all frequencies, and progressed to severe or profound in the seventh decade
  • Genetic determination autosomal dominant
    Function/system disorder ear
    Type disease
    Remark(s)