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GENATLAS PHENOTYPE
last update : 04-06-2010
Symbol DFNB91
Location 6p25
Name neurosensory deafness 91
Corresponding gene SERPINB6
Main clinical features
  • congenital profound sensori-neural hearing loss
  • Genetic determination autosomal recessive
    Prevalence 1.7 p100 of all DFNB (PMID: 21117948)
    Function/system disorder ear
    Type disease
    Remark(s)