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GENATLAS PHENOTYPE
last update : 25-02-2016
Symbol DFNB68
Location 19p13.2
Name neurosensory deafness 68
Corresponding gene S1PR2
Main clinical features
  • nonsyndromic sensorineural hearing loss, congenital profound hearing impairment
  • Genetic determination autosomal recessive
    Function/system disorder ear
    Type disease
    Remark(s)