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References OMIM Gene GeneReviews HGMD HGNC
last update : 28-11-2012
Symbol DFNB18B
Location 11p15.1
Name deafness, autosomal recessive 18B
Corresponding gene OTOG
Main clinical features
  • moderate nonsyndromic hearing loss
  • nonsyndromic deafness, who all had flat to shallow U-shaped audiograms
  • prelingual onset of the hearing impairment, and delayed motor development, suggestive of vestibular problems at a young age
  • Genetic determination autosomal recessive
    autosomal dominant
    Function/system disorder ear
    Type disease