autosomal dominant nonsyndromic deafness 12 (Q28024671)

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autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and has material basis in mutation in the TECTA gene on chromosome 11q23
  • DFNA12
  • DFNA8
  • autosomal dominant deafness 12
  • autosomal dominant deafness 8
  • autosomal dominant nonsyndromic deafness type 12
  • Deafness, Autosomal Dominant type 12
  • DEAFNESS, AUTOSOMAL DOMINANT 12; DFNA12
  • DEAFNESS, AUTOSOMAL DOMINANT 12
  • Deafness, Autosomal Dominant 8
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English
autosomal dominant nonsyndromic deafness 12
autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and has material basis in mutation in the TECTA gene on chromosome 11q23
  • DFNA12
  • DFNA8
  • autosomal dominant deafness 12
  • autosomal dominant deafness 8
  • autosomal dominant nonsyndromic deafness type 12
  • Deafness, Autosomal Dominant type 12
  • DEAFNESS, AUTOSOMAL DOMINANT 12; DFNA12
  • DEAFNESS, AUTOSOMAL DOMINANT 12
  • Deafness, Autosomal Dominant 8

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