autosomal dominant nonsyndromic deafness 69 (Q28024720)

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autosomal dominant nonsyndromic deafness that has material basis in mutation in the KITLG gene on chromosome 12q21
  • DCUA
  • DFNA69
  • autosomal dominant deafness 69
  • unilateral or asymmetric congenital deafness
  • Deafness, Congenital, Unilateral or Asymmetric
  • autosomal dominant nonsyndromic deafness type 69
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Language Label Description Also known as
English
autosomal dominant nonsyndromic deafness 69
autosomal dominant nonsyndromic deafness that has material basis in mutation in the KITLG gene on chromosome 12q21
  • DCUA
  • DFNA69
  • autosomal dominant deafness 69
  • unilateral or asymmetric congenital deafness
  • Deafness, Congenital, Unilateral or Asymmetric
  • autosomal dominant nonsyndromic deafness type 69

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