Usher syndrome type 1C (Q32143522)

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Usher syndrome type 1 that has material basis in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15
  • Usher syndrome type I Acadian variety
  • USH1C
  • Usher syndrome type IC
  • Usher Syndrome, Type I, Acadian Variety
  • USHER SYNDROME, TYPE IC
  • Usher syndrome, Acadian variety
  • Usher syndrome, type 1C
  • USHER SYNDROME, TYPE IC; USH1C
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Language Label Description Also known as
English
Usher syndrome type 1C
Usher syndrome type 1 that has material basis in homozygous or compound heterozygous mutation in the USH1C gene on chromosome 11p15
  • Usher syndrome type I Acadian variety
  • USH1C
  • Usher syndrome type IC
  • Usher Syndrome, Type I, Acadian Variety
  • USHER SYNDROME, TYPE IC
  • Usher syndrome, Acadian variety
  • Usher syndrome, type 1C
  • USHER SYNDROME, TYPE IC; USH1C

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