Usher syndrome type 2C (Q32143643)

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Usher syndrome type 2 that has material basis in homozygous or compound heterozygous mutation in the ADGRV1 gene on chromosome 5q14
  • USH2C
  • Usher syndrome type IIC
  • Usher syndrome, type 2C
  • USHER SYNDROME, TYPE IIC
  • USHER SYNDROME, TYPE IIC; USH2C
  • Usher Syndrome, Type Iib, Formerly
  • Usher Syndrome, Type Iib
  • Usher Syndrome, Type Iic, Gpr98/Pdzd7, Digenic
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English
Usher syndrome type 2C
Usher syndrome type 2 that has material basis in homozygous or compound heterozygous mutation in the ADGRV1 gene on chromosome 5q14
  • USH2C
  • Usher syndrome type IIC
  • Usher syndrome, type 2C
  • USHER SYNDROME, TYPE IIC
  • USHER SYNDROME, TYPE IIC; USH2C
  • Usher Syndrome, Type Iib, Formerly
  • Usher Syndrome, Type Iib
  • Usher Syndrome, Type Iic, Gpr98/Pdzd7, Digenic

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