(Q32147433)

English

nephronophthisis 12

nephronophthisis that has material basis in homozygous or compound heterozygous mutation in the TTC21B gene on chromosome 2q24

  • NPHP12
  • NEPHRONOPHTHISIS 12; NPHP12
  • Nephronophthisis type 12
  • Joubert Syndrome 11
  • NEPHRONOPHTHISIS 12

Statements

Identifiers

 
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