(Q5028560)

(Redirected from Q30989065)
English

camptodactyly-arthropathy-coxa vara-pericarditis syndrome

autosomal recessive genetic condition

  • camptodactyly-arthropathy-pericarditis syndrome
  • CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME
  • CACP syndrome
  • familial fibrosing serositis
  • Camptodactyly arthropathy pericarditis syndrome
  • CACP
  • PAC syndrome
  • Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
  • arthropathy-camptodactyly syndrome
  • Pericarditis arthropathy camptodactyly syndrome
  • pericarditis-arthropathy-camptodactyly syndrome
  • Camptodactyly arthropathy coxa vara pericarditis syndrome
  • Arthropathy camptodactyly syndrome
  • CAP syndrome
  • congenital familial hypertrophic synovitis
  • Jacobs syndrome
  • Fibrosing serositis, familial
  • CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME; CACP
  • Hypertrophic Synovitis, Congenital Familial

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