(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
Statements
2 references
1 reference
1 reference
1 reference
1 reference
4 references
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference