camptodactyly-arthropathy-coxa vara-pericarditis syndrome (Q5028560)
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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
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | camptodactyly-arthropathy-coxa vara-pericarditis syndrome |
autosomal recessive genetic condition |
|
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