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ENCamptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome (CACP)
Alias:
Jacobs Syndrome
Pericarditis-Arthropathy-Camptodactyly Syndrome
Arthropathy-Camptodactyly Syndrome
Cacp Syndrome
Camptodactyly-Arthropathy-Coxa-Vara-Pericarditis Syndrome
Camptodactyly-Arthropathy-Pericarditis Syndrome
Pac Syndrome
Cap Syndrome
Cacp
Hypertrophic Synovitis, Congenital Familial
Fibrosing Serositis, Familial
Congenital Familial Hypertrophic Synovitis
Familial Fibrosing Serositis
Cdags Syndrome
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Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome, also known as jacobs syndrome, is related to coxa vara and pericarditis. An important gene associated with Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome is PRG4 (Proteoglycan 4), and among its related pathways/superpathways are Cardiac conduction and Striated muscle contraction pathway. Affiliated tissues include bone and heart, and related phenotypes are coxa vara and camptodactyly of finger
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MALACARDS
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