All diseases

OMIM ID
208250
OMIM term:
CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME; CACP
Alternative terms:
ARTHROPATHY-CAMPTODACTYLY SYNDROME
HYPERTROPHIC SYNOVITIS, CONGENITAL FAMILIAL
JACOBS SYNDROME
FIBROSING SEROSITIS, FAMILIAL
PERICARDITIS-ARTHROPATHY-CAMPTODACTYLY SYNDROME
PAC SYNDROME
CAMPTODACTYLY-ARTHROPATHY-PERICARDITIS SYNDROME
CAP SYNDROME
(∗) Location:
1q31.1  
(†) Associated OMIM genes:
PRG4  
(‡) Associated MGI genes:
Prg4  

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