All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00865 CACP camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) 208250 AR 12 11 PRG4 - congenital or early-onset camptodactyly and noninflammatory arthropathy with synovial hyperplasia, in some patients progressive coxa vara deformity and/or noninflammatory pericardial or pleural effusions
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