Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder) | | Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | | Arthropathy camptodactyly syndrome CACP (camptodactyly, arthropathy, coxa-vara, pericarditis) syndrome CACP syndrome Jacobs syndrome Pericarditis, arthropathy, camptodactyly syndrome
| | A rare genetic rheumatologic disease with characteristics of congenital or early-onset camptodactyly and symmetrical, polyarticular, non-inflammatory, large joint arthropathy with synovial hyperplasia, as well as progressive coxa vara deformity and, occasionally, non-inflammatory pericarditis. There is evidence the disease can be caused by homozygous mutation in the proteoglycan-4 gene (PRG4) on chromosome 1q31. | | syndroom van camptodactylie, artropathie, coxa vara en pericarditis | | CACP-syndroom
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| Id | 771187008 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | Target | Q87.5 | Rule | TRUE | Advice | ALWAYS Q87.5 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | Correlation | SNOMED CT source code to target map code correlation not specified |
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