| Id | Description | Lang | Type | Status | Case? | Module | 
| 3704819016 | Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 3704820010 | Arthropathy camptodactyly syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 3704821014 | Pericarditis, arthropathy, camptodactyly syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module | 
| 3704822019 | Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module | 
| 3704823012 | Jacobs syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module | 
| 3704824018 | CACP (camptodactyly, arthropathy, coxa-vara, pericarditis) syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module | 
| 3704825017 | CACP syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module | 
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values | 
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Is a | Flexion deformity of finger | false | Inferred relationship | Existential restriction modifier |  |  | 
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Finding site | Proximal interphalangeal joint of finger structure | true | Inferred relationship | Existential restriction modifier | 1 |  | 
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Is a | Polyarthropathy | true | Inferred relationship | Existential restriction modifier |  |  | 
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Associated morphology | Flexion deformity | false | Inferred relationship | Existential restriction modifier | 1 |  | 
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Existential restriction modifier |  |  | 
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier |  |  | 
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Finding site | Joint structure of multiple body sites | true | Inferred relationship | Existential restriction modifier | 2 |  | 
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Associated morphology | Fixed flexion deformity | true | Inferred relationship | Existential restriction modifier | 1 |  | 
| Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Is a | Fixed flexion deformity finger | true | Inferred relationship | Existential restriction modifier |  |  |