Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3704819016 | Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3704820010 | Arthropathy camptodactyly syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3704821014 | Pericarditis, arthropathy, camptodactyly syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3704822019 | Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3704823012 | Jacobs syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3704824018 | CACP (camptodactyly, arthropathy, coxa-vara, pericarditis) syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3704825017 | CACP syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3704829011 | 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. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Finding site | Joint structure of multiple body sites | true | Inferred relationship | Some | 2 | |
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Associated morphology | Fixed flexion deformity | true | Inferred relationship | Some | 1 | |
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Is a | Fixed flexion deformity finger | true | Inferred relationship | Some | ||
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Is a | Flexion deformity of finger | false | Inferred relationship | Some | ||
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Finding site | Proximal interphalangeal joint of finger structure | true | Inferred relationship | Some | 1 | |
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Is a | Polyarthropathy | true | Inferred relationship | Some | ||
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Associated morphology | Flexion deformity | false | Inferred relationship | Some | 1 | |
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Is a | Hereditary disorder of musculoskeletal system | true | Inferred relationship | Some | ||
Camptodactyly, arthropathy, coxa-vara, pericarditis syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set