Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 179087019 | Familial disease | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 635166017 | Familial disease (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial disease | Is a | Disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial isolated clinodactyly of finger | Is a | True | Familial disease | Inferred relationship | Some | |
| Familial myoclonus of cerebral cortex | Is a | True | Familial disease | Inferred relationship | Some | |
| Retinal arterial macroaneurysm with supravalvular pulmonic stenosis | Is a | True | Familial disease | Inferred relationship | Some | |
| Familial isolated trichomegaly | Is a | True | Familial disease | Inferred relationship | Some | |
| Familial thoracic aortic aneurysm and aortic dissection | Is a | True | Familial disease | Inferred relationship | Some | |
| Familial lambdoid synostosis | Is a | False | Familial disease | Inferred relationship | Some | |
| Familial multiple lipomatosis | Is a | True | Familial disease | Inferred relationship | Some | |
| Familial supernumerary nipple | Is a | True | Familial disease | Inferred relationship | Some | |
| Familial haemophagocytic lymphohistiocytosis | Is a | True | Familial disease | Inferred relationship | Some |
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Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR