Status: current, Defined. Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2789416017 | Hereditary thrombophilia (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
2794141016 | Hereditary thrombophilia | en | Synonym | Active | Case insensitive | SNOMED CT core |
2794142011 | Hereditary hypercoagulable disorder | en | Synonym | Active | Case insensitive | SNOMED CT core |
2871986010 | Primary thrombophilia | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary thrombophilia | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
Hereditary thrombophilia | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
Hereditary thrombophilia | Is a | Hereditary disease | true | Inferred relationship | Some | ||
Hereditary thrombophilia | Is a | Thrombophilia | true | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set