Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3037563018 | Factor 5 Leiden mutation | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 450270016 | Factor V Leiden mutation | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 703570019 | Factor V Leiden mutation (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Factor V Leiden mutation | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Factor V Leiden mutation | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Factor V Leiden mutation | Is a | Thrombophilia | false | Inferred relationship | Some | ||
| Factor V Leiden mutation | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Factor V Leiden mutation | Has definitional manifestation | Haemostatic system finding | false | Inferred relationship | Some | ||
| Factor V Leiden mutation | Is a | Hereditary thrombophilia | true | Inferred relationship | Some | ||
| Factor V Leiden mutation | Finding site | Entire haematological system | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Homozygous Factor V Leiden mutation | Is a | True | Factor V Leiden mutation | Inferred relationship | Some | |
| Heterozygous Factor V Leiden mutation | Is a | True | Factor V Leiden mutation | Inferred relationship | Some | |
| Resistance to activated protein C due to Factor V Leiden | Due to | True | Factor V Leiden mutation | Inferred relationship | Some | 1 |
| Factor V Leiden screening test | Has focus | True | Factor V Leiden mutation | Inferred relationship | Some | 2 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR