Status: current, Primitive. Date: 31-Jan 2009. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2789930019 | Prothrombin G20210A mutation (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 2790283013 | Prothrombin G20210A mutation | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Prothrombin G20210A mutation | Interprets | Haemostatic function | true | Inferred relationship | Some | 1 | |
| Prothrombin G20210A mutation | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Prothrombin G20210A mutation | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Prothrombin G20210A mutation | Is a | Hereditary thrombophilia | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Homozygous prothrombin G20210A mutation | Is a | True | Prothrombin G20210A mutation | Inferred relationship | Some | |
| Heterozygous prothrombin G20210A mutation | Is a | True | Prothrombin G20210A mutation | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR