Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2790283013 | Prothrombin G20210A mutation | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Prothrombin G20210A mutation (disorder) | Is a | Hereditary thrombophilia (disorder) | true | Inferred relationship | Some | ||
| Prothrombin G20210A mutation (disorder) | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
| Prothrombin G20210A mutation (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Prothrombin G20210A mutation (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Homozygous prothrombin G20210A mutation (disorder) | Is a | True | Prothrombin G20210A mutation (disorder) | Inferred relationship | Some | |
| Heterozygous prothrombin G20210A mutation (disorder) | Is a | True | Prothrombin G20210A mutation (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR