Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 106718015 | Genetic variation | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 803561018 | Genetic variation (finding) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Genetic variation | Is a | Genetic finding | true | Inferred relationship | Some | ||
| Genetic variation | Interprets | Laboratory test | false | Inferred relationship | Some | ||
| Genetic variation | Finding method | Procedure | false | Inferred relationship | Some | ||
| Genetic variation | Interprets | Genetic test | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR