Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3433007011 | Carrier of high risk cancer mutation gene (finding) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3433008018 | Carrier of high risk cancer mutation gene | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Carrier of high risk cancer mutation gene | Associated morphology | Congenital anomaly | false | Inferred relationship | Some | ||
| Carrier of high risk cancer mutation gene | Is a | Genetic disorder carrier | true | Inferred relationship | Some | ||
| Carrier of high risk cancer mutation gene | Interprets | General clinical state | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Australian dialect reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set
FHIR