Status: current, Primitive. Date: 30-Apr 2018. Module: SNOMED Clinical Terms Australian extension
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2313521000168118 | Mutation of MYC associated factor X gene inherited from mother (finding) | en | Fully specified name | Active | Initial character case insensitive | SNOMED Clinical Terms Australian extension |
2313531000168115 | Maternally inherited MAX gene mutation | en | Synonym | Active | Initial character case insensitive | SNOMED Clinical Terms Australian extension |
2313541000168112 | Mutation of MYC associated factor X gene inherited from mother | en | Synonym | Active | Initial character case insensitive | SNOMED Clinical Terms Australian extension |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Maternally inherited MAX gene mutation | Is a | Genetic mutation | true | Inferred relationship | Some | ||
Maternally inherited MAX gene mutation | Interprets | Genetic test | false | Inferred relationship | Some | ||
Maternally inherited MAX gene mutation | Interprets | Genetic test | true | Inferred relationship | Some | 1279845867 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set