Status: current, Primitive. Date: 30-Apr 2018. Module: SNOMED Clinical Terms Australian extension
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2313551000168114 | Mutation of MYC associated factor X gene inherited from father (finding) | en | Fully specified name | Active | Initial character case insensitive | SNOMED Clinical Terms Australian extension |
2313561000168111 | Paternally inherited MAX gene mutation | en | Synonym | Active | Initial character case insensitive | SNOMED Clinical Terms Australian extension |
2313571000168117 | Mutation of MYC associated factor X gene inherited from father | en | Synonym | Active | Initial character case insensitive | SNOMED Clinical Terms Australian extension |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Paternally inherited MAX gene mutation | Is a | Genetic mutation | true | Inferred relationship | Some | ||
Paternally inherited MAX gene mutation | Interprets | Genetic test | false | Inferred relationship | Some | ||
Paternally inherited MAX gene mutation | Interprets | Genetic test | true | Inferred relationship | Some | 1946671443 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set