Status: current, Primitive. Date: 30-Apr 2018. Module: SNOMED Clinical Terms Australian extension
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2313491000168115 | Mutation of succinate dehydrogenase complex assembly factor 2 gene inherited from father (finding) | en | Fully specified name | Active | Case insensitive | SNOMED Clinical Terms Australian extension |
| 2313501000168110 | Paternally inherited SDHAF2 gene mutation | en | Synonym | Active | Initial character case insensitive | SNOMED Clinical Terms Australian extension |
| 2313511000168113 | Mutation of succinate dehydrogenase complex assembly factor 2 gene inherited from father | en | Synonym | Active | Case insensitive | SNOMED Clinical Terms Australian extension |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Paternally inherited SDHAF2 gene mutation | Is a | Genetic mutation | true | Inferred relationship | Some | ||
| Paternally inherited SDHAF2 gene mutation | Interprets | Genetic test | false | Inferred relationship | Some | ||
| Paternally inherited SDHAF2 gene mutation | Interprets | Genetic test | true | Inferred relationship | Some | 633075990 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR