Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2922800017 | Long QT syndrome with genetic marker (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
2922801018 | Long QT syndrome with genetic marker | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3620091000052117 | långt QT-syndrom med genetisk markör | sv | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
långt QT-syndrom med genetisk markör | Is a | Congenital long QT syndrome (disorder) | false | Inferred relationship | Some | ||
långt QT-syndrom med genetisk markör | Occurrence | Congenital | false | Inferred relationship | Some | 2 | |
långt QT-syndrom med genetisk markör | Finding site | Cardiac conducting system structure | false | Inferred relationship | Some | ||
långt QT-syndrom med genetisk markör | Finding site | Heart structure | false | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Romano-Ward syndrome | Is a | False | långt QT-syndrom med genetisk markör | Inferred relationship | Some | |
Jervell and Lange-Nielsen syndrome | Is a | False | långt QT-syndrom med genetisk markör | Inferred relationship | Some | |
Andersen Tawil syndrome (disorder) | Is a | False | långt QT-syndrom med genetisk markör | Inferred relationship | Some | |
Timothy syndrome type 1 (disorder) | Is a | False | långt QT-syndrom med genetisk markör | Inferred relationship | Some | |
Timothy syndrome type 2 (disorder) | Is a | False | långt QT-syndrom med genetisk markör | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)