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 |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Long QT syndrome with genetic marker (disorder) | est un(e) (attribut) | Congenital long QT syndrome (disorder) | false | Inferred relationship | Some | ||
| Long QT syndrome with genetic marker (disorder) | survenue (attribut) | congénital | false | Inferred relationship | Some | 2 | |
| Long QT syndrome with genetic marker (disorder) | localisation d'une constatation (attribut) | structure du système de conduction cardiaque | false | Inferred relationship | Some | ||
| Long QT syndrome with genetic marker (disorder) | localisation d'une constatation (attribut) | cœur | false | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Romano-Ward syndrome | est un(e) (attribut) | False | Long QT syndrome with genetic marker (disorder) | Inferred relationship | Some | |
| Jervell and Lange-Nielsen syndrome | est un(e) (attribut) | False | Long QT syndrome with genetic marker (disorder) | Inferred relationship | Some | |
| Andersen Tawil syndrome (disorder) | est un(e) (attribut) | False | Long QT syndrome with genetic marker (disorder) | Inferred relationship | Some | |
| Timothy syndrome type 1 (disorder) | est un(e) (attribut) | False | Long QT syndrome with genetic marker (disorder) | Inferred relationship | Some | |
| Timothy syndrome type 2 (disorder) | est un(e) (attribut) | False | Long QT syndrome with genetic marker (disorder) | Inferred relationship | Some |
Reference Sets
Concept inactivation indicator reference set
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)
FHIR