Status: current, Defined. Date: 31-Jan 2010. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2834302013 | Congenital long QT syndrome (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| 2837534014 | Congenital long QT syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 2837535010 | Inherited long QT syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3901309016 | Familial long QT syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Andersen Tawil syndrome | Is a | True | Congenital long QT syndrome | Inferred relationship | Some | |
| Timothy syndrome type 2 | Is a | True | Congenital long QT syndrome | Inferred relationship | Some | |
| Timothy syndrome type 1 | Is a | True | Congenital long QT syndrome | Inferred relationship | Some | |
| Long QT syndrome type 9 | Is a | True | Congenital long QT syndrome | Inferred relationship | Some | |
| Long QT syndrome type 6 | Is a | True | Congenital long QT syndrome | Inferred relationship | Some | |
| Romano-Ward syndrome | Is a | True | Congenital long QT syndrome | Inferred relationship | Some | |
| Jervell and Lange-Nielsen syndrome | Is a | True | Congenital long QT syndrome | Inferred relationship | Some | |
| Long QT syndrome with genetic marker | Is a | False | Congenital long QT syndrome | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set