Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2973631016 | Short QT syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2973635013 | Short QT syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3792916010 | Familial short QT syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3792917018 | Genetic short QT syndrome | 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 |
| Short QT syndrome (disorder) | Is a | A disorder that affects the myocardial ion channels, altering the electrical properties of the heart and changing the ECG and/or predisposing the subject to pro-arrhythmic events. | true | Inferred relationship | Some | ||
| Short QT syndrome (disorder) | Finding site | Heart structure | false | Inferred relationship | Some | 1 | |
| Short QT syndrome (disorder) | Is a | A disorder in which there is abnormal electrical activity in the heart associated with a genetic disorder. | true | Inferred relationship | Some | ||
| Short QT syndrome (disorder) | Finding site | Cardiac conducting system structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Genetic short QT syndrome | Is a | False | Short QT syndrome (disorder) | Inferred relationship | Some |
This concept is not in any reference sets
FHIR