Status: current, Primitive. Date: 31-Jan 2006. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2573583018 | Brugada syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
2576883015 | Brugada syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
2973642013 | Clinical manifestations of cardiac syncope, ventricular tachycardia, ventricular fibrillation, or sudden death in conjunction with a genetic mutation associated with Brugada Syndrome and/or a Brugada pattern ECG (spontaneous or provoked). | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Brugada syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Brugada syndrome | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
Brugada syndrome | Is a | Conduction disorder of the heart | false | Inferred relationship | Some | ||
Brugada syndrome | Finding site | Cardiac conducting system structure | false | Inferred relationship | Some | ||
Brugada syndrome | Finding site | Structure of heart | true | Inferred relationship | Some | 1 | |
Brugada syndrome | Is a | Cardiac arrhythmia associated with genetic disorder | true | Inferred relationship | Some | ||
Brugada syndrome | Is a | Cardiac channelopathy | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set