Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2006. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2573583018 | Brugada syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
2576883015 | Brugada syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Brugada syndrome | Is a | Conduction disorder of the heart | false | Inferred relationship | Existential restriction modifier | ||
Brugada syndrome | Finding site | Cardiac conducting system structure | false | Inferred relationship | Existential restriction modifier | ||
Brugada syndrome | Finding site | Heart structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Brugada syndrome | Is a | Cardiac arrhythmia associated with genetic disorder | true | Inferred relationship | Existential restriction modifier | ||
Brugada syndrome | Is a | Cardiac channelopathy | true | Inferred relationship | Existential restriction modifier | ||
Brugada syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Brugada syndrome | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets