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418818005: Brugada syndrome (disorder)


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


0 descendants.

Expanded Value Set


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

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