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418818005: Brugada syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case sensitive (core metadata concept) SNOMED CT core
2576883015 Brugada syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Brugada syndrome (disorder) Is a Conduction disorder of the heart false Inferred relationship Some
Brugada syndrome (disorder) Finding site Cardiac conducting system structure false Inferred relationship Some
Brugada syndrome (disorder) Finding site Heart structure false Inferred relationship Some 1
Brugada syndrome (disorder) Is a Cardiac arrhythmia associated with genetic disorder (disorder) true Inferred relationship Some
Brugada syndrome (disorder) Is a Cardiac channelopathy true Inferred relationship Some
Brugada syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Brugada syndrome (disorder) Is a Cardiovascular system hereditary disorder true Inferred relationship Some
Brugada syndrome (disorder) Finding site Cardiac conducting system structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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