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418818005: Brugada syndrome (disorder)


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


0 descendants.

Expanded Value Set


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

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