About: Brugada Syndrome Ventricular Arrythmia     Goto   Sponge   Distinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz:8890 associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Brugada Syndrome Ventricular Arrythmia
rdfs:subClassOf
Concept_In_Subset
Semantic_Type
  • Finding
Preferred_Name
  • Brugada Syndrome Ventricular Arrythmia
UMLS_CUI
  • C1142166
Contributing_Source
  • CDISC
ALT_DEFINITION
  • Polymorphic ventricular tachycardia in the absence of structural heart disease, associated with a baseline ECG pattern during sinus rhythm showing right bundle branch block with ST segment elevation in leads V1 through V3. It can also be characterized by documentation of ECG patterns associated with Brugada Syndrome, some of which may be unmasked when provoked with drugs. The most common genetic mutations identified for Brugada syndrome are in the sodium channel gene SCN5A.CDISC
Legacy_Concept_Name
  • Brugada_Syndrome
FULL_SYN
  • BRUGADA SYNDROMEPTCDISCSDTM-SDTHSDTP
  • Brugada Syndrome Ventricular ArrythmiaPTNCI
  • VENTRICULAR ARRHYTHMIA ASSOCIATED WITH BRUGADA SYNDROMEPTCDISCSDTM-EGSTRESC
  • Ventricular arrhythmia associated with Brugada syndromeSYCDISC
DEFINITION
  • An electrocardiographic finding of a pattern of right bundle branch block and ST-segment elevation within electrocardiogram leads V1-V3. This pattern emerges as a result of a defect in ion channel genes, resulting in atypical electrophysiological activity in the right ventricle and a propensity for malignant tachyarrhythmias.NCI
code
  • C71059
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