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Brugada syndrome

Disease Summary
Associated Targets (27)
Tbio

17

Tclin

9

Tchem

1


GARD Rare
Mondo Description A genetically heterogeneous condition characterized by complete or incomplete right bundle branch block accompanied by ST elevation in leads V1-V3. There is a high incidence of ventricular arrhythmia that may result in sudden death.
Disease Ontology Description A heart conduction disease that is characterized by abnormal electrocardiogram (ECG) findings and an increased risk of sudden cardiac death.
Mondo Term and Equivalent IDs
MONDO:0015263:  Brugada syndrome
GARD:0001030: 
MESH:D053840: 
NCIT:C142891: 
OMIMPS:601144: 
Orphanet:130: 
SCTID:418818005: 
UMLS:C1142166: