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Brugada syndrome 4

Disease Summary
Associated Targets (2)
Tbio

2


GARD Rare
Mondo Description Any Brugada syndrome in which the cause of the disease is a mutation in the CACNB2 gene.
Uniprot Description A heart disease characterized by the association of Brugada syndrome with shortened QT intervals. Brugada syndrome is a tachyarrhythmia characterized by right bundle branch block and ST segment elevation on an electrocardiogram (ECG). It can cause the ventricles to beat so fast that the blood is prevented from circulating efficiently in the body. When this situation occurs, the individual will faint and may die in a few minutes if the heart is not reset.
Mondo Term and Equivalent IDs
MONDO:0012743:  Brugada syndrome 4
GARD:0010362: 
MESH:C567508: 
UMLS:C2678477: