Brugada syndrome 5

MONDO:0013015

Any Brugada syndrome in which the cause of the disease is a mutation in the SCN1B gene.

Also known as: BRGDA5, Brugada syndrome 5, Brugada syndrome caused by mutation in SCN1B, Brugada syndrome type 5, SCN1B Brugada syndrome, Cardiac conduction defect, nonspecific

32 clinical trials for this condition and its sub-types, 0 tagged with Brugada syndrome 5 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by