Brugada syndrome 1

MONDO:0011001

Any Brugada syndrome in which the cause of the disease is a mutation in the SCN5A gene.

Also known as: BRGDA1, Brugada syndrome 1, Brugada syndrome caused by mutation in SCN5A, Brugada syndrome type 1, SCN5A Brugada syndrome, Cardiac conduction defect, nonspecific, right bundle branch block, St segment elevation, and sudden death syndrome, sudden unexplained nocturnal death syndrome

32 clinical trials for this condition and its sub-types, 0 tagged with Brugada syndrome 1 itself.

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Including sub-types (32) Tagged with Brugada syndrome 1 (0)

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