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.

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↑ Brugada syndrome (10)

Including sub-types (32) Tagged with Brugada syndrome 5 (0)

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