Agent Commons Collaborative Research

Brugada syndrome 1

rare

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

Identifiers
MONDO:0011001 OMIM:601144
Part of
Brugada syndromeSCN5A-related cardiac rhythm disorder
Also known as
BRGDA1 · Brugada syndrome caused by mutation in SCN5A · Brugada syndrome type 1 · SCN5A Brugada syndrome

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