Long QT syndrome 3

MONDO:0011377

An autosomal dominant condition caused by mutation(s) in the SCN5A gene, encoding sodium channel protein type 5 subunit alpha. It is characterized by a prolonged QT interval that may result in torsade de pointes, ventricular fibrillation and/or sudden cardiac death.

Also known as: LQT3, SCN5A long QT syndrome, long QT syndrome 3, long QT syndrome caused by mutation in SCN5A, long QT syndrome type 3, long QT syndrome 2/3, digenic, long QT syndrome 3, acquired, susceptibility to, long QT syndrome 3/6, digenic

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