SCN5A-related cardiac rhythm disorder

MONDO:1010181

A heterogeneous collection of cardiac rhythm disorders caused by genetic variations in the SCN5A gene with autosomal dominant inheritance. Affected individuals are commonly reported to have unremarkable cardiac morphology and at least one cardiac rhythm phenotype that includes, but is not limited to, atrial fibrillation, sick sinus syndrome, progressive cardiac conduction disease, ventricular fibrillation, long QT syndrome, and Brugada syndrome.

Also known as: SCN5A-related cardiac rhythm disorder

77 clinical trials for this condition and its sub-types, 0 tagged with SCN5A-related cardiac rhythm disorder itself.

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↑ Cardiogenetic rhythm disorder (68)

Sub-types of SCN5A-related cardiac rhythm disorder

Ventricular fibrillation, paroxysmal familial, type 1 25 trials
Progressive familial heart block, type 1A 19 trials
Long QT syndrome 3 6 trials
Brugada syndrome 1 0 trials
Atrial fibrillation, familial, 10 0 trials
Sick sinus syndrome 1 0 trials

Including sub-types (77) Tagged with SCN5A-related cardiac rhythm disorder (0)

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