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Short QT syndrome

MONDO:0000453

A genetic disease of the electrical system of the heart that consists of a constellation of signs and symptoms, consisting of a short QT interval on an EKG (< 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart. Short QT syndrome appears to be inherited in an autosomal dominant pattern, and a few affected families have been identified

Also known as: short QT syndrome, ventricular arrhythmia associated with short QT syndrome, familial short QT syndrome

32 clinical trials for this condition and its sub-types.

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Sub-types

Short QT syndrome 7 (0) Short QT syndrome type 1 (0) Short QT syndrome type 2 (0) Short QT syndrome type 3 (0)

Broader categories

Cardiovascular disorder (1051) Disease (680) Heart disorder (300) Hereditary disease (176) Cardiac rhythm disease (160) Human disease (14) Heart conduction disease (6) Cardiogenetic disease (3) Cardiogenetic rhythm disorder (2) Disease of genetic or genomic mechanism (2)
Trials to join now! 12 Not yet recruiting 3 Not yet finished but already full! 4 Completed 13
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