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Familial long QT syndrome

MONDO:0019171

A hereditary cardiac disease characterized by a prolongation of the QT interval at basal ECG and by a high risk of life-threatening arrhythmias.

Also known as: LQTS, Long QT Syndrome, Romano-Ward long QT syndrome, Romano-Ward syndrome, Ward-Romano syndrome, congenital long QT syndrome, familial long QT syndrome, hereditary long QT syndrome

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

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Sub-types

Long QT syndrome 3 (5) Long QT syndrome 2 (3) Jervell and Lange-Nielsen syndrome (2) Jervell and Lange-Nielsen syndrome 1 (1) Jervell and Lange-Nielsen syndrome 2 (1) Long QT syndrome 1 (1) Timothy syndrome (1) Timothy syndrome type 1 (1) Andersen-Tawil syndrome (0) Cardiac arrhythmia, ankyrin-B-related (0) Long QT syndrome 10 (0) Long QT syndrome 11 (0) Long QT syndrome 12 (0) Long QT syndrome 13 (0) Long QT syndrome 14 (0) Long QT syndrome 15 (0) Long QT syndrome 16 (0) Long QT syndrome 4 (0) Long QT syndrome 5 (0) Long QT syndrome 6 (0)

Broader categories

Disease (618) Hereditary disease (172) Syndromic disease (24) Long QT syndrome (18) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)
Trials to join now! 3 Not yet recruiting 2 Not yet finished but already full! 3 Completed 2
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