Familial long QT syndrome
MONDO:0019171A 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
11 clinical trials for this condition and its sub-types, 1 tagged with Familial long QT syndrome itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Familial long QT syndrome
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Long QT syndrome 3 6 trials
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Long QT syndrome 2 3 trials
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Jervell and Lange-Nielsen syndrome 2 trials
2 sub-types
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Timothy syndrome 1 trial
2 sub-types
- Timothy syndrome, classic type 0 trials · 1 incl. sub-types Sub-types →
- Timothy syndrome, atypical type 0 trials
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Long QT syndrome 1 1 trial
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Long QT syndrome 5 0 trials · 1 incl. sub-types
1 sub-type
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Andersen-Tawil syndrome 0 trials
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Long QT syndrome 10 0 trials
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Long QT syndrome 11 0 trials
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Long QT syndrome 12 0 trials
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Long QT syndrome 13 0 trials
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Long QT syndrome 14 0 trials
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Long QT syndrome 15 0 trials
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Long QT syndrome 16 0 trials
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Long QT syndrome 4 0 trials
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Long QT syndrome 6 0 trials
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Long QT syndrome 8 0 trials
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Long QT syndrome 9 0 trials