Long QT syndrome
MONDO:0002442A condition that is characterized by episodes of fainting (syncope) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Romano-Ward syndrome (also known as long QT syndrome 1) and Jervell-Lange Nielsen syndrome.
Also known as: long QT syndrome, ventricular arrhythmia associated with long QT syndrome
29 clinical trials for this condition and its sub-types, 22 tagged with Long QT syndrome itself.
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Sub-types of Long QT syndrome
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Familial long QT syndrome 1 trial · 11 incl. sub-types
19 sub-types
- Long QT syndrome 3 5 trials
- Long QT syndrome 2 3 trials
- Jervell and Lange-Nielsen syndrome 2 trials Sub-types →
- Timothy syndrome 1 trial Sub-types →
- Long QT syndrome 1 1 trial
- Long QT syndrome 5 0 trials · 1 incl. sub-types Sub-types →
- Andersen-Tawil syndrome 0 trials
- Cardiac arrhythmia, ankyrin-B-related 0 trials
- Long QT syndrome 10 0 trials
- Long QT syndrome 11 0 trials
- Long QT syndrome 12 0 trials
- Long QT syndrome 13 0 trials
- Long QT syndrome 14 0 trials
- Long QT syndrome 15 0 trials
- Long QT syndrome 16 0 trials
- Long QT syndrome 4 0 trials
- Long QT syndrome 6 0 trials
- Long QT syndrome 8 0 trials
- Long QT syndrome 9 0 trials