A hereditary cardiac disease characterized by a prolongation of the QT interval at basal ECG and by a high risk of life-threatening arrhythmias.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Timothy syndrome | MONDO:0010979 | 4 | |
| Jervell and Lange-Nielsen syndrome | MONDO:0002441 | 2 | |
| Long QT syndrome 5 | MONDO:0013372 | 1 | KCNE1 |
| Andersen-Tawil syndrome | MONDO:0008222 | KCNJ2 | |
| Cardiac arrhythmia, ankyrin-B-related | MONDO:0010958 | ANK2 | |
| Long QT syndrome 1 | MONDO:0100316 | KCNQ1 | |
| Long QT syndrome 10 | MONDO:0012737 | SCN4B | |
| Long QT syndrome 11 | MONDO:0012738 | AKAP9 | |
| Long QT syndrome 12 | MONDO:0013062 | SNTA1 | |
| Long QT syndrome 13 | MONDO:0013279 | KCNJ5 | |
| Long QT syndrome 14 | MONDO:0014548 | CALM1 | |
| Long QT syndrome 15 | MONDO:0014550 | CALM2 | |
| Long QT syndrome 16 | MONDO:0032915 | ||
| Long QT syndrome 2 | MONDO:0013367 | KCNH2 | |
| Long QT syndrome 3 | MONDO:0011377 | ||
| Long QT syndrome 4 | MONDO:0800323 | ||
| Long QT syndrome 6 | MONDO:0013370 | KCNE2 | |
| Long QT syndrome 8 | MONDO:0032756 | ||
| Long QT syndrome 9 | MONDO:0012736 | CAV3 |
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