Any variation from the normal rate or rhythm (which may include the origin of the impulse and/or its subsequent propagation) in the heart.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Cardiogenetic rhythm disorder | MONDO:1010180 | 59 | |
| Atrial fibrillation | MONDO:0004981 | 23 | |
| Ventricular tachycardia | MONDO:0005477 | 11 | |
| Cardiac conduction defect | MONDO:0100042 | 9 | |
| Ventricular fibrillation | MONDO:0000190 | 3 | |
| Atrial tachycardia | MONDO:0005479 | 2 | |
| Cardiac conduction disease with or without cardiomyoopathy | MONDO:0980715 | 2 | |
| His bundle tachycardia | MONDO:0017989 | ||
| Cardiac arrest | MONDO:0000745 | ||
| Incessant infant ventricular tachycardia | MONDO:0018685 | ||
| Multifocal atrial tachycardia | MONDO:0017988 | ||
| Sino-auricular heart block | MONDO:0015257 | ||
| Sinoatrial node dysfunction and deafness | MONDO:0013960 | CACNA1D | |
| Sudden arrhythmia death syndrome | MONDO:0054866 | ||
| Sudden cardiac arrest | MONDO:0100511 | ||
| Torsade-de-pointes syndrome with short coupling interval | MONDO:0013317 | ||
| Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome | MONDO:0020745 | RYR2 |
Rare disease
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