|
MIM:615441 - CARDIAC ARRHYTHMIA SYNDROME, WITH OR WITHOUT SKELETAL MUSCLE WEAKNESS; CARDAR
Xenbase Genes: trdn
Human Disease Resource: MIM
| MONDO:0014191 - catecholaminergic polymorphic ventricular tachycardia 5 |
| MONDO:0017990 - catecholaminergic polymorphic ventricular tachycardia |
| DOID:0060679 - catecholaminergic polymorphic ventricular tachycardia 5 |
