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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 |