Parent term(s)
Term with siblings
3-methylcrotonyl-CoA carboxylase deficiency +
atrial fibrillation +
atrial standstill 1
atrial standstill 2
atrioventricular block +
atrophic muscular disease +
Brugada syndrome +
catecholaminergic polymorphic ventricular tachycardia +
cysticercosis
diaphragm disease +
epidemic pleurodynia
gas gangrene
left bundle branch hemiblock
muscle benign neoplasm +
muscle cancer +
muscle tissue disease +
postural orthostatic tachycardia syndrome
progressive familial heart block +
right bundle branch block
short QT syndrome
toxocariasis
Wolff-Parkinson-White syndrome
sinoatrial node disease +
3-methylcrotonyl-CoA carboxylase deficiency +
atrial fibrillation +
atrial standstill 1
atrial standstill 2
atrioventricular block +
atrophic muscular disease +
Brugada syndrome +
catecholaminergic polymorphic ventricular tachycardia +
cysticercosis
diaphragm disease +
epidemic pleurodynia
gas gangrene
left bundle branch hemiblock
muscle benign neoplasm +
muscle cancer +
muscle tissue disease +
postural orthostatic tachycardia syndrome
progressive familial heart block +
right bundle branch block
short QT syndrome
toxocariasis
Wolff-Parkinson-White syndrome
Child term(s)
denotes an 'is-a' relationship