Category
page 1Cardiogenetic disorders
Brugada syndrome
heart conduction disease characterized by abnormal ECG findings
hypertrophic cardiomyopathy
disease in which the heart muscle is enlarged
long QT syndrome
condition involving delayed repolarization of the heart during the heartbeat cycle
Fabry disease
rare human genetic lysosomal storage disorder
dilated cardiomyopathy
disease characterized by an enlarged heart
Alagille syndrome
congenital disorder of digestive system
left bundle branch hemiblock
cardiac conduction abnormality seen on the electrocardiogram
Andersen-Tawil syndrome
Human disease
short QT syndrome
heart conduction disease that is characterized by heart arrhythmia defined as a short QT interval on an EKG (less than 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart
McLeod syndrome
rare disease
Timothy syndrome
autosomal dominant disease that is characterized by cardiac, hand/foot, facial, and neurodevelopmental features; the two forms are type 1 (classic) and type 2, a rare form that has material basis in mutations in a transcript variant of CACNA1C
catecholaminergic polymorphic ventricular tachycardia
disorder characterized by an abnormal heart rhythm (arrhythmia)
left anterior fascicular block
abnormal condition of the condution of the heart