Long QT Syndrome 2
An autosomal dominant condition caused by mutation(s) in the KCNH2 gene, encoding potassium voltage-gated channel subfamily H member 2. It is characterized by a prolonged QT interval that may result in torsade de pointes, ventricular fibrillation and/or sudden cardiac death.
C137957
C3150943
Cellosaurus
Disease or Syndrome
LQT2
Long QT Syndrome 2
Long QT Syndrome 2
Cellosaurus Disease Terminology
Cellosaurus Terminology
Long QT Syndrome