KCNH2

potassium voltage-gated channel subfamily H member 2
OMIM: 152427
PanelMode of inheritanceDetails
2 panels
Component of the following Super Panels:
  • - Cardiac arrhythmias
  • - Sudden unexplained death or survivors of a cardiac event
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R127
Signed-off version 3.8
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Short QT syndrome 1 (609620), Long QT syndrome-2, Long QT syndrome-2 (613688)
Component of the following Super Panels:
  • - Cardiac arrhythmias
  • - Sudden unexplained death or survivors of a cardiac event
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R130
Signed-off version 3.12
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Brugada, Short QT syndrome 1 (609620), ventricular fibrillation, cardiac arrest, Short QT syndrome 1 609620, Long QT syndrome-2 (613688), short qt, atrial fibrillation