Disease_Mapped_To_Gene
Cellosaurus Disease Terminology
Cellosaurus Terminology
Long QT Syndrome
KCNQ1 Gene
Long QT Syndrome 1
An autosomal dominant condition caused by mutation(s) in the KCNQ1 gene, encoding potassium voltage-gated channel subfamily KQT member 1. It is characterized by a prolonged QT interval that may result in torsade de pointes, ventricular fibrillation and/or sudden cardiac death.
C0035828
C85049
Cellosaurus
Disease or Syndrome
LQT1
Long QT Syndrome 1
Long QT Syndrome 1
Romano-Ward Syndrome