Long Qt Syndrome 2

A congenital disorder characterized by a prolonged QT interval and TORSADE DE POINTES. These cardiac arrhythmias may result in recurrent SYNCOPE, seizure, or sudden death. Mutations in the KCNH2 gene have been identified. OMIM: 613688

Cardiovascular Diseases: 94258
- Heart Diseases: 26486
  - Cardiac Arrhythmias: 21201
    - Long QT Syndrome: 1864
      - Long Qt Syndrome 2: 12
  - Cardiac Conduction System Disease: 95
    - Long QT Syndrome: 1864
      - Long Qt Syndrome 2: 12
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Congenital Abnormalities: 26404
  - Cardiovascular Abnormalities: 457
    - Congenital Heart Defects: 9139
      - Long QT Syndrome: 1864
        Long Qt Syndrome 2: 12
Signs and Symptoms Pathological Conditions
- Pathologic Processes: 10385
  - Cardiac Arrhythmias: 21201
    - Long QT Syndrome: 1864
      - Long Qt Syndrome 2: 12

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