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Cardiovascular Diseases > Heart Diseases > Heart Defects, Congenital > Long QT Syndrome > Romano-Ward Syndrome
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Cardiovascular Abnormalities > Heart Defects, Congenital > Long QT Syndrome > Romano-Ward Syndrome
Cardiovascular Diseases > Cardiovascular Abnormalities > Heart Defects, Congenital > Long QT Syndrome > Romano-Ward Syndrome
Cardiovascular Diseases > Heart Diseases > Arrhythmias, Cardiac > Long QT Syndrome > Romano-Ward Syndrome
Pathological Conditions, Signs and Symptoms > Pathologic Processes > Arrhythmias, Cardiac > Long QT Syndrome > Romano-Ward Syndrome
Cardiovascular Diseases > Heart Diseases > Cardiac Conduction System Disease > Long QT Syndrome > Romano-Ward Syndrome

Término preferido

Romano-Ward Syndrome  

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Tipo

  • mesh:Descriptor

Definición

  • A form of long QT syndrome that is without congenital deafness. It is caused by mutation of the KCNQ1 gene which encodes a protein in the VOLTAGE-GATED POTASSIUM CHANNEL.

Concepto genérico

Etiquetas alternativas

  • Long QT Syndrome 1
  • Long QT Syndrome Type 1
  • Ventricular Fibrillation with Prolonged QT Interval
  • Ward-Romano Syndrome

En otras lenguas

URI

http://data.loterre.fr/ark:/67375/JVR-XF68Z9GR-H

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RDF/XML TURTLE JSON-LD Creado 25/7/01, última modificación 20/6/17