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Pathological Conditions, Signs and Symptoms > Pathologic Processes > Arrhythmias, Cardiac > Long QT Syndrome > Romano-Ward Syndrome
Cardiovascular Diseases > Heart Diseases > Arrhythmias, Cardiac > Long QT Syndrome > Romano-Ward Syndrome
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 > Cardiac Conduction System Disease > Long QT Syndrome > Romano-Ward Syndrome

Preferred term

Romano-Ward Syndrome  

Type

  • Topical Descriptor

Broader concept

Entry terms

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

Scope note

  • 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.

History note

  • 2002; use LONG QT SYNDROME 1986-2001

In other languages

URI

http://www.yso.fi/onto/mesh/D029597

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