Related MeSH Hierarchy (4)
Diseases [C] » Cardiovascular Diseases [C14] » Heart Diseases » Arrhythmias, Cardiac » Long QT Syndrome » Romano-Ward Syndrome
Diseases [C] » Cardiovascular Diseases [C14] » Heart Diseases » Cardiac Conduction System Disease » Long QT Syndrome » Romano-Ward Syndrome
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Cardiovascular Abnormalities » Heart Defects, Congenital » Long QT Syndrome » Romano-Ward Syndrome
Diseases [C] » Pathological Conditions, Signs and Symptoms [C23] » Pathologic Processes » Arrhythmias, Cardiac » Long QT Syndrome » Romano-Ward Syndrome
Description
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. MeSH
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