Short QT syndrome type 2

MONDO:0012313

Any short QT syndrome in which the cause of the disease is a mutation in the KCNQ1 gene.

Also known as: KCNQ1 short QT syndrome, short QT syndrome caused by mutation in KCNQ1, short QT syndrome type 2, SQT2, short QT syndrome 2

32 clinical trials for this condition and its sub-types, 0 tagged with Short QT syndrome type 2 itself.

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