Short QT syndrome type 3

MONDO:0012314

Any short QT syndrome in which the cause of the disease is a mutation in the KCNJ2 gene.

Also known as: KCNJ2 short QT syndrome, short QT syndrome caused by mutation in KCNJ2, short QT syndrome type 3, SQT3, short QT syndrome 3

32 clinical trials for this condition and its sub-types, 0 tagged with Short QT syndrome type 3 itself.

Where it sits in the disease tree

Part of

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.