Long QT syndrome 6

MONDO:0013370

Any long QT syndrome in which the cause of the disease is a mutation in the KCNE2 gene.

Also known as: KCNE2 long QT syndrome, LQT6, long QT syndrome 6, long QT syndrome caused by mutation in KCNE2, long QT syndrome type 6, long QT syndrome 3/6, digenic, long QT syndrome 6, acquired, susceptibility to

0 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (618) Hereditary disease (172) Syndromic disease (24) Long QT syndrome (18) Human disease (14) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0) Familial long QT syndrome (0)

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