Long QT syndrome 5

MONDO:0013372

Any long QT syndrome in which the cause of the disease is a mutation in the KCNE1 gene.

Also known as: KCNE1 long QT syndrome, LQT5, long QT syndrome 5, long QT syndrome caused by mutation in KCNE1, long QT syndrome type 5, long QT syndrome 2/5, digenic, long QT syndrome 5, acquired, susceptibility to

1 clinical trial for this condition and its sub-types, 0 tagged with Long QT syndrome 5 itself.

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Where it sits in the disease tree

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↑ Familial long QT syndrome (11)

Sub-types of Long QT syndrome 5

Jervell and Lange-Nielsen syndrome 2 1 trial

Including sub-types (1) Tagged with Long QT syndrome 5 (0)

Not yet finished but already full! 1

Newborn screening study aims to catch rare diseases at birth

Diagnosis Ongoing

This study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…

Sponsor: RTI International • Aim: Diagnosis

Last updated Jul 03, 2026 00:00 UTC

Long QT syndrome 5

Where it sits in the disease tree

Newborn screening study aims to catch rare diseases at birth