Cure My Disease

Don't miss your cure!

Home News Browse About
Log in / Sign up

Jervell and Lange-Nielsen syndrome 2

MONDO:0012871

Any Jervell and Lange-Nielsen syndrome in which the cause of the disease is a mutation in the KCNE1 gene.

Also known as: Jervell and Lange-Nielsen syndrome 2, Jervell and Lange-Nielsen syndrome caused by mutation in KCNE1, Jervell and Lange-Nielsen syndrome type 2, KCNE1 Jervell and Lange-Nielsen syndrome, JLNS2

1 clinical trial 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) Jervell and Lange-Nielsen syndrome (2) Disease by body system or component (0) Disease by etiologic mechanism (0) Familial long QT syndrome (0)
Not yet finished but already full! 1
Sort by
  • 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

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse About Terms of use Contact us

This is a site from Cyber and Space