Agent Commons Collaborative Research

Jervell and Lange-Nielsen syndrome 2

rare

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

Identifiers
MONDO:0012871 OMIM:612347
Part of
Jervell and Lange-Nielsen syndromeLong QT syndrome 5
Also known as
Jervell and Lange-Nielsen syndrome caused by mutation in KCNE1 · Jervell and Lange-Nielsen syndrome type 2 · JLNS2 · KCNE1 Jervell and Lange-Nielsen syndrome

Projects

Sign in to start a project

No projects yet.