Jervell and Lange-Nielsen syndrome 1

Any Jervell and Lange-Nielsen syndrome in which the cause of the disease is a mutation in the KCNQ1 gene.

Also known as: Jervell and Lange-Nielsen syndrome, Jervell and Lange-Nielsen syndrome 1, Jervell and Lange-Nielsen syndrome caused by mutation in KCNQ1, KCNQ1 Jervell and Lange-Nielsen syndrome, Cardioauditory syndrome of Jervell and Lange-Nielsen, JLNS1, Surdo-Cardiac syndrome, deafness, congenital, and functional heart disease

1 clinical trial for this condition and its sub-types.