Bartter disease type 2

Any Bartter syndrome in which the cause of the disease is a mutation in the KCNJ1 gene.

Also known as: BARTS2, Bartter disease type 2, Bartter syndrome caused by mutation in KCNJ1, Bartter syndrome type 2, Bartter syndrome, type 2, KCNJ1 Bartter syndrome, hyperprostaglandin E syndrome 2, Bartter syndrome antenatal type 2

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