disease has basis in dysfunction of KCNJ1 Bartter disease type 2 Any Bartter syndrome in which the cause of the disease is a mutation in the KCNJ1 gene. BARTS2 Bartter syndrome antenatal type 2 Bartter syndrome caused by mutation in KCNJ1 Bartter syndrome type 2 Bartter syndrome type 2 antenatal Bartter syndrome, antenatal, type 2 Bartter syndrome, type 2, antenatal DOID:0110143 GARD:0009658 ICD10:E26.8 KCNJ1 Bartter syndrome MESH:C537651 MONDO:0009424 OMIM:241200 SCTID:700109009 hyperprostaglandin E syndrome 2 hypokalemic alkalosis with hypercalciuria 2 antenatal hypokalemic alkalosis with hypercalciuria 2, antenatal hypokalemic alkalosis with hypercalciuria antenatal 2 hypokalemic alkalosis with hypercalciuria, antenatal, 2 Bartter syndrome