A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24.
synonyms:
BARTS2,
Bartter syndrome type 2 antenatal,
OMIM:241200,
hypokalemic alkalosis with hypercalciuria 2 antenatal,