A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24.
synonyms:
hyperprostaglandin E syndrome 2,
BARTS2,
ICD10CM:E26.8,
hypokalemic alkalosis with hypercalciuria 2 antenatal,