"classic Bartter syndrome"@en . "ICD10CM:E26.8"^^ . "BARTS3"@en . "GARD:9659"^^ . . . "A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the kidney chloride channel B gene (CLCNKB) on chromosome 1p36."^^ . "DOID:0110144"^^ . "disease_ontology"^^ . "OMIM:607364"^^ . . "Bartter syndrome type 3"@en . "Bartter disease type 3"^^ .