disease has basis in dysfunction of SLC12A3 syndromic disease renal tubular transport disease Gitelman syndrome DOID:0050450 GARD:0008547 GTLMNS Gitelman syndrome Gitelman syndrome (GS), also referred to as familial hypokalemia-hypomagnesemia, is characterized by hypokalemic metabolic alkalosis in combination with significant hypomagnesemia and low urinary calcium excretion. Gitelman's syndrome ICD10:N15.8 ICD9:275.49 MESH:D053579 MONDO:0009904 MedDRA:10062906 NCIT:C84730 OMIM:263800 Orphanet:358 Potassium and magnesium depletion SCTID:707756004 UMLS:C0268450 familial hypokalemia-hypomagnesemia https://rarediseases.info.nih.gov/diseases/8547/gitelman-syndrome hypomagnesemia-hypokalemia, primary renotubular, with hypocalciuria primary renal tubular hypokalemic hypomagnesemia with hypocalciuria inherited renal tubular disease