syndromic disease renal tubular transport disease Bartter syndrome Bartter disease Bartter syndrome is a group of rare renal tubular disease characterized by impaired salt reabsorption in the thick ascending limb of Henle's loop and clinically by the association of hypokalemic alkalosis, hypercalciuria/nephrocalcinosis, increased levels of plasma renin and aldosterone, low blood pressure and vascular resistance to angiotensin II. Bartter's syndrome COHD:45769152 DOID:445 GARD:0005893 ICD10:E26.8 ICD10:E26.81 ICD9:255.13 MESH:D001477 MONDO:0015231 MedDRA:10050839 NCIT:C34412 OMIMPS:601678 Orphanet:112 Potassium wasting SCTID:707742001 UMLS:C0004775 UMLS:C0085570 aldosteronism with hyperplasia of the adrenal cortex https://rarediseases.info.nih.gov/diseases/5893/bartter-syndrome hypokalemic alkalosis hypokalemic alkalosis with hypercalciuria renal tubular normotensive hypokalemic alkalosis with hypercalciuria salt-losing tubular disorder, Henle's loop type salt-wasting tubulopathy, Henle's loop type inherited renal tubular disease