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Bartter syndrome

Disease Summary
Associated Targets (9)
Tchem

4

Tclin

3

Tbio

2


Explore Associated Targets
Mondo Description 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.
Mondo Term and Equivalent IDs
MONDO:0015231:  Bartter syndrome
COHD:45769152: 
GARD:0005893: 
ICD9:255.13: 
MESH:D001477: 
NCIT:C34412: 
OMIMPS:601678: 
Orphanet:112: 
SCTID:707742001: 
UMLS:C0004775: 
UMLS:C0085570: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)