You are using an outdated browser. Please upgrade your browser to improve your experience.

pseudohypoaldosteronism

Disease Summary
Associated Targets (13)
Tbio

8

Tclin

4

Tchem

1


Mondo Description An inherited or acquired disorder of electrolyte metabolism, characterized by the inability of the renal tubules to respond to aldosterone. It is manifested by hyperkalemic metabolic acidosis, urinary salt wasting, normal or increased aldosterone secretion and normal glomerular filtration rate.
Mondo Term and Equivalent IDs
MONDO:0018638:  pseudohypoaldosteronism
MESH:D011546: 
NCIT:C85034: 
Orphanet:444916: 
SCTID:77098009: 
UMLS:C0033805: