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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.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:4479
MESH:D011546
NCIT:C85034
Orphanet:444916
SCTID:77098009
UMLS:C0033805
MONDO:0018638
High level summary of knowledge for a disease, including descriptions and datasource references.