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pseudohypoaldosteronism

Go to external page http://purl.obolibrary.org/obo/MONDO_0018638

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. [ NCIT:C85034 ]

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0033805 (Orphanet:444916)
  • NCIT:C85034 (MONDO:equivalentTo)
  • DOID:4479 (MONDO:equivalentTo)
  • Orphanet:444916 (MONDO:equivalentTo)
  • ICD9:255.8 (MONDO:relatedTo)
  • SCTID:77098009 (MONDO:equivalentTo)
  • MESH:D011546 (MONDO:equivalentTo)
  • GARD:21861 (Orphanet:444916)
Subsets

gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders

exactMatch

http://linkedlifedata.com/resource/umls/id/C0033805

http://www.orpha.net/ORDO/Orphanet_444916

http://purl.obolibrary.org/obo/DOID_4479

http://identifiers.org/snomedct/77098009

http://identifiers.org/mesh/D011546

http://purl.obolibrary.org/obo/NCIT_C85034

id

MONDO:0018638

Term relations