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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Bartter syndrome +  
Dent disease +  
familial renal glucosuria 
Fanconi renotubular syndrome +  
Gitelman syndrome 
Liddle syndrome +  
pseudohypoaldosteronism +  
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.
renal hypomagnesemia 3 
renal tubular acidosis +  

Synonyms
Exact Synonyms: DOID:4479 ;   NCIT:C85034 ;   Orphanet:444916 ;   http://identifiers.org/medgen/18721 ;   http://identifiers.org/mesh/D011546 ;   http://identifiers.org/snomedct/77098009 ;   http://linkedlifedata.com/resource/umls/id/C0033805
Alternate IDs: MONDO:0018638
Xrefs: DOID:4479 ;   GARD:21861 ;   ICD9:255.8 ;   MEDGEN:18721 ;   MESH:D011546 ;   NANDO:2100133 ;   NANDO:2200367 ;   NCI:C85034 ;   ORDO:444916 ;   SCTID:77098009
Definition Sources: NCIT:C85034

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