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Term:
Parent Terms Term With Siblings Child Terms
achondrogenesis type IB 
acquired mineral metabolism disease 
atelosteogenesis type II 
calcium metabolic disease +   
chondrodysplasia with joint dislocations, gPAPP type 
COASY protein-associated neurodegeneration 
diastrophic dysplasia 
eating disorder +   
Fatal multiple mitochondrial dysfunction syndrome +  
hemorrhagic disease of newborn 
iron metabolism disease +   
lactose intolerance +  
malnutrition 
multiple epiphyseal dysplasia type 4 
nutritional deficiency disease +   
overnutrition +   
phosphorus metabolism disease +   
potassium deficiency disease +   
Any disorder caused by an insufficient amount or availability of potassium, which generally manifests with myalgia, tetany, hypotension, polyuria, and polydipsia.
spondyloepimetaphyseal dysplasia, PAPSS2 type 
spondyloepiphyseal dysplasia with congenital joint dislocations 
sulfur metabolism disease +  

Synonyms
Exact Synonyms: hypokalemia
Related Synonyms: hypopotassemia ;   potassium deficiency disorder
Alternate IDs: MONDO:0003019
Xrefs: DOID:4500 ;   HP:0002900 ;   ICD10CM:E87.6 ;   ICD9:276.8 ;   MEDGEN:271346 ;   MESH:D007008 ;   NCI:C34939 ;   SCTID:43339004 ;   UMLS:C1514284
Definition Sources: NCIT:P378

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