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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
achondrogenesis type IB 
acquired mineral metabolism disease 
atelosteogenesis type II 
calcium metabolic disease +   
Disorders in the processing of calcium in the body: its absorption, transport, storage, and utilization. Disorders of calcium metabolism occur when the body has too little or too much calcium. The serum level of calcium is closely regulated within a fairly limited range in the human body. In a healthy physiology, extracellular calcium levels are maintained within a tight range through the actions of parathyroid hormone, vitamin D and the calcium sensing receptor.[1] Disorders in calcium metabolism can lead to hypocalcemia, decreased plasma levels of calcium or hypercalcemia, elevated plasma calcium levels.
chondrodysplasia with joint dislocations, gPAPP type 
COASY protein-associated neurodegeneration 
diastrophic dysplasia 
Fatal multiple mitochondrial dysfunction syndrome +  
iron metabolism disease +   
multiple epiphyseal dysplasia type 4 
phosphorus metabolism disease +   
potassium deficiency disease +   
spondyloepimetaphyseal dysplasia, PAPSS2 type 
spondyloepiphyseal dysplasia with congenital joint dislocations 
sulfur metabolism disease +  

Synonyms
Exact Synonyms: Calcium Metabolism Disorders ;   calcium metabolic disorder ;   disorder of calcium metabolism
Related Synonyms: calcium metabolism disease ;   calcium metabolism disorder
Xrefs: DOID:10575 ;   ICD9:275.4 ;   ICD9:275.40 ;   ICD9:275.49 ;   ICD9CM:275.4 ;   ICD9CM:275.40 ;   MEDGEN:714 ;   MESH:D002128 ;   MONDO:0005557 ;   SCTID:71638002
External Ontologys: disease_disrupts EFO:GO:0055074 ;   participates_in EFO:GO:0008152 ;   participates_in EFO:GO:0055074
Definition Sources: MESH:D002128

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