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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 +   
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 +   
A metabolic disorder that affects the phosphate homeostasis.
potassium deficiency disease +   
spondyloepimetaphyseal dysplasia, PAPSS2 type 
spondyloepiphyseal dysplasia with congenital joint dislocations 
sulfur metabolism disease +  

Synonyms
Exact Synonyms: disorder of phosphorus metabolism ;   phosphorus disorder ;   phosphorus metabolic disorder ;   phosphorus metabolism disorder
Alternate IDs: MONDO:0002319
Xrefs: DOID:2485 ;   ICD10CM:E83.3 ;   ICD9:275.3 ;   MEDGEN:19276 ;   MESH:D010760 ;   NCI:C97095 ;   SCTID:87049008 ;   UMLS:C0031707
External Ontologys: disease_disrupts EFO:GO:0006793
Definition Sources: NCIT:C97095

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