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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
biotin metabolic disease +  
cerebral creatine deficiency syndrome +  
creatine biosynthetic process disease +  
disorder of fatty acid oxidation and ketogenesis +  
disorder of phenylalanine metabolism +  
disorder of tyrosine metabolism +  
gamma-amino butyric acid metabolism disorder +  
glycine metabolism disease +  
inborn disorder of amino acid metabolism +   
inborn disorder of aspartate family metabolism +  
inborn disorder of bile acid synthesis +  
inborn disorder of branched-chain amino acid metabolism +  
inborn disorder of gamma-aminobutyric acid metabolism 
inborn disorder of histidine metabolism +  
inborn disorder of methionine cycle and sulfur amino acid metabolism +  
inborn disorder of ornithine metabolism +  
inborn disorder of proline metabolism +  
inborn disorder of serine family metabolism +  
inborn disorder of tryptophan metabolism +  
inherited lipoic acid biosynthesis defect +  
pyruvate metabolism disorder +  
scurvy 
valine metabolism disease +  
A disease that has its basis in the disruption of valine metabolic process.

Synonyms
Exact Synonyms: disorder of valine metabolic process ;   disorder of valine metabolism ;   valine metabolic process disease
Alternate IDs: MONDO:0037870
Xrefs: MEDGEN:753614 ;   SCTID:444756000 ;   UMLS:C2919304
Definition Sources: MONDO:design_pattern

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