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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
cerebral creatine deficiency syndrome +  
disorder of beta and omega amino acid metabolism +  
Disorder of cobalamin metabolism and transport +  
disorder of glutamine metabolism +  
disorder of melanin metabolism +  
disorder of phenylalanine metabolism +  
disorder of tyrosine metabolism +  
disorders of vitamin D metabolism +  
familial isolated deficiency of vitamin E 
gamma-amino butyric acid metabolism disorder +  
Hypocalcemic vitamin D-dependent rickets 
Hypocalcemic vitamin D-resistant rickets 
inborn disorder of aspartate family metabolism +  
inborn disorder of bile acid synthesis +  
inborn disorder of branched-chain amino acid metabolism +  
inborn disorder of cobalamin metabolism and transport +  
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 or proline metabolism +  
inborn disorder of pyridoxine metabolism +  
inborn disorder of serine family metabolism +  
inborn disorder of the gamma-glutamyl cycle +  
inborn disorder of tryptophan metabolism +  
inborn error of biotin metabolism +  
Infantile spams - psychomotor retardation - progressive brain atrophy - basal ganglia disease 
inherited fatty acid metabolism disorder +  
neurodegenerative syndrome due to cerebral folate transport deficiency 
pyruvate metabolism disorder +  
Thiamine-responsive encephalopathy 
urea cycle disorder +  
X-linked hypophosphatemia 

Synonyms
Alternate IDs: MONDO:0020698

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