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Ontology Browser

Term:
3-methylglutaconic aciduria type 1 pathway (PW:0002274)
Annotations: Rat: (30) Mouse: (30) Human: (30) Chinchilla: (30) Bonobo: (30) Dog: (30) Squirrel: (30) Pig: (30)
Parent Terms Term With Siblings Child Terms
3-hydroxyacyl-CoA dehydrogenase deficiency pathway  
3-methylglutaconic aciduria type 1 pathway  
A rare autosomal recessive condition resulting from alterations in leucine metabolism.
3-methylglutaconic aciduria type 3 pathway  
adenine phoshoribosyltransferase deficiency pathway  
AICA-ribosuria pathway  
beta-ureidopropionase deficiency pathway  
fumaric aciduria pathway  
inborn error amino acid transport disorder pathway +   
inborn error of amino acid metabolism pathway +   
inborn error of brain metabolic pathway +   
inborn error of carbohydrate metabolism pathway +   
inborn error of lipid metabolism pathway +   
inborn error of metal metabolism pathway +   
inborn error of purine-pyrimidine metabolism pathway +   
inborn error of renal tubular transport pathway +   
inborn error of steroid metabolism pathway +   
leukotriene C4 synthase deficiency pathway  
lysosomal storage disease pathway +   
malonic aciduria pathway  
porphyria pathway +   

Synonyms
Exact Synonyms: 3-methylglutaconyl-CoA hydratase deficiency pathway ;   3MG-CoA hydratase deficiency pathway ;   MGA type I pathway ;   MGA1 pathway ;   type I 3-Methylglutaconic aciduria disease pathway ;   type I 3-Methylglutaconic aciduria pathway
Related Synonyms: SMP:00139
Definition Sources: OMIM:250950

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