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Ontology Browser

Term:
inborn error of amino acid metabolism pathway (PW:0001645)
Annotations: Rat: (229) Mouse: (229) Human: (232) Chinchilla: (216) Bonobo: (226) Dog: (228) Squirrel: (222) Pig: (227)
Parent Terms Term With Siblings Child Terms
3-hydroxyacyl-CoA dehydrogenase deficiency pathway  
3-methylglutaconic aciduria type 1 pathway  
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 +   
Those diseases that are caused by inborn errors of amino acid metabolism. The mutations can disrupt one or several pathways.
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: inborn error of amino acid metabolism disease pathway
Definition Sources: MeSH:D000592

paths to the root