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Ontology Browser

Term:
inborn error of lipid metabolism pathway (PW:0001643)
Annotations: Rat: (95) Mouse: (95) Human: (95) Chinchilla: (92) Bonobo: (93) Dog: (94) Squirrel: (93) Pig: (94)
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  
hypercholesterolemia 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 +   
Those diseases that are caused by inborn errors of lipid metabolism. The mutations can disrupt one or several pathways.
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 +   
xanthomatosis pathway +   

Synonyms
Exact Synonyms: inborn error of lipid metabolism disease pathway
Definition Sources: MeSH:D008052

paths to the root