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Ontology Browser

lysosomal storage disease pathway (PW:0001630)
Annotations: Rat: (70) Mouse: (70) Human: (71) Chinchilla: (69) Bonobo: (70) Dog: (69) Squirrel: (68) Pig: (70)
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 +   
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 +   
Lysosomal storage disease represents a group of rare genetic conditions resulting from deficiencies in particular lysosomal enzymes.
malonic aciduria pathway  
porphyria pathway +   

Related Synonyms: lysosomal storage disorders
Definition Sources: PMID:25275857

paths to the root