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Term:
lysosomal storage disease pathway
(PW:0001630)
Annotations:
Rat: (70)
Mouse: (70)
Human: (71)
Chinchilla: (69)
Bonobo: (71)
Dog: (69)
Squirrel: (68)
Pig: (70)
Naked Mole-rat: (69)
Green Monkey: (71)
Parent Terms
Term With Siblings
Child Terms
inborn error of metabolism pathway
+
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
+
cholesterol ester storage disease pathway
+
cystinosis pathway
+
mucopolysaccharidoses pathway
nervous system lysosomal storage disease pathway
+
Synonyms
Related Synonyms:
lysosomal storage disorders
Definition Sources:
PMID:25275857