Template:Inborn errors of carbohydrate metabolism

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v • d • e Inborn error of carbohydrate metabolism (including glycogen storage diseases) (E73-74, 271)
Disaccharide catabolism	Lactose intolerance - Sucrose intolerance
Monosaccharide catabolism	fructose: Essential fructosuria - Fructose intolerance galactose/galactosemia : Galactokinase deficiency - Galactose-1-phosphate uridylyltransferase galactosemia - Galactose epimerase deficiency
Monosaccharide transport	Glucose-galactose malabsorption - Inborn errors of renal tubular transport (Renal glycosuria)
Glycolysis	GSD type VII, Tarui's, phosphofructokinase - Triosephosphate isomerase deficiency - Pyruvate kinase deficiency
Pyruvate catabolism	PDHA - Fumarase deficiency
Gluconeogenesis	PCD - Fructose bisphosphatase deficiency - GSD type I, von Gierke, glucose 6-phosphatase
Glycogenesis	GSD type 0, glycogen synthase - GSD type IV, Andersen's, branching
Glycogenolysis	GSD type II, Pompe's, glucosidase - GSD type III, Cori's, debranching - GSD type V, McArdle, glycogen phosphorylase/GSD type VI, Hers', glycogen phosphorylase - GSD type I, von Gierke, glucose 6-phosphatas
Pentose phosphate pathway	Glucose-6-phosphate dehydrogenase deficiency - Pentosuria
Other	Hyperoxaluria
see also glycolysis enzymes, pentose phosphate pathway enzymes, fructose and galactose metabolism enzymes