Inborn errors of carbohydrate metabolism
6-phosphogluconate dehydrogenase deficiencyAdult polyglucosan body diseaseAldolase A deficiencyEnolase deficiencyEssential fructosuriaFanconi–Bickel syndromeFructose bisphosphatase deficiencyFructose malabsorptionGalactokinase deficiencyGalactose-1-phosphate uridylyltransferase deficiencyGalactosemiaGalactosemic cataractGlucose-6-phosphate dehydrogenase deficiencyGlucose-galactose malabsorptionGlycogen storage diseaseGlycogen storage disease type 0Glycogen storage disease type IGlycogen storage disease type IIGlycogen storage disease type IIIGlycogen storage disease type IVGlycogen storage disease type VGlycogen storage disease type VIHereditary fructose intoleranceHexokinase deficiencyHyperoxaluriaInborn errors of carbohydrate metabolismPentosuriaPhosphofructokinase deficiencyPyruvate carboxylase deficiencyPyruvate kinase deficiencySucrose intoleranceTransaldolase deficiencyTriosephosphate isomerase deficiency
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6-phosphogluconate dehydrogenase deficiencyAdult polyglucosan body diseaseAldolase A deficiencyEnolase deficiencyEssential fructosuriaFanconi–Bickel syndromeFructose bisphosphatase deficiencyFructose malabsorptionGalactokinase deficiencyGalactose-1-phosphate uridylyltransferase deficiencyGalactosemiaGalactosemic cataractGlucose-6-phosphate dehydrogenase deficiencyGlucose-galactose malabsorptionGlycogen storage diseaseGlycogen storage disease type 0Glycogen storage disease type IGlycogen storage disease type IIGlycogen storage disease type IIIGlycogen storage disease type IVGlycogen storage disease type VGlycogen storage disease type VIHereditary fructose intoleranceHexokinase deficiencyHyperoxaluriaInborn errors of carbohydrate metabolismPentosuriaPhosphofructokinase deficiencyPyruvate carboxylase deficiencyPyruvate kinase deficiencySucrose intoleranceTransaldolase deficiencyTriosephosphate isomerase deficiency
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Inborn errors of carbohydrate metabolism
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Inborn errors of carbohydrate metabolism
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Inborn errors of carbohydrate metabolism
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