Misplaced Pages

The following pages link to Essential fructosuria

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Showing 50 items.

• Glucose (links | edit)
• Fructose (links | edit)
• Sucrose (links | edit)
• Lactose intolerance (links | edit)
• Hexokinase (links | edit)
• Glycogen storage disease type V (links | edit)
• Glycogen storage disease (links | edit)
• Congenital disorder of glycosylation (links | edit)
• Fructose bisphosphatase deficiency (links | edit)
• Glucose-6-phosphate dehydrogenase deficiency (links | edit)
• Galactosemia (links | edit)
• Phosphoglucomutase (links | edit)
• Asymptomatic (links | edit)
• Fructose malabsorption (links | edit)
• Hereditary fructose intolerance (links | edit)
• Hyperinsulinemic hypoglycemia (links | edit)
• Glycogen storage disease type II (links | edit)
• Phosphofructokinase deficiency (links | edit)
• Pyruvate kinase deficiency (links | edit)
• Inborn errors of metabolism (links | edit)
• Glycogen storage disease type I (links | edit)
• Transketolase (links | edit)
• Glycogen storage disease type IV (links | edit)
• Glycogen storage disease type III (links | edit)
• Glycogen storage disease type 0 (links | edit)
• List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
• Pyruvate carboxylase deficiency (links | edit)
• Hyperoxaluria (links | edit)
• Sucrose intolerance (links | edit)
• Triosephosphate isomerase deficiency (links | edit)
• Galactokinase deficiency (links | edit)
• Aldolase A deficiency (links | edit)
• Glycogen storage disease type VI (links | edit)
• Renal glycosuria (links | edit)
• Pentosuria (links | edit)
• Galactose epimerase deficiency (links | edit)
• Hepatic fructokinase (links | edit)
• Galactose-1-phosphate uridylyltransferase deficiency (links | edit)
• Fructosuria (redirect page) (links | edit)
  • List of diseases (F) (links | edit)
  • Fructokinase (links | edit)
  • User talk:Anandks007/Med (links | edit)
  • User talk:Pippin2k (links | edit)
  • Misplaced Pages:Articles for creation/2006-01-04 (links | edit)
• Glucose-galactose malabsorption (links | edit)
• Mitochondrial pyruvate carrier 2 (links | edit)
• Monocarboxylate transporter 1 (links | edit)
• Primary hyperoxaluria (links | edit)
• Hexokinase deficiency (links | edit)
• Galactosemic cataract (links | edit)
• Glycogen storage disease type IX (links | edit)
• Inborn errors of carbohydrate metabolism (links | edit)
• Fructolysis (links | edit)
• 6-phosphogluconate dehydrogenase deficiency (links | edit)
• Transaldolase deficiency (links | edit)