Misplaced Pages

The following pages link to Fructose bisphosphatase deficiency

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Showing 50 items.

• Glucose (links | edit)
• Fructose (links | edit)
• Sucrose (links | edit)
• Lactose intolerance (links | edit)
• Glycogen storage disease type V (links | edit)
• Glycogen storage disease (links | edit)
• Congenital disorder of glycosylation (links | edit)
• Lactic acidosis (links | edit)
• Fructose 1,6-bisphosphatase (links | edit)
• Glucose-6-phosphate dehydrogenase deficiency (links | edit)
• Galactosemia (links | edit)
• Phosphoglucomutase (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)
• Fructose-1,6-diphosphatase deficiency (redirect page) (links | edit)
  • List of MeSH codes (C18) (links | edit)
  • List of MeSH codes (C16) (links | edit)
  • List of causes of hypoglycemia (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)
• Essential fructosuria (links | edit)
• Galactose-1-phosphate uridylyltransferase deficiency (links | edit)
• Glucose-galactose malabsorption (links | edit)
• Mitochondrial pyruvate carrier 2 (links | edit)
• Monocarboxylate transporter 1 (links | edit)
• Enzyme-activated MR contrast agents (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)
• 6-phosphogluconate dehydrogenase deficiency (links | edit)
• Transaldolase deficiency (links | edit)
• Danon disease (links | edit)