The following pages link to Template:Inborn errors of carbohydrate metabolism
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Glucose (transclusion) (links | edit)
- Fructose (transclusion) (links | edit)
- Sucrose (transclusion) (links | edit)
- Lactose intolerance (transclusion) (links | edit)
- Glycogen storage disease type V (transclusion) (links | edit)
- Glycogen storage disease (transclusion) (links | edit)
- Congenital disorder of glycosylation (transclusion) (links | edit)
- Fructose bisphosphatase deficiency (transclusion) (links | edit)
- Glucose-6-phosphate dehydrogenase deficiency (transclusion) (links | edit)
- Galactosemia (transclusion) (links | edit)
- Phosphoglucomutase (transclusion) (links | edit)
- Fructose malabsorption (transclusion) (links | edit)
- Hereditary fructose intolerance (transclusion) (links | edit)
- Hyperinsulinemic hypoglycemia (transclusion) (links | edit)
- Glycogen storage disease type II (transclusion) (links | edit)
- Phosphofructokinase deficiency (transclusion) (links | edit)
- Pyruvate kinase deficiency (transclusion) (links | edit)
- Inborn errors of metabolism (transclusion) (links | edit)
- Glycogen storage disease type I (transclusion) (links | edit)
- Transketolase (transclusion) (links | edit)
- Glycogen storage disease type IV (transclusion) (links | edit)
- Glycogen storage disease type III (transclusion) (links | edit)
- Glycogen storage disease type 0 (transclusion) (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (transclusion) (links | edit)
- Pyruvate carboxylase deficiency (transclusion) (links | edit)
- Hyperoxaluria (transclusion) (links | edit)
- Sucrose intolerance (transclusion) (links | edit)
- Triosephosphate isomerase deficiency (transclusion) (links | edit)
- Galactokinase deficiency (transclusion) (links | edit)
- Aldolase A deficiency (transclusion) (links | edit)
- Glycogen storage disease type VI (transclusion) (links | edit)
- Renal glycosuria (transclusion) (links | edit)
- Pentosuria (transclusion) (links | edit)
- Galactose epimerase deficiency (transclusion) (links | edit)
- Essential fructosuria (transclusion) (links | edit)
- Galactose-1-phosphate uridylyltransferase deficiency (transclusion) (links | edit)
- Glucose-galactose malabsorption (transclusion) (links | edit)
- Mitochondrial pyruvate carrier 2 (transclusion) (links | edit)
- Monocarboxylate transporter 1 (transclusion) (links | edit)
- Primary hyperoxaluria (transclusion) (links | edit)
- Hexokinase deficiency (transclusion) (links | edit)
- Galactosemic cataract (transclusion) (links | edit)
- Glycogen storage disease type IX (transclusion) (links | edit)
- Inborn errors of carbohydrate metabolism (transclusion) (links | edit)
- 6-phosphogluconate dehydrogenase deficiency (transclusion) (links | edit)
- Transaldolase deficiency (transclusion) (links | edit)
- Danon disease (transclusion) (links | edit)
- Metabolic myopathy (transclusion) (links | edit)
- Enolase deficiency (transclusion) (links | edit)
- MODY 2 (transclusion) (links | edit)