The following pages link to Hereditary fructose intolerance
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- 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)
- List of diseases (F) (links | edit)
- List of diseases (H) (links | edit)
- Blood sugar level (links | edit)
- Fructose bisphosphatase deficiency (links | edit)
- Glucose-6-phosphate dehydrogenase deficiency (links | edit)
- Galactosemia (links | edit)
- Phosphoglucomutase (links | edit)
- Fructose malabsorption (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)
- Breath test (links | edit)
- Food intolerance (links | edit)
- Glucose/fructose/phosphoric acid (links | edit)
- Hepatomegaly (links | edit)
- Glycogen storage disease type I (links | edit)
- Reactive hypoglycemia (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)
- HFI (links | edit)
- List of MeSH codes (C18) (links | edit)
- List of MeSH codes (C16) (links | edit)
- Neonatal hepatitis (links | edit)
- Alitretinoin (links | edit)
- Pyruvate carboxylase deficiency (links | edit)
- Hyperoxaluria (links | edit)
- Sucrose intolerance (links | edit)
- Triosephosphate isomerase deficiency (links | edit)
- Aldolase B (links | edit)
- Galactokinase deficiency (links | edit)
- Aldolase A deficiency (links | edit)
- Glycogen storage disease type VI (links | edit)
- Fructose-bisphosphate aldolase (links | edit)
- Renal glycosuria (links | edit)
- Pentosuria (links | edit)
- Galactose epimerase deficiency (links | edit)
- Fructose 1-phosphate (links | edit)
- Essential fructosuria (links | edit)