Pages that link to "Glucose-galactose malabsorption"
The following pages link to Glucose-galactose malabsorption:
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Genetic disorder (← links)
- Glucose (← links)
- Fructose (← links)
- Sucrose (← links)
- Lactose intolerance (← links)
- Glycogen storage disease type V (← links)
- Glycogen storage disease (← links)
- Congenital disorder of glycosylation (← links)
- List of diseases (G) (← links)
- Fructose bisphosphatase deficiency (← links)
- Allan–Herndon–Dudley syndrome (← links)
- Hartnup disease (← links)
- Galactosemia (← links)
- Salla disease (← links)
- Lysinuric protein intolerance (← links)
- Fructose malabsorption (← links)
- Hereditary fructose intolerance (← links)
- Pyruvate carboxylase deficiency (← links)
- Glycogen storage disease type IV (← links)
- Glycogen storage disease type III (← links)
- Glycogen storage disease type 0 (← links)
- Hereditary elliptocytosis (← links)
- Achondrogenesis type 1B (← links)
- Multiple epiphyseal dysplasia (← links)
- Hyperinsulinemic hypoglycemia (← links)
- Primary hyperoxaluria (← links)
- Glycogen storage disease type II (← links)
- Cystinuria (← links)
- Phosphofructokinase deficiency (← links)
- Pyruvate kinase deficiency (← links)
- Ichthyosis prematurity syndrome (← links)
- African iron overload (← links)
- Hyperoxaluria (← links)
- Nonsyndromic deafness (← links)
- Inborn error of metabolism (← links)
- ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases (← links)
- Hexokinase deficiency (← links)
- Template:Inborn errors of carbohydrate metabolism (← links)
- Galactosemic cataract (← links)
- Sucrose intolerance (← links)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (← links)
- Glycogen storage disease type XI (← links)
- Episodic ataxia (← links)
- Pendred syndrome (← links)
- Inborn errors of carbohydrate metabolism (← links)
- Diastrophic dysplasia (← links)
- Atelosteogenesis, type II (← links)
- Glucose-galactose malabsorption syndrome (redirect page) (← links)
- Autosomal recessive multiple epiphyseal dysplasia (← links)
- Triosephosphate isomerase deficiency (← links)