The following pages link to Glycogen storage disease type I
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Glucose (links | edit)
- Hypoglycemia (links | edit)
- Human genome (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)
- Fructose bisphosphatase deficiency (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)
- Otto von Gierke (links | edit)
- Gierke (links | edit)
- Von Gierke's Disease (redirect page) (links | edit)
- Von Gierke disease (redirect page) (links | edit)
- List of diseases (V) (links | edit)
- Glucose-6-phosphate exchanger SLC37A4 (links | edit)
- Medical genetics of Jews (links | edit)
- User:Cyborg Ninja/sandbox (links | edit)
- User:Baileypatricia/draft article on G6PT (links | edit)
- User talk:Anandks007/Med (links | edit)
- Misplaced Pages:WikiProject Resource Exchange/Resource Request/Archive 87 (links | edit)
- Glucose-6-phosphatase deficiency (redirect page) (links | edit)
- Lactic acidosis (links | edit)
- Transketolase (links | edit)
- Glycogen storage disease type IV (links | edit)
- Von Gierke's disease (redirect page) (links | edit)
- Genetic disorder (links | edit)
- Crohn's disease (links | edit)
- Glycogen storage disease (links | edit)
- Congenital disorder of glycosylation (links | edit)
- List of eponymous diseases (links | edit)
- Fructose malabsorption (links | edit)
- Hyperinsulinemic hypoglycemia (links | edit)
- Cystinuria (links | edit)
- Pendred syndrome (links | edit)
- Diastrophic dysplasia (links | edit)
- Atelosteogenesis, type II (links | edit)
- Fuchs' dystrophy (links | edit)
- Gitelman syndrome (links | edit)
- Hartnup disease (links | edit)
- Salla disease (links | edit)
- Lysinuric protein intolerance (links | edit)
- Hereditary elliptocytosis (links | edit)
- Achondrogenesis type 1B (links | edit)
- African iron overload (links | edit)
- Nonsyndromic deafness (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Autosomal recessive multiple epiphyseal dysplasia (links | edit)
- Acrodermatitis enteropathica (links | edit)
- Testicular microlithiasis (links | edit)
- Solute carrier family (links | edit)
- Multiple epiphyseal dysplasia (links | edit)
- Episodic ataxia (links | edit)
- Thyroid dyshormonogenesis (links | edit)
- Arterial tortuosity syndrome (links | edit)
- Renal glycosuria (links | edit)
- Allan–Herndon–Dudley syndrome (links | edit)
- GLUT1 deficiency (links | edit)
- Glucose-galactose malabsorption (links | edit)
- Mitochondrial pyruvate carrier 2 (links | edit)
- Monocarboxylate transporter 1 (links | edit)
- Fanconi–Bickel syndrome (links | edit)
- Inborn errors of carbohydrate metabolism (links | edit)
- Nuclear receptor coregulators (links | edit)
- Iminoglycinuria (links | edit)
- Ichthyosis prematurity syndrome (links | edit)
- Congenital disorder of glycosylation type IIc (links | edit)
- SLC17A3 (links | edit)
- Mitochondrial pyruvate carrier 1 (links | edit)
- SPATCCM (links | edit)
- Template:Solute carrier disorders (links | edit)
- Glycogen storage disease type III (links | edit)
- Glycogen storage disease type 0 (links | edit)
- GSD type I (redirect page) (links | edit)
- Glucose 6-phosphatase (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Glycogen storage disease type 1B (redirect page) (links | edit)
- Glycogen storage disease type i (redirect page) (links | edit)
- List of MeSH codes (C18) (links | edit)
- List of MeSH codes (C16) (links | edit)
- Pyruvate carboxylase deficiency (links | edit)
- Glucose cycle (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)