Pages that link to "Fanconi–Bickel syndrome"
Showing 18 items.
- Glycogen storage disease (links | edit)
- List of diseases (F) (links | edit)
- Guido Fanconi (links | edit)
- Glucose transporter (links | edit)
- Inborn errors of carbohydrate metabolism (links | edit)
- Glycogen storage disease type 11 (redirect page) (links | edit)
- Glycogenosis type 11 (redirect page) (links | edit)
- Pseudo-phlorizin diabetes (redirect page) (links | edit)
- Bickel-Fanconi syndrome (redirect page) (links | edit)
- Bickel Fanconi glycogenosis (redirect page) (links | edit)
- Fanconi Bickel syndrome (redirect page) (links | edit)
- List of OMIM disorder codes (links | edit)
- Fanconi-Bickel syndrome (redirect page) (links | edit)
- Genetic disorder (links | edit)
- Glucose (links | edit)
- Fructose (links | edit)
- Sucrose (links | edit)
- Lactose intolerance (links | edit)
- Crohn's disease (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)
- Cotransporter (links | edit)
- Cystinuria (links | edit)
- Phosphofructokinase deficiency (links | edit)
- Pyruvate kinase deficiency (links | edit)
- Inborn errors of metabolism (links | edit)
- Pendred syndrome (links | edit)
- Diastrophic dysplasia (links | edit)
- Atelosteogenesis, type II (links | edit)
- Fuchs' dystrophy (links | edit)
- Glycogen storage disease type I (links | edit)
- Gitelman syndrome (links | edit)
- Hartnup disease (links | edit)
- Salla disease (links | edit)
- Lysinuric protein intolerance (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)
- 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)
- Pyruvate carboxylase deficiency (links | edit)
- Multiple epiphyseal dysplasia (links | edit)
- Hyperoxaluria (links | edit)
- Sucrose intolerance (links | edit)
- Episodic ataxia (links | edit)
- Triosephosphate isomerase deficiency (links | edit)
- Thyroid dyshormonogenesis (links | edit)
- Galactokinase deficiency (links | edit)
- Aldolase A deficiency (links | edit)
- Glycogen storage disease type VI (links | edit)
- Arterial tortuosity syndrome (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)
- Allan–Herndon–Dudley syndrome (links | edit)
- GLUT1 deficiency (links | edit)
- Glucose-galactose malabsorption (links | edit)
- Major facilitator superfamily (links | edit)
- Mitochondrial pyruvate carrier 2 (links | edit)
- Monocarboxylate transporter 1 (links | edit)
- Primary hyperoxaluria (links | edit)
- Hexokinase deficiency (links | edit)
- Galactosemic cataract (links | edit)
- Glycogen storage disease type IX (links | edit)
- Fanconi–Bickel syndrome (links | edit)
- Inborn errors of carbohydrate metabolism (links | edit)
- 6-phosphogluconate dehydrogenase deficiency (links | edit)
- Transaldolase deficiency (links | edit)
- Danon disease (links | edit)
- Metabolic myopathy (links | edit)
- Enolase deficiency (links | edit)
- Iminoglycinuria (links | edit)
- MODY 2 (links | edit)
- Ichthyosis prematurity syndrome (links | edit)
- Congenital disorder of glycosylation type IIc (links | edit)
- SLC17A3 (links | edit)
- Adult polyglucosan body disease (links | edit)
- Mitochondrial pyruvate carrier 1 (links | edit)
- SPATCCM (links | edit)
- User:Madhero88/OthersBM (links | edit)
- User:Michelle.am.kidd/sandbox (links | edit)
- User:Lgmarti/sandbox (links | edit)
- User:Y-S.Ko/Wikipedia course/Diseases (links | edit)
- User:Just some student on the web/sandbox (links | edit)
- Template:Inborn errors of carbohydrate metabolism (links | edit)
- Template:Solute carrier disorders (links | edit)
- Glut2 deficiency (redirect page) (links | edit)
- Talk:Fanconi–Bickel syndrome (transclusion) (links | edit)
- Wikipedia:WikiProject Medicine/Lists of pages/Articles (links | edit)
- Wikipedia:WikiProject Academic Journals/Journals cited by Wikipedia/H12 (links | edit)
- Wikipedia:WikiProject Medicine/The ICD-11 coding challenge/4400–4499 (links | edit)