Pages that link to "Galactosemia"
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Showing 217 items.
- Allele (links | edit)
- Genetic disorder (links | edit)
- Glucose (links | edit)
- Fructose (links | edit)
- Sucrose (links | edit)
- Galactose (links | edit)
- Lactose intolerance (links | edit)
- List of genetic disorders (links | edit)
- Infant formula (links | edit)
- Neonatal heel prick (links | edit)
- Cataract (links | edit)
- Irish Travellers (links | edit)
- Glycogen storage disease type V (links | edit)
- Glycogen storage disease (links | edit)
- Congenital disorder of glycosylation (links | edit)
- List of diseases (G) (links | edit)
- Genetic counseling (links | edit)
- Blood sugar level (links | edit)
- Fructose bisphosphatase deficiency (links | edit)
- Glucose-6-phosphate dehydrogenase deficiency (links | edit)
- Carbohydrate metabolism (links | edit)
- Luis Federico Leloir (links | edit)
- Galactosemia (transclusion) (links | edit)
- Phosphoglucomutase (links | edit)
- Transferase (links | edit)
- Galactokinase (links | edit)
- Budd–Chiari syndrome (links | edit)
- Biliary atresia (links | edit)
- Fructose malabsorption (links | edit)
- Hereditary fructose intolerance (links | edit)
- Newborn screening (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)
- List of systemic diseases with ocular manifestations (links | edit)
- Lactulose (links | edit)
- Human genetics (links | edit)
- Galactose-1-phosphate uridylyltransferase (links | edit)
- Glycogen storage disease type I (links | edit)
- Reactive hypoglycemia (links | edit)
- Neonatal jaundice (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)
- Galactosaemia (redirect page) (links | edit)
- Classical galactosemia (redirect page) (links | edit)
- Crigler–Najjar syndrome (links | edit)
- Chromosome 1 (links | edit)
- Chromosome 9 (links | edit)
- Chromosome 17 (links | edit)
- Medical genetics (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Follicular atresia (links | edit)
- Primary ovarian insufficiency (links | edit)
- Galactosemias (redirect page) (links | edit)
- List of MeSH codes (C18) (links | edit)
- List of MeSH codes (C16) (links | edit)
- List of MeSH codes (C10) (links | edit)
- User:Brainist/MeSH articles (links | edit)
- Neonatal cholestasis (links | edit)
- Classic Galactosemia (redirect page) (links | edit)
- Robert Guthrie (links | edit)
- Fortisip (links | edit)
- Pyruvate carboxylase deficiency (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)
- UTP—glucose-1-phosphate uridylyltransferase (links | edit)
- Renal glycosuria (links | edit)
- Pentosuria (links | edit)
- Galactosemia type 1 (redirect page) (links | edit)
- Galt deficiency (redirect page) (links | edit)
- Galactosemia classic (redirect page) (links | edit)
- Galactose epimerase deficiency (links | edit)
- Galactosemia type 3 (redirect page) (links | edit)
- UDP-Galactose-4-epimerase deficiency (redirect page) (links | edit)
- UDPglucose-4-epimerase deficiency (redirect page) (links | edit)
- UDP-galactose-4-epimerase deficiency (redirect page) (links | edit)
- List of diseases (U) (links | edit)
- User talk:Anandks007/Med (links | edit)
- GALE deficiency (redirect page) (links | edit)
- Galactosaemia III (redirect page) (links | edit)
- Galactosaemia I (redirect page) (links | edit)
- Galactosemia I (redirect page) (links | edit)
- Galactosemia III (redirect page) (links | edit)
- Galactose 1-phosphate (links | edit)
- Essential fructosuria (links | edit)
- Galactose-1-phosphate uridylyltransferase deficiency (links | edit)
- Hypermethioninemia (links | edit)
- Mendelian traits in humans (links | edit)
- Etifoxine (links | edit)
- Glucose-galactose malabsorption (links | edit)
- Breastfeeding difficulties (links | edit)
- UDP-glucose 4-epimerase (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)
- Inborn errors of carbohydrate metabolism (links | edit)
- Galactitol (links | edit)
- Beutler test (links | edit)
- 6-phosphogluconate dehydrogenase deficiency (links | edit)
- Transaldolase deficiency (links | edit)
- Ernest Beutler (links | edit)
- Breastfeeding (links | edit)
- Danon disease (links | edit)
- Metabolic myopathy (links | edit)
- Enolase deficiency (links | edit)
- Cirrhosis (links | edit)
- William J. Rutter (links | edit)
- MODY 2 (links | edit)
- Galactoseamia (redirect page) (links | edit)
- Leloir Institute (links | edit)
- Francine Ratner Kaufman (links | edit)
- List of causes of hypoglycemia (links | edit)
- List of OMIM disorder codes (links | edit)
- Galactolysis (links | edit)
- Fanconi syndrome (links | edit)
- Proximal renal tubular acidosis (links | edit)
- Hypergonadotropic hypogonadism (links | edit)
- Congenital cataract (links | edit)
- Developmental verbal dyspraxia (links | edit)
- Newborn Screening Saves Lives Reauthorization Act of 2013 (links | edit)
- Kurt Julius Isselbacher (links | edit)
- Childhood cataract (links | edit)
- Oligogenic inheritance (links | edit)
- Simple Mendelian genetics in humans (links | edit)
- Adult polyglucosan body disease (links | edit)
- Duarte galactosemia (links | edit)
- Purple sweet potato color (links | edit)
- Galactocemia (redirect page) (links | edit)
- Breastfeeding contraindications (links | edit)
- Friedrich Göppert (links | edit)
- Mitochondrial pyruvate carrier 1 (links | edit)
- Govorestat (links | edit)
- Talk:Galactosemia (transclusion) (links | edit)
- Talk:Esther Lederberg (links | edit)
- Talk:Galactosemic cataract (links | edit)
- Talk:Hemp/Archive 1 (links | edit)
- User:CyborgTosser (links | edit)
- User:Threelovemonkeys/Sandbox (links | edit)
- User:Topbanana/langlinks (links | edit)
- User:Rickremember (links | edit)
- User:Medical geneticist/Sandbox (links | edit)
- User:Madhero88/OthersBM (links | edit)
- User:RussBot/Similar titles report/09 (links | edit)
- User:Davidruben/OrphaNet (links | edit)
- User:Magnus Manske/Genomics articles needing citations (links | edit)
- User:WillPugarth/sandbox (links | edit)
- User:Michelle.am.kidd/sandbox (links | edit)
- User:WeijiBaikeBianji/sandbox13 (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia (links | edit)
- User:Drsalmanshah165/Books/Anaphylaxis (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-G (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia0-h (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-H (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-I (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipediac0-J (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-K (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-L (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-M (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-N (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-O (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-pha (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia0-pln (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-P (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-Q (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-R (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-S (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-T (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-U (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-V (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-W (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-X (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-Y (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-z (links | edit)
- User:Drsalmanshah165/Books/Medical wikipedia (links | edit)
- User:Drsalmanshah165/Books/Offline Medical Wikipedia (links | edit)
- User:Drsalmanshah165/Books/Offline Medical Wikipedia 0-Z (links | edit)
- User:Daniel Mietchen/Wikidata lists/Items with MeSH Codes (links | edit)
- User:Daniel Mietchen/Wikidata lists/Items with Disease Ontology IDs (links | edit)
- User:West.andrew.g/2014 Top Medical Articles (links | edit)
- User:West.andrew.g/Popular medical pages (links | edit)
- User:Xeldarith/sandbox (links | edit)
- User:Lgmarti/sandbox (links | edit)
- User:Gavivz/Books/Inborn errors of metabolism (links | edit)
- User:Michaelzhuchen/sandbox/UTP—glucose-1-phosphate uridylyltransferase (links | edit)
- User:Renjini p a/sandbox (links | edit)
- User:PriceDL/List of all WikiProject Medicine articles (links | edit)
- User:CFCF/sandbox/46 (links | edit)
- User:Canada Hky/NBS (links | edit)
- User:Y-S.Ko/Wikipedia course/Diseases (links | edit)
- User:Drmanish7506/Books/inborn error of metabolism (links | edit)
- User:Mmaguilar2/New Sandbox (links | edit)
- User:Stp20 (links | edit)
- User:Just some student on the web/sandbox (links | edit)
- User:Jay9Z/Follicular atresia (links | edit)
- User:Scranton (links | edit)
- User:Simply28/sandbox (links | edit)
- User:Tigers900/Evaluate an Article (links | edit)
- User talk:170.235.201.26 (links | edit)
- User talk:Hillhcky55 (links | edit)
- User talk:Yehudamalul (links | edit)
- User talk:199.180.150.18 (links | edit)
- User talk:71.40.207.4 (links | edit)
- Wikipedia:Reference desk/Archives/Science/2006 September 28 (links | edit)
- Wikipedia:WikiProject Spam/LinkReports/arup.utah.edu (links | edit)
- Wikipedia:WikiProject Medicine/Lists of pages/Articles (links | edit)
- Wikipedia:WikiProject Medicine/Lists of pages/Low-importance medicine articles (links | edit)
- Wikipedia:WikiProject Medicine/Popular pages En 2013b (links | edit)
- Wikipedia:WikiProject Short descriptions/wd/diseases (links | edit)
- Wikipedia:WikiProject Academic Journals/Journals cited by Wikipedia/N47 (links | edit)
- Wikipedia:WikiProject Medicine/The ICD-11 coding challenge/900–999 (links | edit)
- Template:Inborn errors of carbohydrate metabolism (links | edit)
- Portal:Argentina/Selected article/Month 12, 2007 (links | edit)