Galactosemia
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Galactosemia - Wikipedia, the free encyclopedia
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Galactosemia, Articles with unsourced statements since May 2008, Inborn errors of carbohydrate metabolism, Fructose and galactose metabolism enzymes, Glycolysis enzymes, Pentose phosphate pathway enzymes, Aldehyde, Amino, Ataxia, Brain damage, Cataract" |
Galactosemia - Genetics Home Reference
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galactosemia, Brain Diseases, Metabolic, Inborn, Brain Diseases, Metabolic, Brain Diseases, Central Nervous System Diseases, Nervous System Diseases, Metabolism, Inborn Errors, Genetic Diseases, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Carbohydrate Metabolism, Inborn Errors, Metabolic Diseases, Nutritional and Metabolic Diseases, Galactosemias, Brain and nervous system, Digestive system, Eyes and vision, Food, nutrition, and metabolism, Newborn screening, GALE, GALE gene, GALK1, GALK1 gene, GALT, GALT gene, Classic Galactosemia, Epimerase deficiency galactosemia, Galactokinase Deficiency Disease, Galactose-1-Phosphate Uridyl-Transferase Deficiency Disease, Galactose epimerase deficiency, GALT Deficiency, UDP-Galactose-4-Epimerase Deficiency Disease, UDPglucose 4-Epimerase Deficiency Disease, UDPglucose Hexose-1-Phosphate Uridylyltransferase Deficiency, UTP Hexose-1-Phosphate Uridylyltransferase Deficiency, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems |
eMedicine - Galactose-1-Phosphate Uridyltransferase Deficiency (Galactosemia) : Artic
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Hereditary galactosemia is among the most common carbohydrate metabolism disorders and can be a life-threatening illness galactose-1-phosphate uridyltransferase deficiency, GALT, hypergalactosemia, classic galactosemia, GALT deficiency |