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bn:00224906n
Noun Concept
FR
galactosémie classique  Déficit en galactose-1-phosphate uridyltransférase  Galactosémie de type 1
EN
Galactose-1-phosphate uridylyltransferase deficiency is the most common type of galactosemia, an inborn error of galactose metabolism, caused by a deficiency of the enzyme galactose-1-phosphate uridylyltransferase. Wikipedia
Relations
Sources
IS A
galactosémie
maladie à transmission autosomique récessive
HAS KIND
galactosémie variante Duarte
HEALTH SPECIALTY
endocrinologie
Wikidata
FR
galactosémie classique
Wikidata Alias
FR
Déficit en galactose-1-phosphate uridyltransférase, Galactosémie de type 1

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