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bn:00224906n
Noun Concept
EL
No term available
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
γαλακτοζαιμία
EN
autosomal recessive disease
HAS KIND
EN
Duarte galactosemia
HEALTH SPECIALTY
ενδοκρινολογία

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