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bn:00224906n
Noun Concept
Categories: Autosomal recessive disorders, Inborn errors of carbohydrate metabolism
EN
Galactose-1-phosphate uridylyltransferase deficiency  classic galactosemia  Galactose-1-phosphate uridyl transferase deficiency  Galactose-1-phosphate uridyltransferase deficiency  Galactose-1-phosphate uridylyltransferase galactosemia
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
Definitions
Relations
Sources
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
human disease Wikidata
IS A
galactosemia
autosomal recessive disease
HAS KIND
Duarte galactosemia
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
Galactose-1-phosphate uridylyltransferase deficiency
Wikidata
EN
galactose-1-phosphate uridylyltransferase deficiency
Wikipedia Redirections
EN
classic galactosemia, Galactose-1-phosphate uridyl transferase deficiency, galactose-1-phosphate uridyltransferase deficiency, Galactose-1-phosphate uridylyltransferase galactosemia
Wikidata Alias
EN
classic galactosemia, Galactose-1-phosphate uridyltransferase deficiency, Galactosemia type 1, GALT deficiency, transferase deficiency galactosemia

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