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bn:00139968n
Noun Concept
Categories: Inborn errors of carbohydrate metabolism, Autosomal recessive disorders
EN
galactokinase deficiency  Galactosaemia II  Galactosemia II  Galactosemia type 2  GALK deficiency
EN
Galactokinase deficiency is an autosomal recessive metabolic disorder marked by an accumulation of galactose and galactitol secondary to the decreased conversion of galactose to galactose-1-phosphate by galactokinase. Wikipedia
Definitions
Relations
Sources
EN
Galactokinase deficiency is an autosomal recessive metabolic disorder marked by an accumulation of galactose and galactitol secondary to the decreased conversion of galactose to galactose-1-phosphate by galactokinase. Wikipedia
Galactosemia that involves an accumulation of galactose and galactitol secondary to the decreased conversion of galactose to galactose-1-phosphate by galactokinase Wikidata
IS A
disease
rare disease
galactosemia
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
galactokinase deficiency
Wikidata
EN
galactokinase deficiency
Wikipedia Redirections
EN
Galactosaemia II, Galactosemia II, Galactosemia type 2, GALK deficiency
Wikidata Alias
EN
Galactosemia II

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