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bn:00221027n
Noun Concept
Categories: Autosomal recessive disorders, Rare diseases
EN
galactose epimerase deficiency  epimerase deficiency  Type III galactosemia  UDPglucose 4-epimerase deficiency disease  Uridine diphosphate galactose-4-epimerase deficiency
EN
Galactose epimerase deficiency, also known as GALE deficiency, Galactosemia III and UDP-galactose-4-epimerase deficiency, is a rare, autosomal recessive form of galactosemia associated with a deficiency of the enzyme galactose epimerase. Wikipedia
Definitions
Relations
Sources
EN
Galactose epimerase deficiency, also known as GALE deficiency, Galactosemia III and UDP-galactose-4-epimerase deficiency, is a rare, autosomal recessive form of galactosemia associated with a deficiency of the enzyme galactose epimerase. Wikipedia
human disease Wikidata
IS A
disease
galactosemia
autosomal recessive disease
Wikipedia
EN
galactose epimerase deficiency
Wikidata
EN
Galactose epimerase deficiency
Wikipedia Redirections
EN
epimerase deficiency
Wikidata Alias
EN
galactose epimerase deficiency, Type III galactosemia, UDPglucose 4-epimerase deficiency disease, Uridine diphosphate galactose-4-epimerase deficiency

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