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Concept information

disease > genetic disease > hereditary disease > glycogenosis > glycogen storage disease type III
disease > enzymopathy > glycogenosis > glycogen storage disease type III

Preferred term

glycogen storage disease type III  

Definition

  • Glycogen storage disease type III is an autosomal recessive metabolic disorder and inborn error of metabolism (specifically of carbohydrates) characterized by a deficiency in glycogen debranching enzymes.It is also known as Cori's disease in honor of the 1947 Nobel laureates Carl Cori and Gerty Cori. (Wikipedia)

Broader concept

In other languages

  • glycogénose de type III

    French

  • glycogénose de type III musculaire
  • maladie de Cori
  • maladie de Cori-Forbes
  • maladie de Forbes

URI

http://data.loterre.fr/ark:/67375/VH8-XG4NPZBJ-T

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