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... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Glycogen Storage Disease > Glycogen Storage Disease Type VI
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Glycogen Storage Disease > Glycogen Storage Disease Type VI

Preferred term

Glycogen Storage Disease Type VI  

Type

  • Topical Descriptor

Broader concept

Related concepts

Entry terms

  • Disease, Hers
  • Disease, Hers'
  • Glycogenosis 6
  • Glycogenosis Type VI
  • Glycogenosis VI
  • Hepatic Glycogen Phosphorylase Deficiency
  • Her Disease
  • Hers Disease
  • Hers' Disease
  • Liver Phosphorylase Deficiency Syndrome
  • Type VI, Glycogenosis

Scope note

  • A hepatic GLYCOGEN STORAGE DISEASE in which there is an apparent deficiency of hepatic phosphorylase (GLYCOGEN PHOSPHORYLASE, LIVER FORM) activity.

History note

  • 91(89); was see under GLYCOGEN STORAGE DISEASE 1989-90; was GLYCOGENOSIS 6 see under GLYCOGENOSIS 1975-88

In other languages

  • glykogenoosi VI

    Finnish

  • dekstrinoosi tyyppi VI
  • dekstrinoosi VI
  • glykogenoosi tyyppi VI
  • Hers
  • Hersin tauti
  • morbus Hers
  • tyypin VI dekstrinoosi
  • tyypin VI glykogenoosi
  • tyyppi VI dekstrinoosi
  • tyyppi VI glykogenoosi
  • Glykogeninlagringssjukdom typ VI

    Swedish

  • Glykogenos 6
  • Glykogenos typ VI
  • Hers sjukdom

URI

http://www.yso.fi/onto/mesh/D006013

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