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... > 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
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Glycogen Storage Disease > Glycogen Storage Disease Type VI

Término preferido

Glycogen Storage Disease Type VI  

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Tipo

  • mesh:Descriptor

Definición

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

Concepto genérico

Conceptos relacionados

Etiquetas alternativas

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

En otras lenguas

  • Glycogénose de type VI

    francés

  • Déficit en phosphorylase hépatique
  • Glycogénose de type 6
  • Glycogénose de type 6b
  • Glycogénose de type VIb
  • Maladie de Hers

URI

http://data.loterre.fr/ark:/67375/JVR-KWXWQ09G-8

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