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Concept information

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Congenital Disorders of Glycosylation
Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Carbohydrate Metabolism, Inborn Errors > Congenital Disorders of Glycosylation

Preferred term

Congenital Disorders of Glycosylation  

Type

  • mesh:Descriptor

Definition

  • A genetically heterogeneous group of heritable disorders resulting from defects in protein N-glycosylation.

Broader concept

Entry terms

  • Carbohydrate-Deficient Glycoprotein Syndrome
  • Glycoprotein Syndrome, Carbohydrate-Deficient

Allowable Qualifier(s)

In other languages

  • Troubles congénitaux de la glycosylation

    French

  • Anomalies congénitales de la glycosylation
  • CDG (Congenital Disorders of Glycosylation)
  • Syndrome CDG
  • Syndrome des glycoprotéines déficientes en hydrates de carbone
  • TCG (Troubles Congénitaux de la Glycosylation)
  • Trouble congénital de la glycosylation

URI

http://data.loterre.fr/ark:/67375/JVR-Q5VPBZ11-F

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RDF/XML TURTLE JSON-LD Created 5/24/95, last modified 6/25/10