Congenital Disorders of Glycosylation

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

Year introduced: 2011(1996)

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Tree Number(s): C16.320.565.202.125, C18.452.648.202.125

MeSH Unique ID: D018981

Entry Terms:

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

Previous Indexing:

• Carbohydrate Metabolism, Inborn Errors (1991-1995)
• Glycoproteins (1977-1995)

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Congenital Disorders of Glycosylation

All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Congenital Disorders of Glycosylation