Carbohydrate Metabolism, Inborn Errors

Dysfunctions of CARBOHYDRATE METABOLISM resulting from inborn genetic mutations that are inherited or acquired in utero.

Year introduced: 1965

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C16.320.565.202, C18.452.648.202

MeSH Unique ID: D002239

Entry Terms:

• Carbohydrate Metabolism, Inborn Error

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
Fructose Metabolism, Inborn Errors
Fructose-1,6-Diphosphatase Deficiency
Fructose Intolerance
Fucosidosis
Galactosemias
Glucosephosphate Dehydrogenase Deficiency
Glycogen Storage Disease
Glycogen Storage Disease Type I
Glycogen Storage Disease Type II
Glycogen Storage Disease Type IIb
Glycogen Storage Disease Type III
Glycogen Storage Disease Type IV
Glycogen Storage Disease Type V
Glycogen Storage Disease Type VI
Glycogen Storage Disease Type VII
Glycogen Storage Disease Type VIII
Hyperoxaluria, Primary
Lactose Intolerance
Mannosidase Deficiency Diseases
alpha-Mannosidosis
beta-Mannosidosis
Mucolipidoses
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis II
Mucopolysaccharidosis III
Mucopolysaccharidosis IV
Mucopolysaccharidosis VI
Mucopolysaccharidosis VII
Multiple Carboxylase Deficiency
Biotinidase Deficiency
Holocarboxylase Synthetase Deficiency
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease

All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Congenital Disorders of Glycosylation
Fructose Metabolism, Inborn Errors
Fructose-1,6-Diphosphatase Deficiency
Fructose Intolerance
Fucosidosis
Galactosemias
Glucosephosphate Dehydrogenase Deficiency
Glycogen Storage Disease
Glycogen Storage Disease Type I
Glycogen Storage Disease Type II
Glycogen Storage Disease Type IIb
Glycogen Storage Disease Type III
Glycogen Storage Disease Type IV
Glycogen Storage Disease Type V
Glycogen Storage Disease Type VI
Glycogen Storage Disease Type VII
Glycogen Storage Disease Type VIII
Hyperoxaluria, Primary
Lactose Intolerance
Mannosidase Deficiency Diseases
alpha-Mannosidosis
beta-Mannosidosis
Mucolipidoses
Mucopolysaccharidoses
Mucopolysaccharidosis I
Mucopolysaccharidosis II
Mucopolysaccharidosis III
Mucopolysaccharidosis IV
Mucopolysaccharidosis VI
Mucopolysaccharidosis VII
Multiple Carboxylase Deficiency
Biotinidase Deficiency
Holocarboxylase Synthetase Deficiency
Pyruvate Metabolism, Inborn Errors
Leigh Disease
Pyruvate Carboxylase Deficiency Disease
Pyruvate Dehydrogenase Complex Deficiency Disease