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Disease Carbohydrate Metabolism, Inborn Errors

Name Carbohydrate Metabolism, Inborn Errors
Synonym Carbohydrate Metabolism, Inborn Error
Definition Dysfunctions of CARBOHYDRATE METABOLISM resulting from inborn genetic mutations that are inherited or acquired in utero.
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID D002239
External Links

Top ↑ Ancestors

1. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Carbohydrate Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references
2. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references Has associated exposure references Carbohydrate Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references

Top ↑ Descendants

Carbohydrate Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references
  Chondroitin-6-Sulfaturia, Defective Cellular Immunity, Nephrotic Syndrome
View node Congenital Disorders of Glycosylation Has associated chemicals Has associated genes Has associated phenotype references
  D-glycericacidemia Has associated chemicals Has associated genes Has associated phenotype references
  Fructose and Galactose Intolerance
View node Fructose Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references
  Fucosidosis Has associated chemicals Has associated genes Has associated phenotype references
  Glucose-Galactose Malabsorption Has associated chemicals Has associated genes Has associated phenotype references
View node Glucosephosphate Dehydrogenase Deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Glut1 Deficiency Syndrome Has associated chemicals Has associated genes Has associated phenotype references
  GLYCEROL KINASE DEFICIENCY Has associated chemicals Has associated genes Has associated phenotype references
View node Glycogen Storage Disease Has associated chemicals Has associated genes Has associated phenotype references
View node Hyperoxaluria, Primary Has associated chemicals Has associated genes Has associated phenotype references
  Hyperproglucagonemia
  Lactase Deficiency, Congenital Has associated chemicals Has associated genes Has associated phenotype references
  Lactate Dehydrogenase Deficiency
View node Lactose Intolerance Has associated chemicals Has associated genes Has associated phenotype references
View node Mannosidase Deficiency Diseases Has associated chemicals Has associated genes Has associated phenotype references
View node Mucolipidoses Has associated chemicals Has associated genes Has associated phenotype references
View node Mucopolysaccharidoses Has associated chemicals Has associated genes Has associated phenotype references
View node Multiple Carboxylase Deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Myopathy with Storage of Glycoproteins and Glycosaminoglycans
  Pentosuria Has associated chemicals Has associated genes Has associated phenotype references
  Phosphoenolpyruvate carboxykinase deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Phosphoenolpyruvate Carboxykinase Deficiency, Mitochondrial
  Phosphoglycerate Dehydrogenase Deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Polysaccharide, Storage of Unusual
View node Pyruvate Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated phenotype references
  Ribose 5-Phosphate Isomerase Deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Sucrase-isomaltase deficiency, congenital Has associated chemicals Has associated genes Has associated phenotype references
  Transaldolase Deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Trehalase Deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Triosephosphate Isomerase Deficiency Has associated chemicals Has associated genes Has associated phenotype references
  Galactosemias Has associated chemicals Has associated genes Has associated phenotype references
  Xylosidase Deficiency