Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Carbohydrate Metabolism, Inborn Errors
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Carbohydrate Metabolism, Inborn Errors
Description
Dysfunctions of CARBOHYDRATE METABOLISM resulting from inborn genetic mutations that are inherited or acquired in utero. MeSH
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Subtype Terms (13)
Congenital Disorders of Glycosylation
7 drugs (2 approved, 5 experimental)
Fructose Metabolism, Inborn Errors
Fucosidosis
11 drugs (8 approved, 3 experimental)
Galactosemias
4 drugs (3 approved, 1 experimental)
Glucosephosphate Dehydrogenase Deficiency
12 drugs (5 approved, 7 experimental)
Glycogen Storage Disease
7 drugs (2 approved, 5 experimental)
Hyperoxaluria, Primary
6 drugs (3 approved, 3 experimental)
Lactose Intolerance
21 drugs (3 approved, 18 experimental)
Mannosidase Deficiency Diseases
5 drugs (4 approved, 1 experimental)
Mucolipidoses
7 drugs (6 approved, 1 experimental)
Mucopolysaccharidoses
39 drugs (19 approved, 20 experimental)
Approved Indicated Drugs (1)
Other Experimental Indicated Drugs (1)
Organization Involved with Phase 4 Indications (1)
Organization Involved with Phase 3 Indications (1)
Organization Involved with Phase 2 Indications (1)
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UMLS Data
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