|
1 / 1
|
DeCS
|
|
 |
|
Descriptor English:
|
|
Fructose Metabolism, Inborn Errors
|
|
Descriptor Spanish:
|
|
Errores Innatos del Metabolismo de la Fructosa
|
|
Descriptor Portuguese:
|
|
Erros Inatos do Metabolismo da Frutose
|
|
Tree Number:
|
|
C16.320.565.202.251
C18.452.648.202.251
|
|
Definition English:
|
|
Inherited abnormalities of fructose metabolism, which include three known autosomal recessive types: hepatic fructokinase deficiency (essential fructosuria), hereditary fructose intolerance, and hereditary fructose-1,6-diphosphatase deficiency. Essential fructosuria is a benign asymptomatic metabolic disorder caused by deficiency in fructokinase, leading to decreased conversion of fructose to fructose-1-phosphate and alimentary hyperfructosemia, but with no clinical dysfunction; may produce a false-positive diabetes test. |
|
History Note English:
|
|
89; FRUCTOSE INTOLERANCE was see under CARBOHYDRATE METABOLISM, INBORN ERRORS 1967-88 (Prov 1964-66)
|
|
Allowable Qualifiers English:
|
|
|
|
Record Number:
|
|
23637
|
|
Unique Identifier:
|
|
D015318
|
Occurrence in VHL:
|
|
|
Similar:
|
|
DeCS
|