Begreppsinformation
Föredragen term
Metabolism, Inborn Errors
Typ
-
Topical Descriptor
Överordnat begrepp
Underordnade begrepp
- Amino Acid Metabolism, Inborn Errors
- Amino Acid Transport Disorders, Inborn
- Amyloidosis, Familial
- Brain Diseases, Metabolic, Inborn
- Carbohydrate Metabolism, Inborn Errors
- Cytochrome-c Oxidase Deficiency
- Hyperbilirubinemia, Hereditary
- Lipid Metabolism, Inborn Errors
- Lysosomal Storage Diseases
- Metal Metabolism, Inborn Errors
- Peroxisomal Disorders
- Progeria
- Purine-Pyrimidine Metabolism, Inborn Errors
- Renal Tubular Transport, Inborn Errors
- Steroid Metabolism, Inborn Errors
Hänvisningstermer
- Error, Inborn Metabolism
- Errors, Inborn Metabolism
- Inborn Errors of Metabolism
- Inborn Metabolism Error
- Inborn Metabolism Errors
- Metabolism Error, Inborn
- Metabolism Errors, Inborn
- Metabolism Inborn Error
- Metabolism Inborn Errors
Anmärkning
- general or unspecified; prefer specific types; differentiate from DEFICIENCY DISEASES
Användningsanmärkning
- Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero.
Anmärkning om ändringshistoria
- 65
Termer på andra språk
-
finska
-
synnynnäinen aineenvaihduntahäiriö
-
synnynnäinen metabolinen häiriö
-
synnynnäiset metaboliset häiriöt
-
svenska
URI
http://www.yso.fi/onto/mesh/D008661
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