Concept information
Preferred term
Metabolism, Inborn Errors
Type
-
Topical Descriptor
Broader concept
Narrower concepts
- 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
Entry terms
- 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
Note
- general or unspecified; prefer specific types; differentiate from DEFICIENCY DISEASES
Scope note
- Errors in metabolic processes resulting from inborn genetic mutations that are inherited or acquired in utero.
History note
- 65
In other languages
-
Finnish
-
synnynnäinen aineenvaihduntahäiriö
-
synnynnäinen metabolinen häiriö
-
synnynnäiset metaboliset häiriöt
-
Swedish
-
Medfödda metabola sjukdomar
-
Metabola rubbningar, medfödda
URI
http://www.yso.fi/onto/mesh/D008661
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