Inborn errors of amino acid metabolism
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| Inborn errors of amino acid metabolism | |
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| Classification and external resources | |
 The general structure of an α-amino acid, with the amino group on the left and the carboxyl group on the right. |
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| ICD-10 | E70-E72 |
| ICD-9 | 270 |
| MeSH | D000592 |
Inborn errors of amino acid metabolism are metabolic disorders which impair the synthesis and degradation of amino acids.
Types include:
- Alkaptonuria
- Aspartylglucosaminuria
- Methylmalonic acidemia
- Maple syrup urine disease
- Homocystinuria
- Tyrosinemia
- Trimethylaminuria
- Hartnup disease
- Biotinidase deficiency
- Ornithine carbamoyltransferase deficiency
- Carbamoyl-phosphate synthase I deficiency disease
- Citrullinemia
- Hyperargininemia
- Hyperhomocysteinemia
- Hyperlysinemias
- Nonketotic hyperglycinemia
- Propionic acidemia
- Hyperprolinemia
[edit] Amino acid transport disorders
[edit] Amino acid storage disorders
[edit] External links
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