Congenital disorders of amino acid metabolism
From Wikipedia - Reading time: 4 min
| Congenital disorders of amino acid metabolism | |
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| The general structure of an α-amino acid, with the amino group on the left and the carboxyl group on the right | |
| Specialty | Endocrinology  |
Inborn errors of amino acid metabolism are metabolic disorders which impair the synthesis and degradation of amino acids.
Types[edit]
- Alkaptonuria
- Aspartylglucosaminuria
- Branched-chain keto acid dehydrogenase kinase deficiency
- 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
- Hypermethioninemia
- Hyperlysinemias
- Nonketotic hyperglycinemia
- Propionic acidemia
- Hyperprolinemia
Amino acid transport disorders[edit]
Amino acid storage disorders[edit]
References[edit]
External links[edit]
 | This article about an endocrine, nutritional, or metabolic disease is a stub. You can help Wikipedia by expanding it. |
Licensed under CC BY-SA 3.0 | Source: https://en.wikipedia.org/wiki/Congenital_disorders_of_amino_acid_metabolism1 | ↧ Download as ZWI file
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