Congenital disorders of amino acid metabolism
Inborn errors of amino acid metabolism are metabolic disorders which impair the synthesis and degradation of amino acids.
| Congenital disorders of amino acid metabolism | |
|---|---|
 | |
| The general structure of an α-amino acid, with the amino group on the left and the carboxyl group on the right. | |
| Specialty | Endocrinology  |
Types
- 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
- Hypermethioninemia
- Hyperlysinemias
- Nonketotic hyperglycinemia
- Propionic acidemia
- Hyperprolinemia
Amino acid transport disorders
Amino acid storage disorders
gollark: Assuming that you add no safety or error correction whatsoever.
gollark: I guess if you want to send strings across TIS-3D infrared networks, you could with careful design probably get 4 bits/tick then, which is not entirely awful.
gollark: TIS-3D can internally store values between -32768 and 32767. That's, er, two bytes.
gollark: Redstone allows 4 bits (0-15) per toggling. Can those take a tick? No idea.
gollark: Well, you're wasting 15/16ths of the bandwidth, then.
References
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