Catalog
Classical organic aciduria
Link to WHO Definition
Classical organic aciduria – http://id.who.int/icd/entity/1879509617
This a term used to classify a group of metabolic disorders which disrupt normal amino acid metabolism, particularly branched-chain amino acids, causing a buildup of acids which are usually not present.
Parents
Children
- 3-methylglutaconic aciduria
- Neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency
- Multiple carboxylase deficiency
- 2-methylbutyric aciduria
- 3-hydroxyisobutyric aciduria
- Isobutyric aciduria
- Propionic aciduria
- Methylmalonate semialdehyde dehydrogenase deficiency
- Isovaleric aciduria
- Methylmalonic aciduria - homocystinuria
- Methylmalonic aciduria
- Ketoacidosis due to beta-ketothiolase deficiency
- Glutaric aciduria type 3
- 3-methylcrotonylglycinuria
- 3-hydroxy-3-methylglutaric aciduria