Catalog
Genetic disorders of amino acid metabolism or transport affecting the skin
No MMS code
Link to WHO Definition
Genetic disorders of amino acid metabolism or transport affecting the skin – http://id.who.int/icd/entity/1179082745
Parents
Children
- Multiple carboxylase deficiency
- 5C50.F0 Prolidase deficiency
- Classical homocystinuria
- Propionic aciduria
- 5C50.D0 Maple-syrup-urine disease
- Glutaric aciduria type 1
- 5C50.10 Alkaptonuria
- 5C50.12 Tyrosinaemia type 2
- 5C50.00 Classical phenylketonuria
- Methylmalonic aciduria
- Aspartylglucosaminuria
- 5C50.20 Histidinaemia
- 5C50.A0 Argininosuccinic aciduria
- 5C50.A3 Citrullinaemia
- Hartnup syndrome