Catalog
Disorders of methionine cycle or sulphur amino acid metabolism
Link to WHO Definition
Disorders of methionine cycle or sulphur amino acid metabolism – http://id.who.int/icd/entity/67872354
Parents
Children
- Methionine malabsorption syndrome
- Hypermethioninaemia due to adenosine kinase deficiency
- Homocystinaemia
- Beery-baby syndrome
- Hepatic methionine adenosyltransferase deficiency
- Cystathioninuria
- Hypermethioninaemia
- Classical homocystinuria
- Glycine N-methyltransferase deficiency
- Deficiency of homoserine deaminase
- Secondary non-genetic disorders of methionine cycle or sulfur amino acid metabolism
- Cystathioninemia
- Other genetic defects of methionine cycle or sulfur amino acid metabolism
- Deficiency of methionine adenosyltransferase
- Psychomotor retardation and myopathy due to S-adenosylhomocysteine hydrolase deficiency
- Deficiency of cystathionase
- Brain demyelination due to methionine adenosyltransferase deficiency
- Encephalopathy due to sulfite oxidase deficiency
- Deficiency of cysteine desulfhydrase
- Homocystinuria without methylmalonic aciduria
- Sulfite oxidase deficiency
- Hereditary megaloblastic anaemia due to transcobalamin deficiency
- Familial methionine malabsorption