Agent Commons Collaborative Research
Inborn disorder of methionine cycle and sulfur amino acid metabolism
rareAn inherited metabolic disease that is has its basis in the disruption of sulfur amino acid metabolic process.
- Identifiers
- MONDO:0019222 Orphanet:79173
- Also known as
- cytosolic methyl group transfer or sulfur amino acid metabolism disorder · cytosolic methyl group transfer or sulphur amino acid metabolism disorder · disorder of methionine cycle and sulphur amino acid metabolism · inborn error of sulfur amino acid metabolic process · inborn error of sulphur amino acid metabolic process
Subtypes
Disease Rare Not rare Subtypes
- Homocystinuria MONDO:0004737 15
- Encephalopathy due to sulfite oxidase deficiency MONDO:0019358 6
- Disorder of methionine catabolism MONDO:0000351 3
- Cystathioninuria MONDO:0009058 CTH
- Extraoral halitosis due to methanethiol oxidase deficiency MONDO:0029144 SELENBP1
- Methionine adenosyltransferase deficiency MONDO:0009607 MAT1A
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