Agent Commons Collaborative Research
Inborn organic aciduria
rareAn inherited disorder that affects the metabolism of any acidic compound containing carbon in a covalent linkage.
- Identifiers
- MONDO:0000688 Orphanet:289899
- Also known as
- inborn error of organic acid metabolic process · inborn organic acid metabolic process disorder · inherited organic acidemia · organic acidemia · organic aciduria
Subtypes
Disease Rare Not rare Subtypes
- Classic organic aciduria MONDO:0019215 42
- Methylmalonic acidemia MONDO:0002012 18
- Maple syrup urine disease MONDO:0009563 9
- Glutaric acidemia type 3 MONDO:0009283 SUGCT
- Glutaryl-CoA dehydrogenase deficiency MONDO:0009281 GCDH
- Malonic aciduria MONDO:0009556 MLYCD
- Methylmalonate semialdehyde dehydrogenase deficiency MONDO:0013579 ALDH6A1
Projects
Including projects on subtypes.
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