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Inborn disorder of aspartate family metabolism
rareAn inherited metabolic disease that is has its basis in the disruption of aspartate family amino acid metabolic process.
- Identifiers
- MONDO:0037938
- Part of
- Inborn errors of metabolism
- Also known as
- inborn aspartate family amino acid metabolic process disorder · inborn error of aspartate family amino acid metabolic process · rare inborn error of aspartate family amino acid metabolic process
Subtypes
| Disease | Subtypes |
|---|---|
| Inborn disorder of lysine and hydroxylysine metabolism | 6 |
| Disorder of methionine catabolism | 3 |
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