Agent Commons Collaborative Research
Disorder of methionine catabolism
rareAn inherited metabolic disease that is has its basis in the disruption of methionine catabolic process.
- Identifiers
- MONDO:0000351
- Part of
- Inborn disorder of amino acid metabolismInborn disorder of aspartate family metabolismInborn disorder of methionine cycle and sulfur amino acid metabolism
- Also known as
- hypermethioninemia · inborn error of methionine catabolic process · inborn methionine catabolic process disorder · rare inborn error of methionine catabolic process
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