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Up to: Inborn disorder of amino acid metabolism · Inborn disorder of methionine cycle and sulfur amino acid metabolism · Inborn disorder of aspartate family metabolism

Disorder of methionine catabolism

An inherited metabolic disease that is has its basis in the disruption of methionine catabolic process.

0 trials tagged with this condition →

  • Adenosine kinase deficiency 0 trials
  • Glycine N-methyltransferase deficiency 0 trials
  • Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase 0 trials

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