Disorder of methionine catabolism

MONDO:0000351

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

Also known as: hypermethioninemia, inborn error of methionine catabolic process, inborn methionine catabolic process disorder, rare inborn error of methionine catabolic process

1 clinical trial for this condition and its sub-types, 0 tagged with Disorder of methionine catabolism itself.

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Part of

↑ Inborn disorder of amino acid metabolism (159) ↑ Inborn disorder of methionine cycle and sulfur amino acid metabolism (11) ↑ Inborn disorder of aspartate family metabolism (0)

Sub-types of Disorder of methionine catabolism

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

Including sub-types (1) Tagged with Disorder of methionine catabolism (0)

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