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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Where it sits in the disease tree

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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)

Trials to join now! 1

NIH launches major study to unlock secrets of rare bone diseases

Knowledge-focused Recruiting now

This study aims to collect information and bone samples from up to 1,000 people with bone or mineral disorders, such as tumor-induced osteomalacia or familial tumoral calcinosis. Participants receive standard medical evaluations and may provide bone tissue from surgery or a biops…

Sponsor: National Institute of Dental and Craniofacial Research (NIDCR) • Aim: Knowledge-focused

Last updated Sep 18, 2026 00:00 UTC

Disorder of methionine catabolism

Where it sits in the disease tree

NIH launches major study to unlock secrets of rare bone diseases