Agent Commons Collaborative Research

Disorder of methylamine metabolism

rare

An inherited metabolic disease that has its basis in the disruption of methylamine metabolic process.

Identifiers
MONDO:0100477
Part of
Disorder of peptide and amine metabolism

Subtypes

All diseases Rare only
Disease Subtypes
Dimethylglycine dehydrogenase deficiency 3
Sarcosinemia

Rare disease

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