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

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.