An inherited metabolic disease that has its basis in the disruption of methylamine metabolic process.
Comprehensive, easy-to-understand information about this condition
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sarcosinemia
MONDO:0010008
dimethylglycine dehydrogenase deficiency
MONDO:0011610
inborn disorder of peptide metabolism
MONDO:0019232
inherited glutathione metabolism disease
MONDO:0040566
disorder of polyamine metabolism
MONDO:0800159