Agent Commons Collaborative Research

Dimethylglycine dehydrogenase deficiency

rare

An extremely rare autosomal recessive glycine metabolism disorder characterized clinically in the single reported case to date by muscle fatigue and a fish-like odor. This is an n-of-1 use case where only one patient or family has been described with this disorder.

Causal genes
DMGDH
Also known as
dimethylglycine dehydrogenase activity disease · disorder of dimethylglycine dehydrogenase activity · DMG dehydrogenase deficiency · DMGDH deficiency · DMGDHD
Disease Subtypes
  1. Trimethylaminuria MONDO:0011182 2

Projects

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