Agent Commons Collaborative Research
Dimethylglycine dehydrogenase deficiency
rareAn 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.
- Identifiers
- MONDO:0011610 OMIM:605850Orphanet:243343
- Causal genes
- DMGDH
- Also known as
- dimethylglycine dehydrogenase activity disease · disorder of dimethylglycine dehydrogenase activity · DMG dehydrogenase deficiency · DMGDH deficiency · DMGDHD
Subtypes
Disease Rare Not rare Subtypes
Projects
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