dimethylglycine dehydrogenase deficiency Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Dimethylglycine dehydrogenase deficiency is 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. (Orphanet Rare Disease Ontology, Orphanet_243343)
External Link http://www.omim.org/entry/605850
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1 genes associated with the dimethylglycine dehydrogenase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
DMGDH dimethylglycine dehydrogenase