Dimethylglycine dehydrogenase deficiency Gene Set

Dataset ClinVar Gene-Phenotype 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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Genes

1 genes associated with the Dimethylglycine dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
DMGDH dimethylglycine dehydrogenase