Dimethylglycine Dehydrogenase Deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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://ctdbase.org/detail.go?type=disease&acc=MESH:C565278
Similar Terms
Downloads & Tools


1 genes/proteins associated with the disease Dimethylglycine Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
DMGDH dimethylglycine dehydrogenase 2.88009