|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes/proteins associated with the disease Dimethylglycine Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.