|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||An organic acidemia that involves an accumulation of methylmalonic acid in the blood. (Human Disease Ontology, DOID_14749)|
|Downloads & Tools|
1 genes/proteins associated with the disease Methylmalonic Aciduria due to Methylmalonyl-CoA Mutase Deficiency from the curated CTD Gene-Disease Associations dataset.
|MUT||methylmalonyl CoA mutase||2.88009|