|Dataset||DISEASES Text-mining Gene-Disease Assocation Evidence Scores|
|Category||disease or phenotype associations|
|Description||A mitochondrial metabolism disease that is characterized by a deficiency of CoQ10 resulting from reduced biosynthesis. (Human Disease Ontology, DOID_0050730)|
|Downloads & Tools|
1 genes co-occuring with the disease coenzyme q10 deficiency disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
|ENO3||enolase 3 (beta, muscle)||1.9136|