|Dataset||DISEASES Text-mining Gene-Disease Assocation Evidence Scores|
|Category||disease or phenotype associations|
|Description||A mitochondrial metabolism disease that has_material_basis_in a mutation in the SCO2 gene which encodes a COX assembly factor and results in deficiency of cytochrome c oxidase. (Human Disease Ontology, DOID_0050713)|
|Downloads & Tools|
1 genes co-occuring with the disease fatal infantile encephalocardiomyopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
|ACAD9||acyl-CoA dehydrogenase family, member 9||2.53309|