|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Absence of molybdenum cofactor(2-), a cofactor for enzymes including sulfite oxidase, xanthine oxidoreductase, and aldehyde oxidase. (Human Phenotype Ontology, HP_0003570)|
|Downloads & Tools|
2 genes associated with the molybdenum cofactor deficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.