|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Lack of transparency of the corneal epithelium. (Human Phenotype Ontology, HP_0007727)|
|Downloads & Tools|
1 genes associated with the opacification of the corneal epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|ALDH3A2||aldehyde dehydrogenase 3 family, member A2|