|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A type of congenital cataract in which the opacities are confined to a small central area within the embryonic or fetal nuclei of the Iens. The remaining lens is clear. (Human Phenotype Ontology, HP_0008024)|
|Downloads & Tools|
3 genes associated with the congenital nuclear cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.