|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A kind of congenital cataract that is characterized by a hollow sphere of punctate opacities involving the fetal nucleus and that usually occurs bilaterally. (Human Phenotype Ontology, HP_0010693)|
|Downloads & Tools|
5 genes associated with the pulverulent cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.