|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A type of cataract that is not apparent at birth but that arises in childhood or adolescence. (Human Phenotype Ontology, HP_0001118)|
|Downloads & Tools|
2 genes associated with the juvenile cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.