|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A congenital cataract in which opacity is limited to layers of the lens external to the nucleus (i.e., the perinuclear region), i.e., between the nuclear and cortical layers of the lens. (Human Phenotype Ontology, HP_0007971)|
|Downloads & Tools|
2 genes associated with the lamellar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.