|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Cerulean cataracts are a kind of congenital cataract having peripheral bluish and white opacifications in concentric layers with occasional central lesions arranged radially. Although the opacities may be observed during fetal development and childhood, usually visual acuity is only mildly reduced until adulthood, when lens extraction is generally necessary. (Human Phenotype Ontology, HP_0007976)|
|Downloads & Tools|
2 genes associated with the cerulean cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.