|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A sectoral indentation of the crystalline lens, usually due to zonular weakness or absence. (Human Phenotype Ontology, HP_0100719)|
|Downloads & Tools|
3 genes associated with the lens coloboma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.