|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A congenital defect resulting in absence of the lacrimal duct. (Human Phenotype Ontology, HP_0007925)|
|Downloads & Tools|
4 genes associated with the lacrimal duct aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.