|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A congenital defect of development characterized by absence of the lacrimal gland. (Human Phenotype Ontology, HP_0007656)|
|Downloads & Tools|
3 genes associated with the lacrimal gland aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.