|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Absence or underdevelopment of the eyelid. (Human Phenotype Ontology, HP_0011226)|
|Downloads & Tools|
1 genes associated with the aplasia/hypoplasia affecting the eyelid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.