|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A ptosis characterized by eyelid drop present at birth. (Human Disease Ontology, DOID_0060261)|
|Downloads & Tools|
1 genes associated with the congenital ptosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|ZFHX4||zinc finger homeobox 4|