|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Reduced ability to control the movement of the eye associated with damage to the third cranial nerve (the oculomotor nerve). (Human Phenotype Ontology, HP_0012246)|
|Downloads & Tools|
1 genes associated with the oculomotor nerve palsy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|TRPV4||transient receptor potential cation channel, subfamily V, member 4|