oculomotor nerve palsy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012246
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1 genes associated with the oculomotor nerve palsy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
TRPV4 transient receptor potential cation channel, subfamily V, member 4