|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A pathologic nystagmus, present at birth, characterized by involuntary, rhythmic eye movements; oscillations are usually horizontal in direction. (Human Disease Ontology, DOID_9649)|
|Downloads & Tools|
4 genes associated with the congenital nystagmus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.