congenital nystagmus Gene Set

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

Symbol Name
CNGB3 cyclic nucleotide gated channel beta 3
FRMD7 FERM domain containing 7
LRP5 low density lipoprotein receptor-related protein 5
PAX6 paired box 6