opsoclonus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Spontaneous, non-rhythmic, multi-directional, chaotic movements of the eyes, giving the appearance of agitation. There may be bursts of conjugate movement of the eyes in varying directions and of varying amplitude. (Human Phenotype Ontology, HP_0010543)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010543
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Genes

1 genes associated with the opsoclonus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NME1 NME/NM23 nucleoside diphosphate kinase 1