bilateral convulsive seizures Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Bilateral convulsive seizures are focal seizure with secondary bilateral motor phenomena, not primary generalized seizures. (Human Phenotype Ontology, HP_0007334)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007334
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Genes

4 genes associated with the bilateral convulsive seizures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
LGI1 leucine-rich, glioma inactivated 1
NHLRC1 NHL repeat containing E3 ubiquitin protein ligase 1
SCN2A sodium channel, voltage gated, type II alpha subunit