epilepsia partialis continua Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A form of partial status epilepticus with simple motor manifestations that are maintained for over one hour, with clonic activity restricted to one body part and recurring at fairly regular intervals. (Human Phenotype Ontology, HP_0012847)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012847
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Genes

2 genes associated with the epilepsia partialis continua phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C10ORF2 chromosome 10 open reading frame 2
POLG polymerase (DNA directed), gamma