symptomatic seizures Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A seizure that occurs in the context of a brain insult (systemic, toxic, or metabolic) and may not recur when the underlying cause has been removed or the acute phase has elapsed. (Human Phenotype Ontology, HP_0011145)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011145
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Genes

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

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
GCK glucokinase (hexokinase 4)
GLUD1 glutamate dehydrogenase 1
HADH hydroxyacyl-CoA dehydrogenase
INSR insulin receptor
POMC proopiomelanocortin
PROP1 PROP paired-like homeobox 1
SLC16A1 solute carrier family 16 (monocarboxylate transporter), member 1
TBCE tubulin folding cofactor E
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor