extratemporal epilepsy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An epilepsy syndrome that is located_in an area of the brain other than the temporal lobe. (Human Disease Ontology, DOID_2544)
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10 genes co-occuring with the disease extratemporal epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
KHDRBS3 KH domain containing, RNA binding, signal transduction associated 3 1.81058
HIF3A hypoxia inducible factor 3, alpha subunit 1.30576
CLIP1 CAP-GLY domain containing linker protein 1 1.26647
MYRF myelin regulatory factor 1.25428
EXT1 exostosin glycosyltransferase 1 1.12487
WNT10A wingless-type MMTV integration site family, member 10A 1.11435
PLP1 proteolipid protein 1 0.886799
HAS1 hyaluronan synthase 1 0.879833
SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1 0.630813
HLA-C major histocompatibility complex, class I, C 0.284728