early onset absence epilepsy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A childhood electroclinical syndrome characterized by the occurrence of typical absence seizures starting between the age of four and ten years. (Human Disease Ontology, DOID_0050708)
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7 genes co-occuring with the disease early onset absence epilepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1 1.82187
EFHC1 EF-hand domain (C-terminal) containing 1 1.2944
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal) 1.27214
SCN1B sodium channel, voltage gated, type I beta subunit 1.11057
ADAR adenosine deaminase, RNA-specific 1.07026
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) 0.948685
ADA adenosine deaminase 0.393746