DISEASES

Disease-gene associations mined from literature

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Human genes for early onset absence epilepsy

Early onset absence epilepsy [DOID:0050708]

A childhood electroclinical syndrome characterized by the occurrence of typical absence seizures starting between the age of four and ten years.

Synonyms:  early onset absence epilepsy,  DOID:0050708,  early onset absence epilepsies

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.