DISEASES

Disease-gene associations mined from literature

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Human genes for familial temporal lobe epilepsy 3

Familial temporal lobe epilepsy 3 [DOID:0060750]

A temporal lobe epilepsy characterized by simple or complex partial seizures often accompanied by intense feelings of deja or altered awareness and that has_material_basis_in variation in the chromosome region 4q13.2-q21.3.

Synonyms:  familial temporal lobe epilepsy 3,  DOID:0060750,  hereditary temporal lobe epilepsy 3,  familial mesial temporal lobe epilepsy,  FMTLE ...

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.