DISEASES

Disease-gene associations mined from literature

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Human genes for familial temporal lobe epilepsy 5

Familial temporal lobe epilepsy 5 [DOID:0060752]

A temporal lobe epilepsy that has_material_basis_in heterozygous mutation in the CPA6 gene on chromosome 8q13.

Synonyms:  familial temporal lobe epilepsy 5,  DOID:0060752,  hereditary temporal lobe epilepsy 5,  ETL5

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.