DISEASES

Disease-gene associations mined from literature

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Human genes for familial febrile seizures 11

Familial febrile seizures 11 [DOID:0111308]

A familial febrile seizures that has_material_basis_in homozygous mutation in CPA6 on chromosome 8p13.2.

Synonyms:  familial febrile seizures 11,  DOID:0111308,  hereditary febrile seizures 11,  familial febrile convulsions 11,  FEB11 ...

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.