DISEASES

Disease-gene associations mined from literature

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Human genes for Unverricht-Lundborg syndrome

Unverricht-Lundborg syndrome [DOID:3535]

A progressive myoclonus epilepsy characterized by onset between 6 and 13 years of age of action- and stimulus-sensitive myoclonus, tonic-clonic seizures with ataxia, and a mild cognitive decline.

Synonyms:  Unverricht-Lundborg syndrome,  DOID:3535,  UnverrichtLundborg syndrome,  Unverricht-Lundborg disease,  Unverricht-Lundborg disorder ...

Linkouts:  OMIM

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.