DISEASES

Disease-gene associations mined from literature

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Human genes for progressive myoclonus epilepsy

Progressive myoclonus epilepsy [DOID:891]

A variable age at onset electroclinical syndrome characterised by a relentlessly progressive disease course until death.

Synonyms:  progressive myoclonus epilepsy,  DOID:891,  progressive myoclonus epilepsies,  PME,  progressive myoclonic epilepsy ...

Linkouts:  OMIM #1 #2 #3 #4 #5 #6

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.