DISEASES

Disease-gene associations mined from literature

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Human genes for myotonia congenita

Myotonia congenita [DOID:2106]

A muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres.

Synonyms:  myotonia congenita,  DOID:2106,  myotonia congenitas,  Congenital myotonia, autosomal dominant form,  Thomsen disease ...

Linkouts:  OMIM #1 #2 #3

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.