DISEASES

Disease-gene associations mined from literature

JensenLab
SearchDownloadsAbout

Human genes for alternating hemiplegia of childhood

Alternating hemiplegia of childhood [DOID:0050635]

A hemiplegia characterized by recurrent episodes of temporary weakness or complete paralysis on one or both sides of the body.

Synonyms:  alternating hemiplegia of childhood,  DOID:0050635,  alternating hemiplegia of childhoods,  AHC

Linkouts:  OMIM #1 #2

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.

Currently maintained by Qingyao Huang at Swiss Institute of Bioinformatics, University of Zurich. Licensed under CC BY 4.0.