DISEASES

Disease-gene associations mined from literature

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Human genes for infancy electroclinical syndrome

Infancy electroclinical syndrome [DOID:0050703]

An electroclinical syndrome with onset in infancy occurring between birth and one year of age.

Synonyms:  infancy electroclinical syndrome,  DOID:0050703,  infancy electroclinical disease,  infancy electroclinical disorder,  infancy electroclinical syndromes

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.