DISEASES

Disease-gene associations mined from literature

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Human genes for fetal valproate syndrome

Fetal valproate syndrome [DOID:0060471]

A syndrome characterized by distinctive facial appearance, a cluster of minor and major anomalies and central nervous system dysfunction.

Synonyms:  fetal valproate syndrome,  DOID:0060471,  fetal valproate disease,  fetal valproate disorder,  fetal valproate 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.