DISEASES

Disease-gene associations mined from literature

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Human genes for Baller-Gerold syndrome

Baller-Gerold syndrome [DOID:0050654]

A synostosis characterized by coronal craniosynostosis, short stature, and aplasia or hypoplasia of the radial bone.

Synonyms:  Baller-Gerold syndrome,  BallerGerold syndrome,  Baller-Gerold disease,  Baller-Gerold disorder,  Baller-Gerold syndromes ...

Linkouts:  OMIM

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.