DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for Fanconi anemia complementation group O

Fanconi anemia complementation group O [DOID:0111096]

A Fanconi anemia that has_material_basis_in homozygous mutation in the RAD51C gene on chromosome 17q21-q24.

Synonyms:  Fanconi anemia complementation group O,  DOID:0111096,  Fanconi anemia complementation group Os,  FANCO,  FANCOs

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.