DISEASES

Disease-gene associations mined from literature

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Human genes for Bardet-Biedl syndrome 19

Bardet-Biedl syndrome 19 [DOID:0110141]

A Bardet-Biedl syndrome that has_material_basis_in homozygous mutation in the IFT27 gene on chromosome 22q12.

Synonyms:  Bardet-Biedl syndrome 19,  BardetBiedl syndrome 19,  DOID:0110141,  BBS19

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.