DISEASES

Disease-gene associations mined from literature

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Human genes for Bardet-Biedl syndrome 17

Bardet-Biedl syndrome 17 [DOID:0110139]

A Bardet-Biedl syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the LZTFL1 gene on chromosome 3p21.

Synonyms:  Bardet-Biedl syndrome 17,  BardetBiedl syndrome 17,  DOID:0110139,  BBS17

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.