DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for Bartter disease type 4a

Bartter disease type 4a [DOID:0110145]

A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the BSND gene on chromosome 1p32.

Synonyms:  Bartter disease type 4a,  DOID:0110145,  BARTS4A,  Bartter syndrome type 4a,  neonatal Bartter syndrome with sensorineural deafness ...

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.