DISEASES

Disease-gene associations mined from literature

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Human genes for calcium oxalate nephrolithiasis

Calcium oxalate nephrolithiasis [DOID:0080652]

A nephrolithiasis that is characterized by characterized by stones composed of calcium oxalate and that has_material_basis_in compound heterozygous mutation in the SLC26A1 gene on chromosome 4p16.

Synonyms:  calcium oxalate nephrolithiasis,  calcium oxalate nephrolithiasises,  DOID:0080652

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.