DISEASES - autosomal recessive nonsyndromic deafness 51

Human genes for autosomal recessive nonsyndromic deafness 51

Autosomal recessive nonsyndromic deafness 51 [DOID:0110508]

An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 11p13-p12.

Synonyms: autosomal recessive nonsyndromic deafness 51, DOID:0110508, autosomal recessive deafness 51, DFNB51

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.