DISEASES - autosomal recessive nonsyndromic deafness 83

Human genes for autosomal recessive nonsyndromic deafness 83

Autosomal recessive nonsyndromic deafness 83 [DOID:0110528]

An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 9p23-p21.2.

Synonyms: autosomal recessive nonsyndromic deafness 83, DOID:0110528, autosomal recessive deafness 83, DFNB83

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.