DISEASES - autosomal recessive nonsyndromic deafness 55

Human genes for autosomal recessive nonsyndromic deafness 55

Autosomal recessive nonsyndromic deafness 55 [DOID:0110510]

An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 4q12-q13.2.

Synonyms: autosomal recessive nonsyndromic deafness 55, DOID:0110510, autosomal recessive deafness 55, DFNB55

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.