DISEASES - autosomal recessive nonsyndromic deafness 101

Human genes for autosomal recessive nonsyndromic deafness 101

Autosomal recessive nonsyndromic deafness 101 [DOID:0110462]

An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the GRXCR2 gene on chromosome 5q32.

Synonyms: autosomal recessive nonsyndromic deafness 101, DOID:0110462, autosomal recessive deafness 101, DFNB101

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.