DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for autosomal recessive nonsyndromic deafness 6

Autosomal recessive nonsyndromic deafness 6 [DOID:0110512]

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the TMIE gene on chromosome 3p21.

Synonyms:  autosomal recessive nonsyndromic deafness 6,  DOID:0110512,  autosomal recessive deafness 6,  DFNB6

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.