DISEASES

Disease-gene associations mined from literature

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Human genes for autosomal dominant nonsyndromic deafness 21

Autosomal dominant nonsyndromic deafness 21 [DOID:0110551]

An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 6p24.1-p22.3.

Synonyms:  autosomal dominant nonsyndromic deafness 21,  DOID:0110551,  autosomal dominant deafness 21,  DFNA21

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.