DISEASES - autosomal dominant nonsyndromic deafness 33

Human genes for autosomal dominant nonsyndromic deafness 33

Autosomal dominant nonsyndromic deafness 33 [DOID:0110562]

An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 13q34.

Synonyms: autosomal dominant nonsyndromic deafness 33, DOID:0110562, autosomal dominant deafness 33, DFNA33

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.