DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for autosomal dominant nonsyndromic deafness 67

Autosomal dominant nonsyndromic deafness 67 [DOID:0110588]

An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the OSBPL2 gene on chromosome 20q13.

Synonyms:  autosomal dominant nonsyndromic deafness 67,  DOID:0110588,  autosomal dominant deafness 67,  DFNA67

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.