DISEASES - autosomal recessive nonsyndromic deafness 39

Human genes for autosomal recessive nonsyndromic deafness 39

Autosomal recessive nonsyndromic deafness 39 [DOID:0110497]

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21.

Synonyms: autosomal recessive nonsyndromic deafness 39, DOID:0110497, autosomal recessive deafness 39, DFNB39

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.