|Name||deafness, autosomal recessive 83|
|Description||This locus, identified by homozygosity mapping, overlaps that of DFNA47. It may be that mutations of the same gene are responsible for recessive and dominant hearing loss. [provided by RefSeq, Feb 2010]|
|NCBI Gene ID||100359400|
|Expression in Tissues and Cell Lines||
DFNB83 has 2 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 2 datasets.
Click the + buttons to view associations for DFNB83 from the datasets below.
If available, associations are ranked by standardized value
|CTD Gene-Disease Associations||diseases associated with DFNB83 gene/protein from the curated CTD Gene-Disease Associations dataset.|
|OMIM Gene-Disease Associations||phenotypes associated with DFNB83 gene from the curated OMIM Gene-Disease Associations dataset.|