| 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 |
| API | |
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| Predicted Functions |
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| Co-expressed Genes |
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| Expression in Tissues and Cell Lines |
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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
| Dataset | Summary | |
|---|---|---|
| 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. | |
