| Name | deafness, autosomal dominant 58 |
| Description | This locus was identified to map between markers D2S2259 and D2S2114 in a Brazilian family with 12 individuals affected by bilateral post-lingual and progressive hearing loss. [provided by RefSeq, Feb 2010] |
| NCBI Gene ID | 100359395 |
| 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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DFNA58 has 1 functional associations with biological entities spanning 1 categories (disease, phenotype or trait) extracted from 1 datasets.
Click the + buttons to view associations for DFNA58 from the datasets below.
If available, associations are ranked by standardized value
| Dataset | Summary | |
|---|---|---|
| OMIM Gene-Disease Associations | phenotypes associated with DFNA58 gene from the curated OMIM Gene-Disease Associations dataset. | |
