|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|
|Expression in Tissues and Cell Lines||
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
|OMIM Gene-Disease Associations||phenotypes associated with DFNA58 gene from the curated OMIM Gene-Disease Associations dataset.|