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| References | OMIM | Gene | GeneReviews | HGMD | HGNC |
| GENATLAS PHENOTYPE |
| last update : 18 |
| Symbol | DFNA23 |
| Location | 14q21-q22 |
| HGNC id | 2795 |
| Name | neurosensory deafness 23 |
| Corresponding gene | SIX1 |
| Main clinical features | non syndromic, prelingual, stable, with hearing ability ranging from normal hearing to mild hearing loss in low frequencies, normal hearing to profound hearing loss in mid-frequencies, and moderate to profound hearing loss in high frequencies |
| Genetic determination | autosomal dominant |
| Function/system disorder | ear |
| Type | disease |
| Remark(s) |