Disease ID | Source | Name | Description |
615540 | OMIM | Deafness, autosomal recessive, 76 (DFNB76) | A form of non-syndromic sensorineural deafness, a disorder resulting from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. DFNB76 affected individuals have onset of progressive high frequency hearing impairment between birth and 6 years of age. The hearing loss is severe at high frequencies by adulthood. The disease is caused by variants affecting the gene represented in this entry. |