| Disease ID | Source | Name | Description |
| 606346 | OMIM | Deafness, autosomal dominant, 22 (DFNA22) | A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results 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. DFNA22 is progressive and postlingual, with onset during childhood. By the age of approximately 50 years, affected individuals invariably have profound sensorineural deafness. The disease is caused by variants affecting the gene represented in this entry. |
| 606346 | OMIM | Deafness, autosomal dominant, 22 (DFNA22) | A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results 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. DFNA22 is progressive and postlingual, with onset during childhood. By the age of approximately 50 years, affected individuals invariably have profound sensorineural deafness. The disease is caused by variants affecting the gene represented in this entry. |
| 607821 | OMIM | Deafness, autosomal recessive, 37 (DFNB37) | A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results 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. The disease is caused by variants affecting the gene represented in this entry. |