| Disease ID | Source | Name | Description |
| 603720 | OMIM | Deafness, autosomal recessive, 16 (DFNB16) | 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. |
| 611102 | OMIM | Deafness-infertility syndrome (DIS) | Characterized by deafness and infertility and is caused by large contiguous gene deletions at 15q15.3 that removes both STRC and CATSPER2 genes. The disease is caused by variants affecting the gene represented in this entry. |