Disease ID | Source | Name | Description |
614899 | OMIM | Deafness, autosomal recessive, 93 (DFNB93) | A form of non-syndromic deafness characterized by stable, bilateral, symmetric, prelingual moderate to severe deafness. Hearing impairment is slightly more pronounced in the mid-frequencies, resulting in a distinctive shallow U-shaped audiogram. The disease is caused by variants affecting the gene represented in this entry. |