| Disease Name | phenotype | Inheritance Mode | Chr Location | Mutation Type | Gene Name | mRNA Variant | Protein Variant | Effect | Reference |
| Hearing Impairment 96 (DFNB96) | severe to profound hearing loss | Autosomal Recessive | 1p36.31-p36.13 | 0/Ansar et al., 2011 | |||||
| Hearing Impairment 89 (DFNB89) | moderate-to severe hearing loss | Autosomal Recessive | 16q21-q23.2 | 0/Basit et al., 2011 |
