| Disease Name | phenotype | Inheritance Mode | Chr Location | Mutation Type | Gene Name | mRNA Variant | Protein Variant | Effect | Reference |
| Hearing Impairment 37 (DFNB37, MYO6) | Severe-to-profound hearing loss | Autosomal Recessive | 6q13 | Insertion | MYO6 | 36-37insT | Frame shift mutation & PTC | 0/Ahmed et al., 2003 | |
| Hearing Impairment 37 (DFNB37, MYO6) | severe to profound hearing loss | Autosomal Recessive | 6q13 | Nonsense | MYO6 | 3496C>T | Arg1166* | Premature Termination | 0/Ahmed et al., 2003 |
| Hearing Impairment 37 (DFNB37, MYO6) | severe to profound hearing loss | Autosomal Recessive | 6q13 | Missense | MYO6 | 647A>T | Glu216Val | Amino Acid Substitution | 0/Ahmed et al., 2003 |
