| Disease Name | phenotype | Inheritance Mode | Chr Location | Mutation Type | Gene Name | mRNA Variant | Protein Variant | Effect | Reference |
| Hearing Impairment 24 (DFNB24, RDX) | Neurosensory hearing loss | Autosomal Recessive | 11q22.3 | Missense | RDX | 1732G>A | Asp578Asn | Amino Acid Substitution | 0/Khan et al., 2007 |
| Hearing Impairment 24 (DFNB24, RDX) | Sensorineural hearing loss | Autosomal Recessive | 11q22.3 | Insertion | RDX | 1404_1405insG | Ala469fs*487 | Frame shift mutation & PTC | 0/Khan et al., 2007 |
| Hearing Impairment 24 (DFNB24, RDX) | Sensorineural hearing loss | Autosomal Recessive | 11q22.3 | Nonsense | RDX | 463C>T | Gln155* | Premature Termination | 0/Khan et al., 2007 |
| Hearing Impairment 24 (DFNB24, RDX) | Hearing loss | Autosomal Recessive | 11q22.3 | Deletion | RDX | 1076_1079delTTAA | Ile359Lysfs*6 | Frame shift mutation & PTC | 0/Lee et al., 2011 |
