| Disease Name | phenotype | Inheritance Mode | Chr Location | Mutation Type | Gene Name | mRNA Variant | Protein Variant | Effect | Reference |
| Hearing Impairment 39 (DFNB39, HGF) | Profound prelingual hearing impairment | Autosomal Recessive | 7q11.22?q21.12 | HGF | 482?1986_1988delTGA | 0/Schultz et al., 2009 | |||
| Hearing Impairment 39 (DFNB39, HGF) | Profound prelingual hearing impairment | Autosomal Recessive | 7q11.22?q21.12 | HGF | 482+1991_2000del | 0/Schultz et al., 2009 | |||
| Hearing Impairment 39 (DFNB39, HGF) | Profound prelingual hearing impairment | Autosomal Recessive | 7q11.22?q21.12 | Splice site | HGF | 495G>A | 0/Schultz et al., 2009 |
