DFNB37 is caused by homozygous mutation in the gene encoding myosin VI on chromosome 6q14.
Diseases of the ear and mastoid process
Other disorders of ear
Autosomal recessive
6q14.1
DFNB37 is caused by homozygous mutation in the gene encoding myosin VI on chromosome 6q14.
| Subject ID | Country | Sex | Family History | Parental Consanguinity | HPO Terms | Variant | Zygosity | Mode of Inheritance | Reference | Remarks |
|---|---|---|---|---|---|---|---|---|---|---|
| 607821.G | United Arab Emirates | Unknown | Congenital sensorineural hearing impairm... Congenital sensorineural hearing impairment  | NM_004999.4:c.2751dup | Homozygous | Autosomal, Recessive | Elsayed O and Al-Shamsi A. 2022 | Two patients. No oth... |