autosomal dominant nonsyndromic sensorineural deafness 9

Genetics

• autosomal dominant
• associated with mutations in gene for cochlin

More general terms

• non-syndromic sensorineural hearing loss
• familial deafness

Database

• OMIM: https://mirror.omim.org/entry/603196
• OMIM: https://mirror.omim.org/entry/601369