autosomal dominant nonsyndromic sensorineural deafness 23

Pathology

• sensorineural deafness
• a conductive hearing loss component present in some but not all patients

Genetics

• autosomal dominant
• associated with defects in SIX1

Clinical manifestations

• prelingual, bilateral, symmetric hearing loss

More general terms

• familial deafness

Database

• OMIM: https://mirror.omim.org/entry/605192