nonsyndromic recessive deafness

Genetics

• autosomal recessive
• associated with defects in
  • harmonin gene
  • otoferlin gene
  • COMT2 gene
  • SLC26A5 gene

Laboratory

• SLC26A5 gene mutation

More general terms

• familial deafness

Database

• OMIM: https://mirror.omim.org/entry/601071