(Q28024686)

English

autosomal dominant nonsyndromic deafness 2A

An autosomal dominant nonsyndromic deafness that is characterized by high frequency progressive hearing loss and has material basis in mutation in the KCNQ4 gene on chromosome 1p34.2.

  • DFNA2A
  • autosomal dominant deafness 2A
  • DEAFNESS, AUTOSOMAL DOMINANT 2A
  • Deafness, Autosomal Dominant type 2A
  • DEAFNESS, AUTOSOMAL DOMINANT 2A; DFNA2A
  • autosomal dominant nonsyndromic deafness type 2A

Statements

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit