(Q28024678)
English
autosomal dominant nonsyndromic deafness 20
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the ACTG1 gene on chromosome 17q25
- DFNA20
- DFNA26
- autosomal dominant deafness 20
- autosomal dominant nonsyndromic deafness type 20
- Deafness, Autosomal Dominant type 20
- DEAFNESS, AUTOSOMAL DOMINANT 20
- DEAFNESS, AUTOSOMAL DOMINANT 20; DFNA20
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