(Q28024681)
English
autosomal dominant nonsyndromic deafness 23
autosomal dominant nonsyndromic deafness that is characterized by prelingual onset with high frequency progressive hearing loss and has material basis in mutation in the SIX1 gene on chromosome 14q23
- DFNA23
- autosomal dominant deafness 23
- Deafness, Autosomal Dominant type 23
- DEAFNESS, AUTOSOMAL DOMINANT 23
- autosomal dominant nonsyndromic deafness type 23
- DEAFNESS, AUTOSOMAL DOMINANT 23; DFNA23
Statements
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Identifiers
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