(Q28024692)
English
autosomal dominant nonsyndromic deafness 3A
autosomal dominant nonsyndromic deafness that is characterized by prelingual, high frequency hearing loss and has material basis in mutation in the GJB2 gene on chromosome 13q12
- DFNA3A
- autosomal dominant deafness 3A
- autosomal dominant nonsyndromic deafness type 3A
- DEAFNESS, AUTOSOMAL DOMINANT 3A
- Deafness, Autosomal Dominant type 3A
- DEAFNESS, AUTOSOMAL DOMINANT 3A; DFNA3A
Statements
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Identifiers
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