autosomal dominant nonsyndromic deafness 3A (Q28024692)
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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
| Language | Label | Description | Also known as |
|---|---|---|---|
| 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 |
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