autosomal dominant nonsyndromic deafness 69 (Q28024720)
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autosomal dominant nonsyndromic deafness that has material basis in mutation in the KITLG gene on chromosome 12q21
- DCUA
- DFNA69
- autosomal dominant deafness 69
- unilateral or asymmetric congenital deafness
- Deafness, Congenital, Unilateral or Asymmetric
- autosomal dominant nonsyndromic deafness type 69
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant nonsyndromic deafness 69 |
autosomal dominant nonsyndromic deafness that has material basis in mutation in the KITLG gene on chromosome 12q21 |
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