autosomal dominant nonsyndromic deafness 1 (Q28024668)
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autosomal dominant nonsyndromic deafness that is characterized by low frequency progressive hearing loss and has material basis in mutation in the DIAPH1 gene on chromosome 5q31
- DFNA1
- Konigsmark syndrome
- LFHL1
- autosomal dominant deafness 1
- hereditary low frequency hearing loss 1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant nonsyndromic deafness 1 |
autosomal dominant nonsyndromic deafness that is characterized by low frequency progressive hearing loss and has material basis in mutation in the DIAPH1 gene on chromosome 5q31 |
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1 reference