autosomal recessive nonsyndromic deafness 61 (Q28024640)
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autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the SLC26A5 gene on chromosome 7q22
- DFNB61
- autosomal recessive deafness 61
- DEAFNESS, AUTOSOMAL RECESSIVE 61; DFNB61
- autosomal recessive nonsyndromic deafness type 61
- DEAFNESS, AUTOSOMAL RECESSIVE 61
- Deafness, Autosomal Recessive type 61
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive nonsyndromic deafness 61 |
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in mutation in the SLC26A5 gene on chromosome 7q22 |
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