autosomal recessive nonsyndromic deafness 59 (Q28024638)
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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 DFNB59 gene on chromosome 2q31
- DFNB59
- autosomal recessive deafness 59
- autosomal recessive nonsyndromic deafness type 59
- Deafness, Autosomal Recessive type 59
- DEAFNESS, AUTOSOMAL RECESSIVE 59
- DEAFNESS, AUTOSOMAL RECESSIVE 59; DFNB59
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive nonsyndromic deafness 59 |
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 DFNB59 gene on chromosome 2q31 |
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