autosomal recessive nonsyndromic deafness 22 (Q28024605)
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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 OTOA gene on chromosome 16p12
- DFNB22
- autosomal recessive deafness 22
- autosomal recessive nonsyndromic deafness type 22
- Deafness, Autosomal Recessive type 22
- DEAFNESS, AUTOSOMAL RECESSIVE 22; DFNB22
- DEAFNESS, AUTOSOMAL RECESSIVE 22
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive nonsyndromic deafness 22 |
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 OTOA gene on chromosome 16p12 |
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