autosomal recessive nonsyndromic deafness 23 (Q28024606)
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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 PCDH15 gene on chromosome 10q21
- DFNB23
- autosomal recessive deafness 23
- DEAFNESS, AUTOSOMAL RECESSIVE 23
- DEAFNESS, AUTOSOMAL RECESSIVE 23; DFNB23
- autosomal recessive nonsyndromic deafness type 23
- Deafness, Autosomal Recessive type 23
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive nonsyndromic deafness 23 |
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 PCDH15 gene on chromosome 10q21 |
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