autosomal recessive nonsyndromic deafness 29 (Q28024614)
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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 CLDN14 gene on chromosome 21q22
- DFNB29
- autosomal recessive deafness 29
- autosomal recessive nonsyndromic deafness type 29
- DEAFNESS, AUTOSOMAL RECESSIVE 29; DFNB29
- Deafness, Autosomal Recessive type 29
- DEAFNESS, AUTOSOMAL RECESSIVE 29
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal recessive nonsyndromic deafness 29 |
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 CLDN14 gene on chromosome 21q22 |
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