autosomal recessive nonsyndromic deafness 12 (Q28024592)
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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 CDH23 gene on chromosome 10q22
- DFNB12
- autosomal recessive deafness 12
- Deafness, Autosomal Recessive type 12
- DEAFNESS, AUTOSOMAL RECESSIVE 12
- DEAFNESS, AUTOSOMAL RECESSIVE 12; DFNB12
- autosomal recessive nonsyndromic deafness type 12
Language | Label | Description | Also known as |
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English | autosomal recessive nonsyndromic deafness 12 |
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 CDH23 gene on chromosome 10q22 |
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C201586
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