(Q28024592)
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
- 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
Statements
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C201586
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Identifiers
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