(Q28024640)
English
autosomal recessive nonsyndromic deafness 61
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 SLC26A5 gene on chromosome 7q22
- DFNB61
- autosomal recessive deafness 61
- DEAFNESS, AUTOSOMAL RECESSIVE 61; DFNB61
- autosomal recessive nonsyndromic deafness type 61
- DEAFNESS, AUTOSOMAL RECESSIVE 61
- Deafness, Autosomal Recessive type 61
Statements
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Identifiers
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