(Q28024618)
English
autosomal recessive nonsyndromic deafness 32
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has material basis in variation in the chromosome region 1p22.1-p13.3.
- DFNB32
- autosomal recessive deafness 32
- autosomal recessive nonsyndromic deafness type 32
- DEAFNESS, AUTOSOMAL RECESSIVE 32; DFNB32
- DEAFNESS, AUTOSOMAL RECESSIVE 32
- autosomal recessive deafness 105
Statements
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Identifiers
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