(Q28024642)
English
autosomal recessive nonsyndromic deafness 63
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 LRTOMT gene on chromosome 11q13
- DFNB63
- autosomal recessive deafness 63
- DEAFNESS, AUTOSOMAL RECESSIVE 63; DFNB63
- Deafness, Autosomal Recessive type 63
- autosomal recessive nonsyndromic deafness type 63
- DEAFNESS, AUTOSOMAL RECESSIVE 63
Statements
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Identifiers
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