autosomal recessive nonsyndromic deafness 3 (Q28024615)

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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 MYO15A gene on chromosome 17p11
  • DFNB3
  • NRSD3
  • autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3
  • Deafness, Autosomal Recessive type 3
  • DEAFNESS, AUTOSOMAL RECESSIVE 3; DFNB3
  • DEAFNESS, AUTOSOMAL RECESSIVE 3
  • Neurosensory Nonsyndromic Recessive Deafness 3
  • autosomal recessive nonsyndromic deafness type 3
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English
autosomal recessive nonsyndromic deafness 3
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 MYO15A gene on chromosome 17p11
  • DFNB3
  • NRSD3
  • autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3
  • Deafness, Autosomal Recessive type 3
  • DEAFNESS, AUTOSOMAL RECESSIVE 3; DFNB3
  • DEAFNESS, AUTOSOMAL RECESSIVE 3
  • Neurosensory Nonsyndromic Recessive Deafness 3
  • autosomal recessive nonsyndromic deafness type 3

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