(Q28024662)
English
autosomal recessive nonsyndromic deafness 9
autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually severe to profound, stable hearing loss and has material basis in mutation in the OTOF gene on chromosome 2p23
- DFNB9
- NRSD9
- autosomal recessive deafness 9
- neurosensory nonsyndromic recessive deafness 9
- Auditory Neuropathy, Nonsyndromic Recessive
- Auditory Neuropathy, Autosomal Recessive, 1
- autosomal recessive nonsyndromic deafness type 9
- Deafness, Autosomal Recessive type 9
- DEAFNESS, AUTOSOMAL RECESSIVE 9; DFNB9
- DEAFNESS, AUTOSOMAL RECESSIVE 9
Statements
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Identifiers
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