(Q28024639)
English
autosomal recessive nonsyndromic deafness 6
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 TMIE gene on chromosome 3p21
- DFNB6
- autosomal recessive deafness 6
- autosomal recessive nonsyndromic deafness type 6
- DEAFNESS, AUTOSOMAL RECESSIVE 6; DFNB6
- DEAFNESS, AUTOSOMAL RECESSIVE 6
- Neurosensory Nonsyndromic Recessive Deafness 6
- Deafness, Autosomal Recessive type 6
Statements
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Identifiers
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