(Q28024596)
English
autosomal recessive nonsyndromic deafness 16
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 STRC gene on chromosome 15q15
- DFNB16
- autosomal recessive deafness 16
- DEAFNESS, AUTOSOMAL RECESSIVE 16
- DEAFNESS, AUTOSOMAL RECESSIVE 16; DFNB16
- autosomal recessive nonsyndromic deafness type 16
- Deafness, Autosomal Recessive type 16
Statements
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Identifiers
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