(Q28024636)
English
autosomal recessive nonsyndromic deafness 53
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 COL11A2 gene on chromosome 6p21
- DFNB53
- autosomal recessive deafness 53
- Deafness, Autosomal Recessive type 53
- DEAFNESS, AUTOSOMAL RECESSIVE 53
- DEAFNESS, AUTOSOMAL RECESSIVE 53; DFNB53
- autosomal recessive nonsyndromic deafness type 53
Statements
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Identifiers
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