(Q28024672)
English
autosomal dominant nonsyndromic deafness 13
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has material basis in mutation in the COL11A2 gene on chromosome 6p21
- DFNA13
- autosomal dominant deafness 13
- autosomal dominant nonsyndromic deafness type 13
- DEAFNESS, AUTOSOMAL DOMINANT 13; DFNA13
- DEAFNESS, AUTOSOMAL DOMINANT 13
- Deafness, Autosomal Dominant type 13
Statements
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Identifiers
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