(Q28024676)
English
autosomal dominant nonsyndromic deafness 17
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the MYH9 gene on chromosome 22q12
- DFNA17
- autosomal dominant deafness 17
- DEAFNESS, AUTOSOMAL DOMINANT 17
- autosomal dominant nonsyndromic deafness type 17
- DEAFNESS, AUTOSOMAL DOMINANT 17; DFNA17
- Cochleosaccular Degeneration
- Deafness, Autosomal Dominant type 17
Statements
1 reference
1 reference
Identifiers
1 reference
2 references
1 reference
1 reference
1 reference