(Q28024687)
English
autosomal dominant nonsyndromic deafness 2B
An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the fourth decade of life with by high frequency progressive hearing loss and has material basis in mutation in the GJB3 gene on chromosome 1p34.3.
- DFNA2B
- autosomal dominant deafness 2B
- autosomal dominant nonsyndromic deafness type 2B
- Deafness, Autosomal Dominant type 2B
- DEAFNESS, AUTOSOMAL DOMINANT 2B
- DEAFNESS, AUTOSOMAL DOMINANT 2B; DFNA2B
Statements
1 reference
1 reference
Identifiers
1 reference
1 reference
2 references
1 reference
1 reference