autosomal dominant nonsyndromic deafness 20 (Q28024678)
Jump to navigation
Jump to search
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the ACTG1 gene on chromosome 17q25
- DFNA20
- DFNA26
- autosomal dominant deafness 20
- autosomal dominant nonsyndromic deafness type 20
- Deafness, Autosomal Dominant type 20
- DEAFNESS, AUTOSOMAL DOMINANT 20
- DEAFNESS, AUTOSOMAL DOMINANT 20; DFNA20
Language | Label | Description | Also known as |
---|---|---|---|
English | autosomal dominant nonsyndromic deafness 20 |
autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has material basis in mutation in the ACTG1 gene on chromosome 17q25 |
|
Statements
1 reference
Identifiers
1 reference
1 reference
2 references
1 reference
1 reference
1 reference