autosomal dominant nonsyndromic deafness 2A (Q28024686)
Jump to navigation
Jump to search
An autosomal dominant nonsyndromic deafness that is characterized by high frequency progressive hearing loss and has material basis in mutation in the KCNQ4 gene on chromosome 1p34.2.
- DFNA2A
- autosomal dominant deafness 2A
- DEAFNESS, AUTOSOMAL DOMINANT 2A
- Deafness, Autosomal Dominant type 2A
- DEAFNESS, AUTOSOMAL DOMINANT 2A; DFNA2A
- autosomal dominant nonsyndromic deafness type 2A
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | autosomal dominant nonsyndromic deafness 2A |
An autosomal dominant nonsyndromic deafness that is characterized by high frequency progressive hearing loss and has material basis in mutation in the KCNQ4 gene on chromosome 1p34.2. |
|
Statements
1 reference
1 reference
3 references
Identifiers
1 reference
1 reference
2 references
1 reference
1 reference