|
General Information
|
| Term |
autosomal dominant nonsyndromic deafness 84 |
ID (Ontology) |
DOID:0070604 (Human Disease) |
| Definition |
An autosomal dominant nonsyndromic deafness characterized by bilateral, progressive sensorineural hearing loss with variable onset and audiogram shape that has_material_basis_in heterozygous mutation in the ATP11A gene on chromosome 13q34. |
| Also Known As |
"autosomal dominant deafness 84" ; "DFNA84" |
| Comment |
|
|
Links to External Ontologies
|
|
DO.org
|
|
Annotations
|
|
Records annotated with this term OR any of its CHILD TERMS
|
|
|
|
Records annotated with this exact term (annotations to child terms are NOT included)
|
|
No relevant records available
|
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
| Full annotation statements | Relevant FlyBase reports |
|---|
| Genes |
|---|
autosomal dominant nonsyndromic deafness 84 | 2 | for disease ribbon | autosomal dominant nonsyndromic deafness 84 | 2 | model of | autosomal dominant nonsyndromic deafness 84 | 2 |
|