|
General Information
|
| Term |
autosomal dominant distal hereditary motor neuronopathy 9 |
ID (Ontology) |
DOID:0111212 (Human Disease) |
| Definition |
An autosomal domiant distal hereditary motor neuronopathy that is characterized by juvenile onset of slowly progressive distal muscle weakness and atrophy affecting both the lower and upper limbs that has_material_basis_in heterozygous mutation in the WARS gene on 14q32.2. |
| Also Known As |
"DHMN9" ; "distal hereditary motor neuronopathy type 9" ; "distal hereditary motor neuropathy type IX" (for all, see Synonyms field below) |
| 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 distal hereditary motor neuronopathy 9 | 1 | for disease ribbon | autosomal dominant distal hereditary motor neuronopathy 9 | 1 | model of | autosomal dominant distal hereditary motor neuronopathy 9 | 1 |
|
Relationships