| General Information | |||
|---|---|---|---|
| Term | amyotrophic lateral sclerosis type 13 | ID (Ontology) | DOID:0060204 (Human Disease) |
| Definition | An amyotrophic lateral sclerosis where a mutation that has_material_basis_in the ATXN2 gene on chromosome 12 contributes to suscepitbility. | ||
| Also Known As | "ALS13" ; "amyotrophic lateral sclerosis 13" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
motor neuron disease |__amyotrophic lateral sclerosis |__amyotrophic lateral sclerosis type 13 |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | amyotrophic lateral sclerosis | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||