| General Information | |||
|---|---|---|---|
| Term | Alzheimer's disease 9 | ID (Ontology) | DOID:0111364 (Human Disease) |
| Definition | An Alzheimer's disease that has_material_basis_in heterozygous mutation in the ABCA7 gene on chromosome 19p13.3. | ||
| Also Known As | "AD9" ; "Alzheimer's disease 9, late onset" | ||
| 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
|
|||
|
||||||
autosomal genetic disease |__autosomal dominant disease__ tauopathy | |__Alzheimer's disease_________| Alzheimer's disease 9 1 rec. |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a |
autosomal dominant disease Alzheimer's disease |
||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
| MIM:608907 | |||