| General Information | |||
|---|---|---|---|
| Term | Parkinson's disease 3 | ID (Ontology) | DOID:0111250 (Human Disease) |
| Definition | A late onset Parkinson's disease characterized by mean age of onset of 59 years and that has_material_basis_in mutation in a locus in the 2p13 chromosome region. | ||
| Also Known As | "autosomal dominant Lewy body Parkinson disease 3" ; "autosomal dominant Parkinson disease 3" ; "PARK3" (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 | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
autosomal genetic disease |__autosomal dominant disease______ Parkinson's disease | |__late onset Parkinson's disease__| Parkinson's disease 3 |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a |
autosomal dominant disease late onset Parkinson's disease |
||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
| MIM:602404 | |||