|
General Information
|
| Term |
Parkinson's disease 7 |
ID (Ontology) |
DOID:0060370 (Human Disease) |
| Definition |
An early-onset Parkinson's disease that has_material_basis_in homozygous or compound heterozygous mutation in the DJ1 gene on chromosome 1p36. |
| Also Known As |
"autosomal recessive early-onset Parkinson disease 7" ; "autosomal recessive early-onset Parkinson's disease 7" |
| 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)
|
| Data Class | Field | Records |
|---|
|
| Alleles (FBal) | HUMAN_DISEASE_INTERACTIONS | 12 | | Human Disease Models (FBhh) | DOID | 1 |
|
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
| Full annotation statements | Relevant FlyBase reports |
|---|
| Alleles | Genes | Human Disease Models |
|---|
Parkinson's disease 7 | 13 | 8 | 1 | ameliorates | Parkinson's disease 7 | 6 | -- | -- | for disease ribbon | Parkinson's disease 7 | -- | 2 | -- | model of | Parkinson's disease 7 | 7 | 2 | -- |
|
Relationships