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General Information
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| Term |
Parkinson's disease 6 |
ID (Ontology) |
DOID:0060369 (Human Disease) |
| Definition |
An early-onset Parkinson's disease that has_material_basis_in mutations in the PINK1 gene on chromosome 1p36.12. |
| Also Known As |
"autosomal recessive early-onset Parkinson disease 6" ; "autosomal recessive early-onset Parkinson's disease 6" ; "early-onset Parkinson disease 6" (for all, see Synonyms field below) |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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| Data Class | Field | Records |
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| Alleles (FBal) | HUMAN_DISEASE_INTERACTIONS | 121 | | Human Disease Models (FBhh) | DOID | 1 |
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Alleles | Genes | Human Disease Models |
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Parkinson's disease 6 | 126 | 68 | 1 | ameliorates | Parkinson's disease 6 | 87 | -- | -- | exacerbates | Parkinson's disease 6 | 22 | -- | -- | for disease ribbon | Parkinson's disease 6 | -- | 1 | -- | model of | Parkinson's disease 6 | 18 | 1 | -- |
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Relationships