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General Information
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| Term |
Parkinson's disease 22 |
ID (Ontology) |
DOID:0080504 (Human Disease) |
| Definition |
A late onset Parkinson's disease that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the coiled-coil-helix-coiled-coil-helix domain containing 2 gene on chromosome 7p11.2. |
| Also Known As |
"autosomal dominant Parkinson's disease 22" |
| Comment |
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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 | 7 | | 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 22 | 8 | 5 | 1 | ameliorates | Parkinson's disease 22 | 1 | -- | -- | exacerbates | Parkinson's disease 22 | 1 | -- | -- | for disease ribbon | Parkinson's disease 22 | -- | 2 | -- | model of | Parkinson's disease 22 | 6 | 2 | -- |
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Relationships