FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Parkinson's disease 17 ID (Ontology) DOID:0060897 (Human Disease)
Definition A late-onset Parkinson disease that has_material_basis_in heterozygous mutation in the VPS35 gene on chromosome 16q13.
Also Known As "autosomal dominant Parkinson disease 17" ; "Parkinson disease 17"
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DO.org
Annotations
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       1
Human Disease Models (FBhh)  DOID       1
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 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes Human Disease Models
 Parkinson's disease 17       1      2      1
 for disease ribbon | Parkinson's disease 17       --       1       --
 model of | Parkinson's disease 17       1      1       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease______
Parkinson's disease                 |
 |__late onset Parkinson's disease__|
                                    Parkinson's disease 17  4 rec.
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Is a autosomal dominant disease
late onset Parkinson's disease
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Synonyms
  • "autosomal dominant Parkinson disease 17" EXACT
    "Parkinson disease 17" EXACT
Secondary IDs
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MIM:614203