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 8 ID (Ontology) DOID:0060371 (Human Disease)
Definition A late onset Parkinson's disease that has_material_basis_in heterozygous mutation in the dardarin encoding gene on chromosome 12q12.
Also Known As "autosomal dominant Parkinson disease 8" ; "autosomal dominant Parkinson's disease 8"
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS      69
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 Parkinson's disease 8      71     29      1
 ameliorates | Parkinson's disease 8      24       --       --
 exacerbates | Parkinson's disease 8      16       --       --
 for disease ribbon | Parkinson's disease 8       --       1       --
 model of | Parkinson's disease 8      30      1       --
 DOES NOT model | Parkinson's disease 8       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 8  101 rec.
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Is a autosomal dominant disease
late onset Parkinson's disease
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Synonyms
  • "autosomal dominant Parkinson disease 8" EXACT
    "autosomal dominant Parkinson's disease 8" EXACT
Secondary IDs
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MIM:607060