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 23 ID (Ontology) DOID:0060896 (Human Disease)
Definition An early-onset Parkinson disease that has_material_basis_in homozygous or compound heterozygous mutation in the VPS13C gene on chromosome 15q22.
Also Known As "autosomal recessive early-onset Parkinson disease 23" ; "autosomal recessive early-onset Parkinson's disease 23"
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 Parkinson's disease 23       1      1
 for disease ribbon | Parkinson's disease 23       1       --
 model of | Parkinson's disease 23       1       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease______
Parkinson's disease                  |
 |__early-onset Parkinson's disease__|
                                     Parkinson's disease 23  2 rec.
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Is a autosomal recessive disease
early-onset Parkinson's disease
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Synonyms
  • "autosomal recessive early-onset Parkinson disease 23" EXACT
    "autosomal recessive early-onset Parkinson's disease 23" EXACT
Secondary IDs
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ICD10CM:G20
MIM:616840