FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term synucleinopathy ID (Ontology) DOID:0050890 (Human Disease)
Definition A neurodegenerative disease that is characterized by the abnormal accumulation of aggregates of alpha-synuclein protein in neurons, nerve fibres or glial cells.
Also Known As "alpha Synucleinopathies" ; "Synucleinopathies"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
Records annotated with this exact term (annotations to child terms are NOT included)
Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS      17
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Alleles Genes
 synucleinopathy      18      9
 ameliorates | synucleinopathy       7       --
 exacerbates | synucleinopathy       2       --
 model of | synucleinopathy       9       --
Spanning Tree (Parents/Children)
Only view relationship:
  central nervous system disease
   |__neurodegenerative disease
       |__synucleinopathy  1223 rec.
           |__multiple system atrophy 4 rec.
           |   |__striatal degeneration 2 1 rec.
           |   |__striatonigral degeneration 3 rec.
           |__Parkinson's disease 1205 rec.
               |__early-onset Parkinson's disease(+) 329 rec.
               |__late onset Parkinson's disease(+) 407 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a neurodegenerative disease
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "alpha Synucleinopathies" EXACT
    "Synucleinopathies" EXACT
Secondary IDs
hide External Crossreferences & Linkouts