FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term progressive supranuclear palsy ID (Ontology) DOID:678 (Human Disease)
Definition A movement disease that is characterized by serious and progressive problems with control of gait and balance, along with complex eye movement and thinking problems. It involves gradual deterioration and death of specific volumes of the brain.
Also Known As "progressive supranuclear ophthalmoplegia" ; "Steele-Richardson-Olszewski syndrome"
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Data Class Field Records
Alleles (FBal)  HUMAN_DISEASE_INTERACTIONS       4
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 progressive supranuclear palsy       4      2      1
 for disease ribbon | progressive supranuclear palsy       --       1       --
 model of | progressive supranuclear palsy       4      1       --
Spanning Tree (Parents/Children)
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  brain disease
   |__movement disease
       |__progressive supranuclear palsy  7 rec.
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Is a movement disease
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Synonyms
  • "progressive supranuclear ophthalmoplegia" EXACT
    "Steele-Richardson-Olszewski syndrome" EXACT
Secondary IDs
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GARD:7471
ICD10CM:G23.1
MESH:D013494
MIM:601104
MIM:609454
MIM:610898
NCI:C85028
ORDO:683
SNOMEDCT_US_2023_03_01:192975003
UMLS_CUI:C0038868