FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term episodic ataxia ID (Ontology) DOID:963 (Human Disease)
Definition A hereditary ataxia characterized by sporadic bouts of ataxia with or without continuous muscle movement.
Also Known As "Isaacs syndrome"
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
Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 episodic ataxia       --       1
 for disease ribbon | Pelger-Huet anomaly       1       --
 model of | Pelger-Huet anomaly       1       --
Spanning Tree (Parents/Children)
Only view relationship: 
  neurodegenerative disease
   |__hereditary ataxia
       |__episodic ataxia  28 rec.
           |__episodic ataxia type 1 3 rec.
           |__episodic ataxia type 2 1 rec.
           |__episodic ataxia type 3
           |__episodic ataxia type 4
           |__episodic ataxia type 5 1 rec.
           |__episodic ataxia type 6 21 rec.
           |__episodic ataxia type 7
           |__episodic ataxia type 8
           |__episodic ataxia type 9 1 rec.
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Is a hereditary ataxia
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Synonyms
  • "Isaacs syndrome" EXACT
Secondary IDs
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GARD:9851
MESH:C580065
ORDO:211062
SNOMEDCT_US_2023_03_01:421455009
UMLS_CUI:C1720189