FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term spastic ataxia ID (Ontology) DOID:0050952 (Human Disease)
Definition A hereditary ataxia that is characterized by early onset of cerebellar ataxia, pyramidal tract signs and peripheral neuropathy.
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DO.org
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Human Disease Models
 spastic ataxia       1
Spanning Tree (Parents/Children)
Only view relationship: 
  neurodegenerative disease
   |__hereditary ataxia
       |__spastic ataxia  10 rec.
           |__spastic ataxia 1 1 rec.
           |__spastic ataxia 2 1 rec.
           |__spastic ataxia 3 2 rec.
           |__spastic ataxia 4 2 rec.
           |__spastic ataxia 5 2 rec.
           |__spastic ataxia 7
           |__spastic ataxia 8 1 rec.
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Is a hereditary ataxia
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MESH:C564815