FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term hereditary ataxia ID (Ontology) DOID:0050951 (Human Disease)
Definition A neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements.
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DO.org
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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       5
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Alleles Genes Human Disease Models
 hereditary ataxia       5      3      1
 ameliorates | hereditary ataxia       1       --       --
 model of | hereditary ataxia       4       --       --
Spanning Tree (Parents/Children)
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  central nervous system disease
   |__neurodegenerative disease
       |__hereditary ataxia  1254 rec.
           |__autosomal dominant sensory ataxia 1
           |__cerebellar ataxia 1092 rec.
           |   |__autosomal dominant cerebellar ataxia(+) 895 rec.
           |   |__autosomal recessive cerebellar ataxia(+) 209 rec.
           |__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.
           |__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.
           |__X-linked hereditary ataxia 130 rec.
               |__fragile X-associated tremor/ataxia syndrome 129 rec.
               |__X-linked cerebellar ataxia(+) 1 rec.
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GARD:6614