FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term spinocerebellar ataxia type 19/22 ID (Ontology) DOID:0050970 (Human Disease)
Definition An autosomal dominant cerebellar ataxia that is characterized by mild cerebellar ataxia, cognitive impairment, myoclonus and tremor.
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 spinocerebellar ataxia type 19/22       1      1
 for disease ribbon | spinocerebellar ataxia type 19/22       1       --
 model of | spinocerebellar ataxia type 19/22       1       --
Spanning Tree (Parents/Children)
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autosomal dominant disease__
cerebellar ataxia___________|
                            autosomal dominant cerebellar ataxia
                             |__spinocerebellar ataxia type 19/22  2 rec.
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Is a autosomal dominant cerebellar ataxia
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Synonyms
Secondary IDs
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GARD:12365
MIM:607346