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Term:spinocerebellar ataxia type 2
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Accession:DOID:0050955 term browser browse the term
Definition:An autosomal dominant cerebellar ataxia that is characterized by ataxia, bulbar palsy, peripheral neuropathy chorea and muscle atrophy, has_material_basis_in mutation in the ATXN2 gene. (DO)
Synonyms:exact_synonym: OPCA2;   SCA2;   olivopontocerebellar atrophy 2;   olivopontocerebellar atrophy II;   olivopontocerebellar atrophy, Holguin type;   spinocerebellar ataxia 2;   spinocerebellar ataxia with slow eye movements;   spinocerebellar ataxia, Cuban type;   spinocerebellar atrophy 2;   spinocerebellar atrophy II;   spinocerebellar degeneration with slow eye movements
 primary_id: OMIM:183090
 alt_id: RDO:9003726
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spinocerebellar ataxia type 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Atxn2 ataxin 2 JBrowse link 12 40,264,601 40,335,637 RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15502
    syndrome 5379
      multiple system atrophy 29
        olivopontocerebellar atrophy 10
          spinocerebellar ataxia type 2 1
Path 2
Term Annotations click to browse term
  disease 15502
    disease of anatomical entity 14856
      nervous system disease 10270
        central nervous system disease 8409
          brain disease 7762
            movement disease 1010
              Dyskinesias 717
                Ataxia 309
                  Spinocerebellar Ataxias 201
                    cerebellar ataxia 174
                      autosomal dominant cerebellar ataxia 64
                        spinocerebellar ataxia type 2 1
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