ONTOLOGY REPORT - ANNOTATIONS


Term:Spinocerebellar Ataxia, Autosomal Recessive 23
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Accession:DOID:9003346 term browser browse the term
Definition:A neurologic disorder characterized by epilepsy, intellectual disability, and gait ataxia. (OMIM)
Synonyms:exact_synonym: SCAR23
 primary_id: OMIM:616949
 alt_id: RDO:9001204
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Spinocerebellar Ataxia, Autosomal Recessive 23 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Tdp2 tyrosyl-DNA phosphodiesterase 2 JBrowse link 17 42,229,667 42,241,025 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14919
    disease of anatomical entity 14083
      nervous system disease 9147
        neurodegenerative disease 2534
          primary cerebellar degeneration 223
            Spinocerebellar Ataxias 205
              Spinocerebellar Ataxia, Autosomal Recessive 23 1
Path 2
Term Annotations click to browse term
  disease 14919
    disease of anatomical entity 14083
      nervous system disease 9147
        central nervous system disease 6945
          brain disease 6451
            movement disease 1005
              Dyskinesias 717
                Ataxia 307
                  Spinocerebellar Ataxias 205
                    Spinocerebellar Ataxia, Autosomal Recessive 23 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.