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ONTOLOGY REPORT - ANNOTATIONS


Term:Spinocerebellar Atrophy with Pupillary Paralysis
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Accession:DOID:9003187 term browser browse the term
Synonyms:primary_id: MESH:C566668
 alt_id: RDO:0014964
For additional species annotation, visit the Alliance of Genome Resources.


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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 Atrophy with Pupillary Paralysis 0
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
              multiple system atrophy 29
                olivopontocerebellar atrophy 10
                  Spinocerebellar Atrophy with Pupillary Paralysis 0
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.