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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.
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: OMIM:183100


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17774
    syndrome 10062
      multiple system atrophy 41
        olivopontocerebellar atrophy 22
          Spinocerebellar Atrophy with Pupillary Paralysis 0
Path 2
Term Annotations click to browse term
  disease 17774
    disease of anatomical entity 15146
      nervous system disease 13207
        central nervous system disease 11844
          brain disease 11124
            movement disease 2494
              multiple system atrophy 41
                olivopontocerebellar atrophy 22
                  Spinocerebellar Atrophy with Pupillary Paralysis 0
paths to the root