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RGD uses the Human Disease Ontology (DO, 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 Ataxia with Dysmorphism
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Accession:DOID:9005852 term browser browse the term
Synonyms:primary_id: MESH:C564802
 alt_id: OMIM:271270
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 12641
    Pathological Conditions, Signs and Symptoms 7581
      Pathologic Processes 5583
        Disease Attributes 566
          Facies 258
            Spinocerebellar Ataxia with Dysmorphism 0
Path 2
Term Annotations click to browse term
  disease 12641
    disease of anatomical entity 12177
      nervous system disease 9943
        central nervous system disease 8423
          brain disease 7795
            movement disease 1076
              Dyskinesias 813
                Ataxia 364
                  Spinocerebellar Ataxias 277
                    Spinocerebellar Ataxia with Dysmorphism 0
paths to the root


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