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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:Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia
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Accession:DOID:9001901 term browser browse the term
Synonyms:primary_id: MESH:C566188
 alt_id: MIM:113610



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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19142
    disease of anatomical entity 18455
      nervous system disease 14362
        neurodegenerative disease 5069
          hereditary ataxia 632
            cerebellar ataxia 482
              Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia 0
Path 2
Term Annotations click to browse term
  disease 19142
    disease of anatomical entity 18455
      nervous system disease 14362
        central nervous system disease 12636
          brain disease 11856
            movement disease 2632
              Dyskinesias 2232
                Ataxia 957
                  hereditary ataxia 632
                    cerebellar ataxia 482
                      Branchial Myoclonus with Spastic Paraparesis and Cerebellar Ataxia 0
paths to the root