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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:Feigenbaum Bergeron Richardson Syndrome
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Accession:DOID:9004549 term browser browse the term
Synonyms:primary_id: MESH:C536178;   RDO:0001653
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 16123
    syndrome 7053
      Feigenbaum Bergeron Richardson Syndrome 0
Path 2
Term Annotations click to browse term
  disease 16123
    disease of anatomical entity 15370
      nervous system disease 10975
        central nervous system disease 9096
          brain disease 8405
            movement disease 1097
              Dyskinesias 795
                Myoclonus 85
                  Myoclonic Epilepsies 80
                    Feigenbaum Bergeron Richardson Syndrome 0
paths to the root