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juvenile myoclonic epilepsy 3 - Ontology Report - Rat Genome Database

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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:juvenile myoclonic epilepsy 3
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Accession:DOID:0111326 term browser browse the term
Definition:A juvenile myoclonic epilepsy that has_material_basis_in variation in a region on chromosome 6p21. (DO)
Synonyms:exact_synonym: EJM3;   MYOCLONIC EPILEPSY, JUVENILE, SUSCEPTIBILITY TO, 3
 primary_id: MIM:608816

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Path 1
Term Annotations click to browse term
  disease 288179
    syndrome 133013
      electroclinical syndrome 15195
        absence epilepsy 2422
          adolescence-adult electroclinical syndrome 1359
            juvenile myoclonic epilepsy 137
              juvenile myoclonic epilepsy 3 0
Path 2
Term Annotations click to browse term
  disease 288179
    disease of anatomical entity 271815
      nervous system disease 190640
        central nervous system disease 157774
          brain disease 148547
            epilepsy 29636
              electroclinical syndrome 15195
                absence epilepsy 2422
                  adolescence-adult electroclinical syndrome 1359
                    juvenile myoclonic epilepsy 137
                      juvenile myoclonic epilepsy 3 0
paths to the root