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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:Childhood Absence Epilepsy 2
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Accession:DOID:9009061 term browser browse the term
Synonyms:exact_synonym: ECA2
 broad_synonym: GABRG2-RELATED DISORDER
 related_synonym: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
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 16103
    syndrome 6989
      electroclinical syndrome 393
        absence epilepsy 113
          childhood electroclinical syndrome 76
            childhood absence epilepsy 38
              Childhood Absence Epilepsy 2 1
Path 2
Term Annotations click to browse term
  disease 16103
    disease of anatomical entity 15351
      nervous system disease 10863
        central nervous system disease 9005
          brain disease 8328
            epilepsy 1481
              electroclinical syndrome 393
                absence epilepsy 113
                  childhood electroclinical syndrome 76
                    childhood absence epilepsy 38
                      Childhood Absence Epilepsy 2 1
paths to the root

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