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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:Familial Neurocardiogenic Syncope
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Accession:DOID:9002618 term browser browse the term
Synonyms:exact_synonym: Familial vasovagal syncope
 primary_id: MESH:C536849;   RDO:0002559
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 17129
    disease of anatomical entity 16476
      nervous system disease 12074
        Neurologic Manifestations 5408
          Orthostatic Intolerance 11
            Vasovagal Syncope 1
              Familial Neurocardiogenic Syncope 0
Path 2
Term Annotations click to browse term
  disease 17129
    disease of anatomical entity 16476
      nervous system disease 12074
        central nervous system disease 10353
          brain disease 9712
            disease of mental health 7022
              cognitive disorder 1949
                Consciousness Disorders 23
                  Unconsciousness 23
                    Syncope 10
                      Vasovagal Syncope 1
                        Familial Neurocardiogenic Syncope 0
paths to the root