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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:Congenital Torticollis
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Accession:DOID:9008633 term browser browse the term
Synonyms:exact_synonym: Congenital muscular torticollis;   Familial spasmodic torticollis;   Familial torticollis
 primary_id: MESH:C535425;   RDO:0000528
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 12528
    disease of anatomical entity 12209
      nervous system disease 10127
        Neurologic Manifestations 4698
          Dyskinesias 814
            dystonia 169
              focal dystonia 9
                cervical dystonia 3
                  Congenital Torticollis 0
Path 2
Term Annotations click to browse term
  disease 12528
    disease of anatomical entity 12209
      nervous system disease 10127
        central nervous system disease 8880
          brain disease 8337
            movement disease 1089
              Dyskinesias 814
                dystonia 169
                  focal dystonia 9
                    cervical dystonia 3
                      Congenital Torticollis 0
paths to the root