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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 type dermatomyositis
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Accession:DOID:14203 term browser browse the term
Synonyms:exact_synonym: childhood Dermatomyositis;   childhood type dermatomyositides;   juvenile dermatomyositis;   juvenile myositis
 primary_id: MESH:C000598745
 alt_id: RDO:0016020
 xref: EFO:0000557;   ICD10CM:M33.0;   NCI:C27576
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 18969
    sensory system disease 6961
      skin disease 3968
        dermatomyositis 38
          childhood type dermatomyositis 0
Path 2
Term Annotations click to browse term
  disease 18969
    disease of anatomical entity 18249
      nervous system disease 14091
        peripheral nervous system disease 4124
          neuropathy 3907
            neuromuscular disease 3059
              muscular disease 2148
                muscle tissue disease 1294
                  myopathy 1008
                    myositis 88
                      polymyositis 43
                        dermatomyositis 38
                          childhood type dermatomyositis 0
paths to the root