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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:Purpura Simplex
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Accession:DOID:9008319 term browser browse the term
Synonyms:exact_synonym: Hereditary familial purpura simplex
 primary_id: MESH:C536249
 alt_id: OMIM:179000



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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18301
    Pathological Conditions, Signs and Symptoms 12359
      Signs and Symptoms 10135
        Skin Manifestations 133
          purpura 57
            Purpura Simplex 0
Path 2
Term Annotations click to browse term
  disease 18301
    disease of anatomical entity 15631
      Hemic and Lymphatic Diseases 3776
        hematopoietic system disease 3274
          blood coagulation disease 945
            hemorrhagic disease 899
              purpura 57
                Purpura Simplex 0
paths to the root