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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 17415
    Pathological Conditions, Signs and Symptoms 11801
      Signs and Symptoms 9739
        Skin Manifestations 121
          purpura 47
            Purpura Simplex 0
Path 2
Term Annotations click to browse term
  disease 17415
    disease of anatomical entity 14875
      Hemic and Lymphatic Diseases 3611
        hematopoietic system disease 3134
          blood coagulation disease 893
            hemorrhagic disease 850
              purpura 47
                Purpura Simplex 0
paths to the root