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ONTOLOGY REPORT - ANNOTATIONS


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;   RDO:0001749
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 15619
    disease of anatomical entity 14948
      hematopoietic system disease 1451
        blood coagulation disease 468
          purpura 53
            Purpura Simplex 0
Path 2
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      Hemic and Lymphatic Diseases 1723
        hematopoietic system disease 1451
          blood coagulation disease 468
            hemorrhagic disease 456
              purpura 53
                Purpura Simplex 0
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.