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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:Acquired Hypoprothrombinemia
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Accession:DOID:9002296 term browser browse the term
Synonyms:primary_id: MESH:C538174

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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16465
    disease of anatomical entity 14116
      hematopoietic system disease 2989
        blood coagulation disease 860
          Coagulation Protein Disorders 90
            prothrombin deficiency 2
              Acquired Hypoprothrombinemia 0
Path 2
Term Annotations click to browse term
  disease 16465
    Developmental Disease 16381
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 16324
        genetic disease 16311
          monogenic disease 9605
            autosomal genetic disease 8889
              autosomal recessive disease 6216
                prothrombin deficiency 2
                  Acquired Hypoprothrombinemia 0
paths to the root