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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:Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis
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Accession:DOID:9004166 term browser browse the term
Synonyms:primary_id: MESH:C563479
 alt_id: OMIM:166910


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21128
    physical disorder 4950
      congenital hemolytic anemia 347
        hereditary elliptocytosis 10
          Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis 0
Path 2
Term Annotations click to browse term
  disease 21128
    disease of anatomical entity 18211
      Hemic and Lymphatic Diseases 3853
        hematopoietic system disease 3344
          anemia 778
            normocytic anemia 416
              hemolytic anemia 416
                congenital hemolytic anemia 347
                  hereditary elliptocytosis 10
                    Ovalocytosis, Hereditary Hemolytic, with Defective Erythropoiesis 0
paths to the root