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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:Hemoglobin SC Disease
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Accession:DOID:9006672 term browser browse the term
Definition:One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle cell anemia.
Synonyms:exact_synonym: Hb SC disease;   Hb-S/Hb-C disease;   SC disease;   SC diseases;   hemoglobin SC diseases;   sickle cell hemoglobin C disease
 primary_id: MESH:D006450
 xref: EFO:1001797



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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17996
    physical disorder 4917
      congenital hemolytic anemia 337
        sickle cell anemia 43
          Hemoglobin SC Disease 0
Path 2
Term Annotations click to browse term
  disease 17996
    disease of anatomical entity 15260
      Hemic and Lymphatic Diseases 3704
        hematopoietic system disease 3221
          anemia 753
            normocytic anemia 407
              hemolytic anemia 407
                congenital hemolytic anemia 337
                  hemoglobinopathy 227
                    sickle cell anemia 43
                      Hemoglobin SC Disease 0
paths to the root