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ONTOLOGY REPORT - ANNOTATIONS


Term:Fanconi anemia complementation group O
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Accession:DOID:0111096 term browser browse the term
Definition:A Fanconi anemia that has_material_basis_in homozygous mutation in the RAD51C gene on chromosome 17q21-q24. (DO)
Synonyms:exact_synonym: FANCO
 primary_id: OMIM:613390
 alt_id: RDO:0015803
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Fanconi anemia complementation group O term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rad51c RAD51 paralog C JBrowse link 10 74,697,713 74,724,004 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15603
    Nutritional and Metabolic Diseases 4390
      disease of metabolism 4390
        DNA Repair-Deficiency Disorders 202
          Fanconi anemia 43
            Fanconi anemia complementation group O 1
Path 2
Term Annotations click to browse term
  disease 15603
    disease of anatomical entity 14934
      Hemic and Lymphatic Diseases 1724
        hematopoietic system disease 1452
          bone marrow disease 403
            aplastic anemia 150
              congenital hypoplastic anemia 104
                Fanconi anemia 43
                  Fanconi anemia complementation group O 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.