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ONTOLOGY REPORT - ANNOTATIONS


Term:Fanconi anemia complementation group C
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Accession:DOID:0111087 term browser browse the term
Definition:A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCC gene on chromosome 9q22. (DO)
Synonyms:exact_synonym: FA3;   FAC;   FACC;   FANCC;   FANCONI PANCYTOPENIA, TYPE 3
 primary_id: OMIM:227645
 alt_id: RDO:0015790
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Fanconi anemia complementation group C term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fancc FA complementation group C JBrowse link 17 826,512 955,703 RGD:7240710
RGD:8554872
G Npepo aminopeptidase O JBrowse link 17 507,389 825,062 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15639
    Nutritional and Metabolic Diseases 4392
      disease of metabolism 4392
        DNA Repair-Deficiency Disorders 202
          Fanconi anemia 43
            Fanconi anemia complementation group C 2
Path 2
Term Annotations click to browse term
  disease 15639
    disease of anatomical entity 14969
      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 C 2
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.