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;   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

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  disease 14920
    Nutritional and Metabolic Diseases 4265
      disease of metabolism 4265
        DNA Repair-Deficiency Disorders 179
          Fanconi anemia 43
            Fanconi anemia complementation group C 2
Path 2
Term Annotations click to browse term
  disease 14920
    disease of anatomical entity 14086
      Hemic and Lymphatic Diseases 1591
        hematopoietic system disease 1375
          bone marrow disease 399
            aplastic anemia 147
              congenital hypoplastic anemia 103
                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.