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ONTOLOGY REPORT - ANNOTATIONS


Term:Fanconi anemia complementation group V
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Accession:DOID:0111080 term browser browse the term
Definition:A Fanconi anemia that has_material_basis_in homozygous mutation in the MAD2L2 gene on chromosome 1p36. (DO)
Synonyms:exact_synonym: FANCV;   Fanconi anemia of complementation group V
 primary_id: OMIM:617243
 alt_id: RDO:9001743
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Fanconi anemia complementation group V term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Mad2l2 mitotic arrest deficient 2 like 2 JBrowse link 5 164,943,183 164,956,255 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15619
    Nutritional and Metabolic Diseases 4374
      disease of metabolism 4374
        DNA Repair-Deficiency Disorders 202
          Fanconi anemia 43
            Fanconi anemia complementation group V 1
Path 2
Term Annotations click to browse term
  disease 15619
    disease of anatomical entity 14948
      Hemic and Lymphatic Diseases 0
        hematopoietic system disease 1451
          bone marrow disease 402
            aplastic anemia 150
              congenital hypoplastic anemia 104
                Fanconi anemia 43
                  Fanconi anemia complementation group V 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.