ONTOLOGY REPORT - ANNOTATIONS


Term:Fanconi anemia complementation group B
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Accession:DOID:0111098 term browser browse the term
Definition:A Fanconi anemia that has_material_basis_in mutation in the FANCB gene on chromosome Xp22. (DO)
Synonyms:exact_synonym: FA2;   FACB;   FANCB;   Fanconi Pancytopenia, Type 2
 primary_id: MESH:C564497;   RDO:0013442
 alt_id: OMIM:300514
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Fanconi anemia complementation group B term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fancb FA complementation group B JBrowse link X 31,124,018 31,140,790 RGD:7240710
RGD:8554872

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  disease 14919
    Nutritional and Metabolic Diseases 4263
      disease of metabolism 4263
        DNA Repair-Deficiency Disorders 179
          Fanconi anemia 43
            Fanconi anemia complementation group B 1
Path 2
Term Annotations click to browse term
  disease 14919
    disease of anatomical entity 14083
      Hemic and Lymphatic Diseases 1590
        hematopoietic system disease 1374
          bone marrow disease 398
            aplastic anemia 146
              congenital hypoplastic anemia 102
                Fanconi anemia 43
                  Fanconi anemia complementation group B 1
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