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ONTOLOGY REPORT - ANNOTATIONS


Term:Common Variable Immunodeficiency 13
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Accession:DOID:9008141 term browser browse the term
Definition:An autosomal dominant primary immunodeficiency disorder characterized by recurrent bacterial infections, mainly affecting the respiratory tract, and associated with hypogammaglobulinemia and decreased numbers of B cells. (OMIM)
Synonyms:exact_synonym: CVID13
 primary_id: OMIM:616873;   RDO:9000373
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Common Variable Immunodeficiency 13 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ikzf1 IKAROS family zinc finger 1 JBrowse link 14 91,782,281 91,867,828 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15608
    syndrome 5790
      primary immunodeficiency disease 993
        common variable immunodeficiency 42
          Common Variable Immunodeficiency 13 1
Path 2
Term Annotations click to browse term
  disease 15608
    disease of anatomical entity 14965
      Immune & Inflammatory Diseases 3226
        immune system disease 2642
          primary immunodeficiency disease 993
            lymphoproliferative syndrome 646
              agammaglobulinemia 55
                common variable immunodeficiency 42
                  Common Variable Immunodeficiency 13 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.