Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

ONTOLOGY REPORT - ANNOTATIONS


Term:Common Variable Immunodeficiency 12
go back to main search page
Accession:DOID:9008356 term browser browse the term
Definition:An autosomal dominant primary immunodeficiency characterized by recurrent infections, mainly respiratory, associated with hypogammaglobulinemia. (OMIM)
Synonyms:exact_synonym: CVID12;   NFKB1 DEFICIENCY
 primary_id: OMIM:616576;   RDO:9001616
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
Common Variable Immunodeficiency 12 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nfkb1 nuclear factor kappa B subunit 1 JBrowse link 2 240,773,520 240,890,053 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15639
    syndrome 5218
      primary immunodeficiency disease 957
        common variable immunodeficiency 42
          Common Variable Immunodeficiency 12 1
Path 2
Term Annotations click to browse term
  disease 15639
    disease of anatomical entity 14969
      Immune & Inflammatory Diseases 3103
        immune system disease 2524
          primary immunodeficiency disease 957
            lymphoproliferative syndrome 605
              agammaglobulinemia 55
                common variable immunodeficiency 42
                  Common Variable Immunodeficiency 12 1
paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.