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

ONTOLOGY REPORT - ANNOTATIONS


Term:Immunodeficiency 27B
go back to main search page
Accession:DOID:9002259 term browser browse the term
Definition:An autosomal dominant IFNGR1 deficiency that commonly features recurrent, moderately severe infections with environmental mycobacteria or bacillus Calmette-Guerin (BCG). (OMIM)
Synonyms:exact_synonym: IFNGR1 DEFICIENCY, AUTOSOMAL DOMINANT;   IMD27B;   IMMUNODEFICIENCY 27B, MYCOBACTERIOSIS, AUTOSOMAL DOMINANT
 primary_id: OMIM:615978;   RDO:9001313
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants       view all columns           Sort by:
 
Immunodeficiency 27B term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ifngr1 interferon gamma receptor 1 JBrowse link 1 15,062,380 15,080,815 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15553
    syndrome 5224
      primary immunodeficiency disease 978
        Immunodeficiency 27B 1
Path 2
Term Annotations click to browse term
  disease 15553
    disease of anatomical entity 14837
      Immune & Inflammatory Diseases 3120
        immune system disease 2541
          primary immunodeficiency disease 978
            Immunodeficiency 27B 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.