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ONTOLOGY REPORT - ANNOTATIONS


Term:Immunodeficiency 58
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Accession:DOID:9005311 term browser browse the term
Definition:An autosomal recessive primary immunologic disorder characterized by early-onset skin lesions, including eczematous dermatitis, infectious abscesses, and warts, recurrent respiratory infections or allergies, and chronic persistent infections with candida, Molluscum contagiosum, mycobacteria, EBV, bacteria, and viruses.
Synonyms:exact_synonym: IMD58
 primary_id: OMIM:618131
For additional species annotation, visit the Alliance of Genome Resources.


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Immunodeficiency 58 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Carmil2 capping protein regulator and myosin 1 linker 2 JBrowse link 19 37,652,383 37,665,333 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15502
    syndrome 5379
      primary immunodeficiency disease 988
        Immunodeficiency 58 1
Path 2
Term Annotations click to browse term
  disease 15502
    disease of anatomical entity 14856
      Immune & Inflammatory Diseases 3130
        immune system disease 2548
          primary immunodeficiency disease 988
            Immunodeficiency 58 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.