ONTOLOGY REPORT - ANNOTATIONS


Term:Anhidrotic Ectodermal Dysplasia with T-Cell Immunodeficiency, Autosomal Dominant
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Accession:DOID:9000561 term browser browse the term
Synonyms:primary_id: MESH:C567411
 alt_id: OMIM:612132;   RDO:0015489
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Anhidrotic Ectodermal Dysplasia with T-Cell Immunodeficiency, Autosomal Dominant term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nfkbia NFKB inhibitor alpha JBrowse link 6 76,267,227 76,270,457 RGD:7240710
RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14875
    syndrome 4220
      primary immunodeficiency disease 930
        Anhidrotic Ectodermal Dysplasia with T-Cell Immunodeficiency, Autosomal Dominant 1
Path 2
Term Annotations click to browse term
  disease 14875
    disease of anatomical entity 14051
      nervous system disease 9116
        sensory system disease 4246
          skin disease 2253
            Skin Abnormalities 344
              ectodermal dysplasia 142
                hypohidrotic ectodermal dysplasia 9
                  Anhidrotic Ectodermal Dysplasia with T-Cell Immunodeficiency, Autosomal Dominant 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.