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ectodermal dysplasia and immunodeficiency 1 - Ontology Report - Rat Genome Database

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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:ectodermal dysplasia and immunodeficiency 1
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Accession:DOID:0081078 term browser browse the term
Definition:An ectodermal dysplasia and immunodeficiency that is characterized by onset of recurrent severe infections due to immunodeficiency in early infancy or in the first years of life and that has_material_basis_in hemizygous mutation in the IKK-gamma gene (IKBKG) on chromosome Xq28. (DO)
Synonyms:exact_synonym: EDAID1;   OLEDAID;   X-linked hyper-IgM immunodeficiency with hypohidrotic ectodermal dysplasia;   XHM-ED;   anhidrotic ectodermal dysplasia with immunodeficiency, osteopetrosis, and lymphedema
 alt_id: DOID:9005011
 xref: MESH:C564538;   MESH:C564542;   MIM:300291;   MONDO:0020740;   NCI:C118844;   ORDO:69088


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ectodermal dysplasia and immunodeficiency 1 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G G6PD glucose-6-phosphate dehydrogenase ISO ClinVar Annotator: match by term: Hyper-IgM immunodeficiency, X-linked, with hypohidrotic ectodermal dysplasia ClinVar PMID:25741868 NCBI chr  X:128,768,028...128,788,366
Ensembl chr  X:128,770,268...128,786,961
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G LOC103232832 inhibitor of nuclear factor kappa B kinase regulatory subunit gamma ISO ClinVar Annotator: match by term: Ectodermal dysplasia and immunodeficiency 1 | ClinVar Annotator: match by term: Hyper-IgM immunodeficiency, X-linked, with hypohidrotic ectodermal dysplasia OMIM
ClinVar
PMID:117248 PMID:8169255 PMID:11047757 PMID:11179023 PMID:11224521 More... NCBI chr  X:128,781,975...128,816,039
Ensembl chr  X:128,787,785...128,806,083
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15628
    syndrome 10613
      primary immunodeficiency disease 4088
        ectodermal dysplasia and immune deficiency 9
          ectodermal dysplasia and immunodeficiency 1 2
Path 2
Term Annotations click to browse term
  disease 15628
    Pathological Conditions, Signs and Symptoms 12193
      Signs and Symptoms 10273
        Neurologic Manifestations 9954
          sensory system disease 7007
            mouth disease 994
              tooth disease 450
                Tooth Abnormalities 295
                  tooth agenesis 85
                    anodontia 75
                      hypohidrotic ectodermal dysplasia 26
                        ectodermal dysplasia and immune deficiency 9
                          ectodermal dysplasia and immunodeficiency 1 2
paths to the root