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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:immunodeficiency 25
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Accession:DOID:0111942 term browser browse the term
Definition:A T cell deficiency characterized by decreased T cell counts, normal B cell counts, and eosinophilia that has_material_basis_in homozygous or compound heterozygous mutation in CD247 on chromosome 1q24.2. (DO)
Synonyms:exact_synonym: IMD25;   immunodeficiency due to defect in CD3-zeta
 primary_id: MESH:C565712
 alt_id: OMIM:610163
For additional species annotation, visit the Alliance of Genome Resources.



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immunodeficiency 25 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cd247 Cd247 molecule ISO ClinVar Annotator: match by term: Immunodeficiency 25 OMIM
ClinVar
PMID:9536098 PMID:16672702 PMID:17170122 PMID:17576681 PMID:25741868 More... NCBI chr13:78,043,302...78,118,437
Ensembl chr13:78,043,307...78,122,263
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18156
    syndrome 9705
      primary immunodeficiency disease 3835
        T cell deficiency 43
          immunodeficiency 25 1
Path 2
Term Annotations click to browse term
  disease 18156
    Developmental Disease 12940
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 11670
        genetic disease 11174
          monogenic disease 8709
            autosomal genetic disease 7745
              autosomal recessive disease 4832
                immunodeficiency 25 1
paths to the root