T lymphocytopenia

Symptom Information:

Symptom ID: HPO:0005403
Synonyms:
Decreased numbers of circulating T cells [HPO:0005403]
Low T cell count [HPO:0005403]
Reduced number of T cells [HPO:0005403]
Decreased numbers of circulating T cells [OMIM:Decreased numbers of circulating T cells]
Low T cell count [OMIM:Low T cell count]
Reduced number of T cells [OMIM:Reduced number of T cells]
Reduced numbers of T cells [OMIM:Reduced numbers of T cells]
Quality:
Cross references:
OMIM: "Decreased numbers of circulating T cells" [OMIM:Decreased numbers of circulating T cells]
OMIM: "Low T cell count" [OMIM:Low T cell count]
OMIM: "Reduced number of T cells" [OMIM:Reduced number of T cells]
OMIM: "Reduced numbers of T cells" [OMIM:Reduced numbers of T cells]
Is a (Direct Parents):
HPO         Abnormality of T cell number
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of leukocytes(HPO:0001881)
             Abnormality of lymphocytes(HPO:0004332)
                Abnormality of T cells(HPO:0002843)
                   Abnormality of T cell number(HPO:0011839)
                      T lymphocytopenia(HPO:0005403)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of cellular immune system(HPO:0010987)
             Abnormality of leukocytes(HPO:0001881)
                Abnormality of lymphocytes(HPO:0004332)
                   Abnormality of T cells(HPO:0002843)
                      Abnormality of T cell number(HPO:0011839)
                         T lymphocytopenia(HPO:0005403)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

ATAXIA-TELANGIECTASIA (OMIM:208900)
Combined immunodeficiency with skin granulomas (Orphanet:157949)
ICF syndrome (Orphanet:2268)
IMMUNODEFICIENCY 25 (OMIM:610163)
IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTSAND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES (OMIM:242870)
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME1 (OMIM:242860)
Immunodeficiency due to CD25 deficiency (Orphanet:169100)
Nijmegen breakage syndrome (Orphanet:647)
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION (OMIM:607944)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)