Impaired T cell function

Symptom Information:

Symptom ID: HPO:0005435
Synonyms:
T-cell dysfunction [HPO:0005435]
Impaired T cell function [OMIM:Impaired T cell function]
T-cell dysfunction [OMIM:T-cell dysfunction]
T cell dysfunction [OMIM:T cell dysfunction]
T-cell dysfunction (1 patient) [OMIM:T-cell dysfunction (1 patient)]
Quality:
Cross references:
OMIM: "Impaired T cell function" [OMIM:Impaired T cell function]
OMIM: "T-cell dysfunction" [OMIM:T-cell dysfunction]
OMIM: "T cell dysfunction" [OMIM:T cell dysfunction]
OMIM: "T-cell dysfunction (1 patient)" [OMIM:T-cell dysfunction (1 patient)]
Is a (Direct Parents):
HPO         Abnormality of T cell physiology
HPO         Defective T cell proliferation
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 physiology(HPO:0011840)
                      Impaired T cell function(HPO:0005435)
       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 physiology(HPO:0011840)
                         Impaired T cell function(HPO:0005435)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl (OMIM:614576)
Hereditary orotic aciduria (Orphanet:30)
IMMUNODEFICIENCY, COMMON VARIABLE, 1 (OMIM:607594)
IMMUNODEFICIENCY, COMMON VARIABLE, 2 (OMIM:240500)
Progeria - short stature - pigmented nevi (Orphanet:2959)
T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY (OMIM:615387)
VELOCARDIOFACIAL SYNDROME (OMIM:192430)