Abnormality of T cells

Symptom Information:

Symptom ID: HPO:0002843
Synonyms:
Cellular immune defect [HPO:0002843]
Defective cellular immunity [HPO:0002843]
Cellular immune deficiency [Orphanet:47320]
T-lymphocyte deficiency (finding) [Orphanet:47320]
T-lymphocyte deficiency [Orphanet:47320]
Cellular immune defect [OMIM:Cellular immune defect]
Defective cellular immunity [OMIM:Defective cellular immunity]
T-cell deficiency/cellular immunity deficiency [Orphanet:47320]
T-lymphocyte deficiency [OMIM:T-lymphocyte deficiency]
Quality:
Cross references:
HPO:0005354 "Absent cellular immunity" [Orphanet:47320]
HPO:0005374 "Cellular immunodeficiency" [Orphanet:47320]
HPO:0005352 "Severe T-cell immunodeficiency" [Orphanet:47320]
Orphanet:47320 "T-cell deficiency/cellular immunity deficiency" [Orphanet:47320]
OMIM: "Cellular immune defect" [OMIM:Cellular immune defect]
OMIM: "Defective cellular immunity" [OMIM:Defective cellular immunity]
OMIM: "T-lymphocyte deficiency" [OMIM:T-lymphocyte deficiency]
UMLS:C1744558 "T-lymphocyte deficiency" [Orphanet:47320]
Is a (Direct Parents):
HPO         Abnormality of lymphocytes
HPO         Abnormal T cell morphology
Orphanet Recurrent bacterial infections
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 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)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME (OMIM:215250)
LYMPHOID SYSTEM DETERIORATION, PROGRESSIVE (OMIM:247630)
OKT4 EPITOPE DEFICIENCY (OMIM:613949)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Thymic aplasia (Orphanet:83471)