Absent cellular immunity

Symptom Information:

Symptom ID: HPO:0005354
Synonyms:
Cellular immune deficiency [Orphanet:47320]
T-lymphocyte deficiency (finding) [Orphanet:47320]
T-lymphocyte deficiency [Orphanet:47320]
Absent cellular immunity [OMIM:Absent cellular immunity]
T-cell deficiency/cellular immunity deficiency [Orphanet:47320]
T-lymphocyte deficiency [OMIM:T-lymphocyte deficiency]
Quality:
Cross references:
HPO:0005374 "Cellular immunodeficiency" [Orphanet:47320]
HPO:0002843 "Abnormality of T cells" [Orphanet:47320]
HPO:0005352 "Severe T-cell immunodeficiency" [Orphanet:47320]
Orphanet:47320 "T-cell deficiency/cellular immunity deficiency" [Orphanet:47320]
OMIM: "Absent cellular immunity" [OMIM:Absent cellular immunity]
OMIM: "T-lymphocyte deficiency" [OMIM:T-lymphocyte deficiency]
UMLS:C1744558 "T-lymphocyte deficiency" [Orphanet:47320]
Is a (Direct Parents):
HPO         Abnormality of T cell physiology
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 T cell physiology(HPO:0011840)
                      Absent cellular immunity(HPO:0005354)
       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)
                         Absent cellular immunity(HPO:0005354)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
Reticular dysgenesis (Orphanet:33355)