Cellular immunodeficiency

Symptom Information:

Symptom ID: HPO:0005374
Synonyms:
Cellular immune deficiency [Orphanet:47320]
T-lymphocyte deficiency (finding) [Orphanet:47320]
T-lymphocyte deficiency [Orphanet:47320]
Cellular immunodeficiency [OMIM:Cellular immunodeficiency]
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: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: "Cellular immunodeficiency" [OMIM:Cellular immunodeficiency]
OMIM: "T-lymphocyte deficiency" [OMIM:T-lymphocyte deficiency]
UMLS:C1744558 "T-lymphocyte deficiency" [Orphanet:47320]
Is a (Direct Parents):
Orphanet Recurrent bacterial infections
HPO         Immunodeficiency
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Immunodeficiency(HPO:0002721)
                Cellular immunodeficiency(HPO:0005374)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
Cartilage-hair hypoplasia (Orphanet:175)
LEUKEMIA, CHRONIC LYMPHOCYTIC (OMIM:151400)
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION (OMIM:607944)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)