Primary T-lymphocyte immune abnormalities

Symptom Information:

Symptom ID: HPO:0005402
Synonyms:
Primary T-lymphocyte immune abnormalities [OMIM:Primary T-lymphocyte immune abnormalities]
Quality:
Cross references:
OMIM: "Primary T-lymphocyte immune abnormalities" [OMIM:Primary T-lymphocyte immune abnormalities]
Is a (Direct Parents):
HPO         Abnormality of T cell physiology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       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)
                         Primary T-lymphocyte immune abnormalities(HPO:0005402)
       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)
                      Primary T-lymphocyte immune abnormalities(HPO:0005402)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

IMMUNODEFICIENCY, X-LINKED, WITH DEFICIENCY OF 115,000 DALTON SURFACEGLYCOPROTEIN (OMIM:308220)