Reduced delayed hypersensitivity

Symptom Information:

Symptom ID: HPO:0002972
Synonyms:
Decreased reactivity to skin test antigens [HPO:0002972]
Deficiency of delayed skin hypersensitivity [HPO:0002972]
Impaired delayed hypersensitivity [HPO:0002972]
Decreased reactivity to skin test antigens [OMIM:Decreased reactivity to skin test antigens]
Deficiency of delayed skin hypersensitivity [OMIM:Deficiency of delayed skin hypersensitivity]
Impaired delayed hypersensitivity [OMIM:Impaired delayed hypersensitivity]
Reduced delayed hypersensitivity [OMIM:Reduced delayed hypersensitivity]
Quality:
Cross references:
OMIM: "Decreased reactivity to skin test antigens" [OMIM:Decreased reactivity to skin test antigens]
OMIM: "Deficiency of delayed skin hypersensitivity" [OMIM:Deficiency of delayed skin hypersensitivity]
OMIM: "Impaired delayed hypersensitivity" [OMIM:Impaired delayed hypersensitivity]
OMIM: "Reduced delayed hypersensitivity" [OMIM:Reduced delayed hypersensitivity]
Is a (Direct Parents):
HPO         Abnormal delayed hypersensitivity skin test
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)
                         Abnormal delayed hypersensitivity skin test(HPO:0002963)
                            Reduced delayed hypersensitivity(HPO:0002972)
       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)
                      Abnormal delayed hypersensitivity skin test(HPO:0002963)
                         Reduced delayed hypersensitivity(HPO:0002972)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME (OMIM:601859)
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE IIA (OMIM:603909)
Autoimmune lymphoproliferative syndrome (Orphanet:3261)
COMBINED INFLAMMATORY AND IMMUNOLOGIC DEFECT (OMIM:216920)
Griscelli disease type 2 (Orphanet:79477)
RETINAL TELANGIECTASIA AND HYPOGAMMAGLOBULINEMIA (OMIM:267900)
Thymic aplasia (Orphanet:83471)