Cutaneous anergy

Symptom Information:

Symptom ID: HPO:0002965
Synonyms:
Absence of delayed hypersensitivity skin test [HPO:0002965]
Lack of delayed skin hypersensitivity reaction [HPO:0002965]
Absence of delayed hypersensitivity skin test [OMIM:Absence of delayed hypersensitivity skin test]
Cutaneous anergy [OMIM:Cutaneous anergy]
Lack of delayed skin hypersensitivity reaction [OMIM:Lack of delayed skin hypersensitivity reaction]
Quality:
Cross references:
OMIM: "Absence of delayed hypersensitivity skin test" [OMIM:Absence of delayed hypersensitivity skin test]
OMIM: "Cutaneous anergy" [OMIM:Cutaneous anergy]
OMIM: "Lack of delayed skin hypersensitivity reaction" [OMIM:Lack of delayed skin hypersensitivity reaction]
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)
                            Cutaneous anergy(HPO:0002965)
       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)
                         Cutaneous anergy(HPO:0002965)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

CANDIDIASIS, FAMILIAL, 1 (OMIM:114580)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Immunodeficiency by defective expression of HLA class 2 (Orphanet:572)
MONOCYTE CHEMOTACTIC DISORDER (OMIM:252250)
SPLENOMEGALY SYNDROME WITH SPLENIC GERMINAL CENTER HYPOPLASIA ANDREDUCED CIRCULATING T HELPER CELLS (OMIM:183350)
T-B+ severe combined immunodeficiency due to JAK3 deficiency (Orphanet:35078)
Vici syndrome (Orphanet:1493)