Reduced delayed hypersensitivity
Symptom Information:
Symptom ID: | HPO:0002972 | |||||||
Synonyms: |
|
|||||||
Quality: | ||||||||
Cross references: |
|
|||||||
Is a (Direct Parents): |
|
|||||||
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) |