Impaired T cell function
Symptom Information:
Symptom ID: | HPO:0005435 | |||||
Synonyms: |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) 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) Impaired T cell function(HPO:0005435) 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) Impaired T cell function(HPO:0005435) MedDRA: |
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Database Frequency: | 9 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
22q11.2 deletion syndrome | (Orphanet:567) |
Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIl | (OMIM:614576) |
Hereditary orotic aciduria | (Orphanet:30) |
IMMUNODEFICIENCY, COMMON VARIABLE, 1 | (OMIM:607594) |
IMMUNODEFICIENCY, COMMON VARIABLE, 2 | (OMIM:240500) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
T-CELL RECEPTOR-ALPHA/BETA DEFICIENCY | (OMIM:615387) |
VELOCARDIOFACIAL SYNDROME | (OMIM:192430) |