Abnormality of T cells
Symptom Information:
Symptom ID: | HPO:0002843 | |||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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 blood and blood-forming tissues(HPO:0001871) Abnormality of leukocytes(HPO:0001881) Abnormality of lymphocytes(HPO:0004332) Abnormality of T cells(HPO:0002843) MedDRA: |
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Database Frequency: | 7 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
Autoimmune polyendocrinopathy type 2 | (Orphanet:3143) |
CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME | (OMIM:215250) |
LYMPHOID SYSTEM DETERIORATION, PROGRESSIVE | (OMIM:247630) |
OKT4 EPITOPE DEFICIENCY | (OMIM:613949) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Thymic aplasia | (Orphanet:83471) |