T lymphocytopenia
Symptom Information:
Symptom ID: | HPO:0005403 | |||||||
Synonyms: |
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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 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 number(HPO:0011839) T lymphocytopenia(HPO:0005403) 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 number(HPO:0011839) T lymphocytopenia(HPO:0005403) MedDRA: |
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Database Frequency: | 10 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
ATAXIA-TELANGIECTASIA | (OMIM:208900) |
Combined immunodeficiency with skin granulomas | (Orphanet:157949) |
ICF syndrome | (Orphanet:2268) |
IMMUNODEFICIENCY 25 | (OMIM:610163) |
IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTSAND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES | (OMIM:242870) |
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME1 | (OMIM:242860) |
Immunodeficiency due to CD25 deficiency | (Orphanet:169100) |
Nijmegen breakage syndrome | (Orphanet:647) |
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION | (OMIM:607944) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |