B lymphocytopenia
Symptom Information:
Symptom ID: | HPO:0010976 | ||||
Synonyms: |
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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 B cells(HPO:0002846) Abnormality of B cell number(HPO:0010975) B lymphocytopenia(HPO:0010976) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormality of leukocytes(HPO:0001881) Abnormality of lymphocytes(HPO:0004332) Abnormality of B cells(HPO:0002846) Abnormality of B cell number(HPO:0010975) B lymphocytopenia(HPO:0010976) MedDRA: |
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Database Frequency: | 8 / 7739 | ||||
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All diseases associated with this symptom:
Autosomal agammaglobulinemia | (Orphanet:33110) |
Combined immunodeficiency with skin granulomas | (Orphanet:157949) |
IMMUNODEFICIENCY, COMMON VARIABLE, 1 | (OMIM:607594) |
NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT | (OMIM:613107) |
Nijmegen breakage syndrome | (Orphanet:647) |
Omenn syndrome | (Orphanet:39041) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
Severe combined immunodeficiency due to complete RAG1/2 deficiency | (Orphanet:331206) |