Impaired Ig class switch recombination
Symptom Information:
Symptom ID: | HPO:0002959 | ||||
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 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 physiology(HPO:0005372) Impaired Ig class switch recombination(HPO:0002959) 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 physiology(HPO:0005372) Impaired Ig class switch recombination(HPO:0002959) MedDRA: |
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Database Frequency: | 5 / 7739 | ||||
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All diseases associated with this symptom:
Hyper-IgM syndrome type 2 | (Orphanet:101089) |
Hyper-IgM syndrome type 3 | (Orphanet:101090) |
Hyper-IgM syndrome type 4 | (Orphanet:101091) |
Hyper-IgM syndrome type 5 | (Orphanet:101092) |
X-linked hyper-IgM syndrome | (Orphanet:101088) |