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| Term | combined T cell and B cell immunodeficiency | ID (Ontology) | DOID:628 (Human Disease) |
| Definition | A primary immunodeficiency disease characterized by impaired T cell-mediated immunity and impaired B cell mediated humoral immunity. | ||
| Also Known As | "Congenital Combined Immunodeficiency" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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primary immunodeficiency disease |__combined immunodeficiency |__combined T cell and B cell immunodeficiency 30 rec. |__CD40 ligand deficiency |__DNA ligase IV deficiency 1 rec. |__Good syndrome |__immunodeficiency 14 1 rec. |__immunodeficiency 15A 1 rec. |__immunodeficiency 16 |__immunodeficiency 23 1 rec. |__immunodeficiency 36 1 rec. |__immunodeficiency 37 |__immunodeficiency 40 1 rec. |__immunodeficiency 46 |__immunodeficiency 53 1 rec. |__immunodeficiency 56 |__immunodeficiency 58 1 rec. |__immunodeficiency 60 |__immunodeficiency 70 6 rec. |__immunodeficiency 98 8 rec. |__immunodeficiency 99 1 rec. |__immunodeficiency 120 1 rec. |__leukocyte adhesion deficiency 3 rec. | |__leukocyte adhesion deficiency 1 1 rec. | |__leukocyte adhesion deficiency 2 | |__leukocyte adhesion deficiency 3 2 rec. |__purine nucleoside phosphorylase deficiency 2 rec. |__X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia 1 rec. |
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| Is a | combined immunodeficiency | ||
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ICD10CM:D81 ICD9CM:279.2 NCI:C27871 ORDO:101972 SNOMEDCT_US_2023_03_01:442459007 UMLS_CUI:C2711630 |
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