| D007153 |
Immunologic Deficiency Syndromes |
Syndromes in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral. |
Antibody Deficiency Syndrome,Deficiency Syndrome, Immunologic,Deficiency Syndromes, Antibody,Deficiency Syndromes, Immunologic,Immunologic Deficiency Syndrome,Immunological Deficiency Syndromes,Antibody Deficiency Syndromes,Deficiency Syndrome, Antibody,Deficiency Syndrome, Immunological,Deficiency Syndromes, Immunological,Immunological Deficiency Syndrome,Syndrome, Antibody Deficiency,Syndrome, Immunologic Deficiency,Syndrome, Immunological Deficiency,Syndromes, Antibody Deficiency,Syndromes, Immunologic Deficiency,Syndromes, Immunological Deficiency |
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| D008297 |
Male |
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Males |
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| D011951 |
Receptors, Complement |
Molecules on the surface of some B-lymphocytes and macrophages, that recognize and combine with the C3b, C3d, C1q, and C4b components of complement. |
Complement Receptors,Complement Receptor,Complement Receptor Type 1,Receptor, Complement |
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| D003165 |
Complement System Proteins |
Serum glycoproteins participating in the host defense mechanism of COMPLEMENT ACTIVATION that creates the COMPLEMENT MEMBRANE ATTACK COMPLEX. Included are glycoproteins in the various pathways of complement activation (CLASSICAL COMPLEMENT PATHWAY; ALTERNATIVE COMPLEMENT PATHWAY; and LECTIN COMPLEMENT PATHWAY). |
Complement Proteins,Complement,Complement Protein,Hemolytic Complement,Complement, Hemolytic,Protein, Complement,Proteins, Complement,Proteins, Complement System |
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| D005260 |
Female |
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Females |
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| D006801 |
Humans |
Members of the species Homo sapiens. |
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man |
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| D017098 |
IgA Deficiency |
A dysgammaglobulinemia characterized by a deficiency of IMMUNOGLOBULIN A. |
Deficiency, IgA,Deficiencies, IgA,IgA Deficiencies |
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| D017099 |
IgG Deficiency |
A dysgammaglobulinemia characterized by a deficiency of IMMUNOGLOBULIN G. |
Deficiency, IgG,Deficiencies, IgG,IgG Deficiencies |
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