Pages that link to "Complement 3 deficiency"
Showing 50 items.
- Severe combined immunodeficiency (links | edit)
- Hypersensitivity (links | edit)
- Paroxysmal nocturnal hemoglobinuria (links | edit)
- Immunodeficiency (links | edit)
- Adenosine deaminase deficiency (links | edit)
- Hereditary angioedema (links | edit)
- Angioedema (links | edit)
- Leukopenia (links | edit)
- Ataxia–telangiectasia (links | edit)
- Immunodeficiency–centromeric instability–facial anomalies syndrome (links | edit)
- Wiskott–Aldrich syndrome (links | edit)
- Omenn syndrome (links | edit)
- X-linked agammaglobulinemia (links | edit)
- Hypogammaglobulinemia (links | edit)
- Common variable immunodeficiency (links | edit)
- Lymphocytopenia (links | edit)
- ZAP70 deficiency (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Antibody-dependent cellular cytotoxicity (links | edit)
- Hyperimmunoglobulin E syndrome (links | edit)
- X-linked severe combined immunodeficiency (links | edit)
- Selective immunoglobulin A deficiency (links | edit)
- HIV/AIDS (links | edit)
- Idiopathic CD4+ lymphocytopenia (links | edit)
- Combined immunodeficiencies (links | edit)
- Nezelof syndrome (links | edit)
- Dysgammaglobulinemia (links | edit)
- Bare lymphocyte syndrome (links | edit)
- Hyper IgM syndrome (links | edit)
- Hyper-IgM syndrome type 1 (links | edit)
- Hyper-IgM syndrome type 2 (links | edit)
- Hyper-IgM syndrome type 5 (links | edit)
- Primary immunodeficiency (links | edit)
- Properdin deficiency (links | edit)
- Purine nucleoside phosphorylase deficiency (links | edit)
- Complement deficiency (links | edit)
- WHIM syndrome (links | edit)
- Immune disorder (links | edit)
- IgG deficiency (links | edit)
- Transient hypogammaglobulinemia of infancy (links | edit)
- Outline of immunology (links | edit)
- Isolated primary immunoglobulin M deficiency (links | edit)
- Humoral immune deficiency (links | edit)
- Complement 2 deficiency (links | edit)
- Hyper-IgM syndrome type 3 (links | edit)
- Hyper-IgM syndrome type 4 (links | edit)
- Acquired C1 esterase inhibitor deficiency (links | edit)
- Thymic hypoplasia (links | edit)
- Complement 4 deficiency (links | edit)
- Terminal complement pathway deficiency (links | edit)