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