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Template:Lymphoid and complement immunodeficiency

From WikiMD's medical encyclopedia

Immune disorders: Lymphoid and complement immunodeficiency (D80–D85, 279.0–4)
Primary
Antibody/humoral
(B)
Hypogammaglobulinemia
* X-linked agammaglobulinemia
  • Transient hypogammaglobulinemia of infancy
Dysgammaglobulinemia
* IgA deficiency
  • IgG deficiency
  • IgM deficiency
  • Hyper IgM syndrome (1
  • 2
  • 3
  • 4
  • 5)
  • Wiskott–Aldrich syndrome
  • Hyper-IgE syndrome
Other
* Common variable immunodeficiency
  • ICF syndrome
T cell deficiency
(T)
* thymic hypoplasia: hypoparathyroid (Di George's syndrome)
  • euparathyroid (Nezelof syndrome
  • Ataxia–telangiectasia)

peripheral: Purine nucleoside phosphorylase deficiency

  • Hyper IgM syndrome (1)
Severe combined
(B+T)
* x-linked: X-SCID
autosomal: Adenosine deaminase deficiency
  • Omenn syndrome
  • ZAP70 deficiency
  • Bare lymphocyte syndrome
Acquired
* AIDS
Leukopenia:
Lymphocytopenia
* Idiopathic CD4+ lymphocytopenia
Complement
deficiency
* C1-inhibitor (Angioedema/Hereditary angioedema)
  • Complement 2 deficiency/Complement 4 deficiency
  • MBL deficiency
  • Properdin deficiency
  • Complement 3 deficiency
  • Terminal complement pathway deficiency
  • Paroxysmal nocturnal hemoglobinuria
  • Complement receptor deficiency


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  • This page was last edited on 8 March 2025, at 19:32.
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