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:
Lymphoid and complement immunodeficiency
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Lymphoid
and
complement
disorders causing
immunodeficiency
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
HIV/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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