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Icf Syndrome
ICF syndrome
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Immunodeficiency
(13)
Adenosine deaminase deficiency
Bare lymphocyte syndrome
Common variable immunodeficiency
Nezelof syndrome
X-scid
X-scid
Complement deficiency
HIV
HIV/AIDS
Idiopathic CD4+ lymphocytopenia
Immunodeficiency (Acquired immunodeficiency)
Primary immunodeficiency
Severe combined immunodeficiency
Severe combined immunodeficiency (non-human)
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Autosomal recessive disorders
Zap70 deficiency
Mevalonic aciduria
Purine nucleoside phosphorylase deficiency
Omenn syndrome
Nezelof syndrome
Adenosine deaminase deficiency
Bare lymphocyte syndrome
Genetic disorder
Myeloperoxidase deficiency
Zap70 deficiency
Adenosine deaminase deficiency
Purine nucleoside phosphorylase deficiency
Genetic disorders
(16)
WHIM syndrome
22q11.2 deletion syndrome
Hyper IgM syndrome
Ataxia telangiectasia
Wiskott-aldrich syndrome
Wiskott-aldrich syndrome
Adrenoleuk- odystrophy
Chronic granulomatous disease
Zap70 deficiency
Nezelof syndrome
Adenosine deaminase deficiency
Myeloperoxidase deficiency
Mevalonic aciduria
Purine nucleoside phosphorylase deficiency
Omenn syndrome
X-scid
Bare lymphocyte syndrome
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Rare diseases
Zap70 deficiency
WHIM syndrome
Adenosine deaminase deficiency
Purine nucleoside phosphorylase deficiency
Omenn syndrome
Wiskott-aldrich syndrome
Immune system
Immune disorders
Lymphoid
Antibody
Cell-mediated
Hyper IgM syndrome
Myeloperoxidase deficiency
Syndromes
Nezelof syndrome
WHIM syndrome
22q11.2 deletion syndrome
Omenn syndrome
Immunology
Hyper IgM syndrome
Myeloperoxidase deficiency
Cell-mediated
Blood disorders
Hematological malignancy
Hematology
Monoclonal gammopathy of undetermined significance
Wiskott-aldrich syndrome
Lymphatic system
Lymphatic disease
Marginal zone
Myeloid
Noninfectious immunodeficiency-related cutaneous conditions
(26)
IgM deficiency
22q11.2 deletion syndrome
Bare lymphocyte syndrome
Cartilage–hair hypoplasia
Chediak–Higashi syndrome
Chediak–Higashi syndrome
Chronic granulomatous disease
Common variable immunodeficiency
Complement deficiency
Graft-versus-host disease
Griscelli syndrome
Hyperimmunoglobulin E syndrome
Immunodeficiency with hyper-immu- noglobulin M
Leukocyte adhesion molecule deficiency
Myeloperoxidase deficiency
Neutropenia
Nezelof syndrome
Omenn syndrome
Purine nucleoside phosphorylase deficiency
Selective immunoglobulin A deficiency
Severe combined immunodeficiency
Thymoma with immunodeficiency
WHIM syndrome
Wiskott-aldrich syndrome
X-linked agammaglobulinemia
X-linked hyper-immu- noglobulin M syndrome
X-linked lymphoproliferative disease
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Diseases and disorders
(21)
Complement 2 deficiency
Heavy chain disease
Immunoproliferative
Angioedema
Hypogammag- lobulinemia
Hypogammag- lobulinemia
Zap70 deficiency
Nezelof syndrome
Adenosine deaminase deficiency
22q11.2 deletion syndrome
Hyper IgM syndrome
IgM deficiency
Myeloperoxidase deficiency
Mevalonic aciduria
Purine nucleoside phosphorylase deficiency
Omenn syndrome
Ataxia telangiectasia
Bare lymphocyte syndrome
Monoclonal gammopathy of undetermined significance
Common variable immunodeficiency
Wiskott-aldrich syndrome
Chronic granulomatous disease
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See also
(8)
Histology
Autoimmune disease
Dnmt3b
Lupus pernio
DNA methyltransferase
DNA methyltransferase
Cytosol
Methylation
Mutations
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