Immunodeficiency disease
MONDO:0021094Disease in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral.
Also known as: immuno-deficiency, immunodeficiency, immunodeficiency disorder, immunodeficiency syndrome
776 clinical trials for this condition and its sub-types, 55 tagged with Immunodeficiency disease itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Immunodeficiency disease
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T-cell immunodeficiency 4 trials · 484 incl. sub-types
3 sub-types
- AIDS 463 trials
- Congenital T-cell immunodeficiency 0 trials · 13 incl. sub-types Sub-types →
- Idiopathic CD4-positive T-lymphocytopenia 6 trials
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B cell deficiency 5 trials · 85 incl. sub-types
5 sub-types
- Agammaglobulinemia 16 trials · 52 incl. sub-types Sub-types →
- Hyperimmunoglobulin syndrome 0 trials · 33 incl. sub-types Sub-types →
- Selective immunoglobulin deficiency disease 1 trial · 4 incl. sub-types Sub-types →
- PAX5-related B lymphopenia and autism spectrum disorder 0 trials
- Immunoglobulin beta deficiency 0 trials
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Combined immunodeficiency 3 trials · 57 incl. sub-types
33 sub-types
- Severe combined immunodeficiency 24 trials · 37 incl. sub-types Sub-types →
- Ataxia telangiectasia 11 trials Sub-types →
- Wiskott-Aldrich syndrome 10 trials
- X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia 2 trials
- Combined immunodeficiency due to CRAC channel dysfunction 1 trial Sub-types →
- Combined immunodeficiency due to ZAP70 deficiency 1 trial
- Non-SCID combined immunodeficiency 0 trials · 1 incl. sub-types Sub-types →
- IRF4-related combined immunodeficiency 0 trials
- MHC class I deficiency 0 trials Sub-types →
- NFATC1-related combined immunodeficiency 0 trials
- POLD3-related combined immunodeficiency 0 trials
- RAC2-related combined immunodeficiency-bronchiectasis-cancer-predisposing syndrome 0 trials Sub-types →
- Autosomal dominant combined immunodeficiency due to ERBIN deficiency 0 trials
- Autosomal dominant combined immunodeficiency due to partial IL6ST deficiency 0 trials
- Autosomal recessive combined immunodeficiency due to IL6R deficiency 0 trials
- Autosomal recessive combined immunodeficiency due to complete IL6ST deficiency 0 trials
- Autosomal recessive combined immunodeficiency due to partial IL6ST deficiency 0 trials
- Combined immunodeficiency due to CD3gamma deficiency 0 trials
- Combined immunodeficiency due to CTPS1 deficiency 0 trials
- Combined immunodeficiency due to GINS1 deficiency 0 trials
- Combined immunodeficiency due to MALT1 deficiency 0 trials
- Combined immunodeficiency due to OX40 deficiency 0 trials
- Combined immunodeficiency due to POLE2 deficiency 0 trials
- Combined immunodeficiency due to RELA haploinsufficiency 0 trials
- Combined immunodeficiency due to STK4 deficiency 0 trials
- Combined immunodeficiency due to TBX1 deficiency 0 trials
- Combined immunodeficiency due to dimerization defective IKAROS mutation 0 trials
- Combined immunodeficiency due to moesin deficiency 0 trials
- Combined immunodeficiency syndrome 0 trials Sub-types →
- Combined immunodeficiency with low Ig due to BCL10 deficiency 0 trials
- Combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to IKBKA deficiency 0 trials
- Early-onset combined immunodeficiency with low ig due to dominant negative IKAROS mutation 0 trials
- Late-onset combined immunodeficiency due to ICOSL deficiency 0 trials
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Complement deficiency 2 trials · 28 incl. sub-types
8 sub-types
- Atypical hemolytic-uremic syndrome 19 trials Sub-types →
- Classic complement early component deficiency 0 trials · 7 incl. sub-types Sub-types →
- Disorder of lectin complement activation pathway 0 trials · 1 incl. sub-types Sub-types →
- Complement factor I deficiency 0 trials
- Complement receptor deficiency 0 trials
- Immunodeficiency due to a classical component pathway complement deficiency 0 trials Sub-types →
- Immunodeficiency due to a late component of complement deficiency 0 trials Sub-types →
- Recurrent Neisseria infections due to factor D deficiency 0 trials
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X-linked lymphoproliferative syndrome 7 trials · 11 incl. sub-types
2 sub-types
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GATA2 deficiency with susceptibility to MDS/AML 5 trials · 8 incl. sub-types
2 sub-types
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Idiopathic CD4 lymphocytopenia 7 trials
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IKBKG-related immunodeficiency with or without ectodermal dysplasia 0 trials · 4 incl. sub-types
3 sub-types
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IRF4-related immune disorder 1 trial
2 sub-types
- IRF4-related combined immunodeficiency 0 trials
- Immunodeficiency 131 0 trials
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Immunodeficiency 23 1 trial
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Immunodeficiency 31B 1 trial
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DOCK2 deficiency 0 trials
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FADD-related immunodeficiency 0 trials
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FASLG-related immunodeficiency 0 trials
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FNIP1-associated syndrome 0 trials
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Shwachman-Diamond syndrome 1 0 trials
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TNFRSF9-related immunodeficiency 0 trials
1 sub-type
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Wiskott-Aldrich syndrome 2 0 trials
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Hatipoglu immunodeficiency syndrome 0 trials
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Hypoproteinemia, hypercatabolic 0 trials
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Immunodeficiency 102 0 trials
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Immunodeficiency 112 0 trials
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Immunodeficiency 117 0 trials
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Immunodeficiency 118 0 trials
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Immunodeficiency 119 0 trials
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Immunodeficiency 122 0 trials
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Immunodeficiency 125 0 trials
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Immunodeficiency 127 0 trials
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Immunodeficiency 128 0 trials
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Immunodeficiency 132b 0 trials
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Immunodeficiency 15a 0 trials
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Immunodeficiency 35 0 trials
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Immunodeficiency 45 0 trials
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Immunodeficiency 53 0 trials
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Immunodeficiency 57 0 trials
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Immunodeficiency 60 0 trials
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Immunodeficiency 62 0 trials
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Immunodeficiency 64 0 trials
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Immunodeficiency 66 0 trials
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Immunodeficiency 67 0 trials
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Immunodeficiency 69 0 trials
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Immunodeficiency 70 0 trials
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Immunodeficiency 75 0 trials
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Immunodeficiency 76 0 trials
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Immunodeficiency 77 0 trials
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Immunodeficiency 81 0 trials
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Immunodeficiency 84 0 trials
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Immunodeficiency 85 and autoimmunity 0 trials
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Immunodeficiency 86 0 trials
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Immunodeficiency 87 and autoimmunity 0 trials
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Immunodeficiency 88 0 trials
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Immunodeficiency 89 and autoimmunity 0 trials
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Immunodeficiency 92 0 trials
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Immunodeficiency 95 0 trials
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Immunodeficiency 96 0 trials
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Lymphoproliferative syndrome 1 0 trials
Most studied deeper sub-types
Common variable immunodeficiency
(29)
Netherton syndrome
(15)
DiGeorge syndrome
(11)
T-B+ severe combined immunodeficiency due to gamma chain deficiency
(10)
Hyper-IgM syndrome
(8)
Syndromic agammaglobulinemia
(7)
Combined immunodeficiency due to DOCK8 deficiency
(6)
Immunodeficiency 14
(6)
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency
(6)
Activated PI3K-delta syndrome
(5)
C1 inhibitor deficiency
(5)
Hyper-IgE syndrome
(5)
Bruton-type agammaglobulinemia
(4)
Omenn syndrome
(4)
Hyper-IgE recurrent infection syndrome 1, autosomal dominant
(3)
Hyper-IgM syndrome type 1
(3)
Severe combined immunodeficiency due to DCLRE1C deficiency
(3)
Complement component 3 deficiency
(2)
Nezelof syndrome
(2)
Selective IgA deficiency disease
(2)