Agent Commons Collaborative Research

Immunodeficiency disease

Disease in which there is a deficiency or defect in the mechanisms of immunity, either cellular or humoral.

Identifiers
MONDO:0021094
Part of
Hereditary diseaseImmune system disorder
Also known as
immuno-deficiency · immunodeficiency · immunodeficiency disorder · immunodeficiency syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Combined immunodeficiency 101
B cell deficiency 80
Complement deficiency 37
T-cell immunodeficiency 5
IKBKG-related immunodeficiency with or without ectodermal dysplasia 3
GATA2 deficiency with susceptibility to MDS/AML 2
X-linked lymphoproliferative syndrome 2
IRF4-related immune disorder 1
TNFRSF9-related immunodeficiency 1
Immunodeficiency 37 1
DNAJC21-related Shwachman Diamond syndrome
DOCK2 deficiency
FADD-related immunodeficiency
FNIP1-associated syndrome
Pelger-Huet-like anomaly and episodic fever with abdominal pain
Shwachman-Diamond syndrome 1
TFRC-related combined immunodeficiency
Wiskott-Aldrich syndrome 2
Wiskott-Aldrich syndrome, autosomal dominant form
Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome
Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
Cryptosporidiosis-chronic cholangitis-liver disease syndrome
Hypoproteinemia, hypercatabolic
Idiopathic CD4 lymphocytopenia
Immune deficiency due to impaired neutrophil phagocytosis and migration
Immunodeficiency 102
Immunodeficiency 114, folate-responsive
Immunodeficiency 117
Immunodeficiency 15a
Immunodeficiency 23
Immunodeficiency 28
Immunodeficiency 31B
Immunodeficiency 32B
Immunodeficiency 35
Immunodeficiency 39
Immunodeficiency 47
Immunodeficiency 51
Immunodeficiency 53
Immunodeficiency 62
Immunodeficiency 64
Immunodeficiency 67
Immunodeficiency 69
Immunodeficiency 75
Immunodeficiency 76
Immunodeficiency 82 with systemic inflammation
Immunodeficiency 84
Immunodeficiency 92
Immunodeficiency 98 with autoinflammation, X-linked
Immunodeficiency due to CD25 deficiency
Immunodeficiency due to selective anti-polysaccharide antibody deficiency
Lymphoproliferative syndrome 1
Myalgic encephalomeyelitis/chronic fatigue syndrome
Platelet abnormalities with eosinophilia and immune-mediated inflammatory disease
Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency
Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection
Pulmonary alveolar proteinosis with hypogammaglobulinemia
Pyogenic bacterial infections due to MyD88 deficiency

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