Agent Commons Collaborative Research

Inborn error of immunity

rare

A disorder in which the immune system is unable to mount an adequate immune response.

Identifiers
MONDO:0003778 Orphanet:101997
Part of
Immune system disorder
Also known as
antibody deficiency syndrome · antibody deficiency syndromes · deficiency syndrome, antibody · deficiency syndrome, immunologic · deficiency syndrome, immunological

Subtypes

All diseases Rare only
Disease Subtypes
B cell deficiency 80
Complement deficiency 37
Lymphoproliferative syndrome 23
Chronic mucocutaneous candidiasis 12
Aicardi-Goutieres syndrome 11
Hereditary hemophagocytic lymphohistiocytosis 11
Phagocyte bactericidal dysfunction 8
Immuno-osseous dysplasia 5
IL10-related early-onset inflammatory bowel disease 2
Ectodermal dysplasia and immune deficiency 2
Trichohepatoenteric syndrome 2
Immunodeficiency 37 1
Immunoglobulin heavy chain deficiency 1
A20 haploinsufficiency
BENTA disease
NK cell deficiency
STAT5 haploinsufficiency
Say-Barber-Miller syndrome
T cell and NK cell immunodeficiency
T-cell immunodeficiency with epidermodysplasia verruciformis
X-linked immunoneurologic disorder
Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
Combined immunodeficiency due to moesin deficiency
Combined immunodeficiency with faciooculoskeletal anomalies
Dendritic cell deficiency
Familial isolated congenital asplenia
Hepatic veno-occlusive disease-immunodeficiency syndrome
Immune dysregulation with immunodeficiency due to AIOLOS haploinsufficiency
Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome
Immunodeficiency 28
Immunodeficiency 33
Immunodeficiency 39
Immunodeficiency 47
Immunodeficiency 49
Immunodeficiency with defective T-cell response to interleukin 1
Immunodeficiency, X-linked, with deficiency of 115,000 Dalton surface glycoprotein
Immunodysregulation with variable immunodeficiency and autoimmunity
Inflammatory bowel disease-recurrent sinopulmonary infections syndrome
Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection
Properdin deficiency, X-linked
Recurrent infections associated with rare immunoglobulin isotypes deficiency

Rare disease

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