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
  1. B cell deficiency MONDO:0002211 80
  2. Complement deficiency MONDO:0003832 37
  3. Lymphoproliferative syndrome MONDO:0016537 23
  4. Chronic mucocutaneous candidiasis MONDO:0015279 12
  5. Aicardi-Goutieres syndrome MONDO:0018866 11
  6. Hereditary hemophagocytic lymphohistiocytosis MONDO:0015541 11
  7. Phagocyte bactericidal dysfunction MONDO:0005910 8
  8. Immuno-osseous dysplasia MONDO:0015708 5
  9. IL10-related early-onset inflammatory bowel disease MONDO:0016542 2
  10. Ectodermal dysplasia and immune deficiency MONDO:0010293 2
  11. Trichohepatoenteric syndrome MONDO:0009105 2
  12. Immunodeficiency 37 MONDO:0014491 BCL10 1
  13. Immunoglobulin heavy chain deficiency MONDO:0015697 1
  14. A20 haploinsufficiency MONDO:0100222 TNFAIP3
  15. BENTA disease MONDO:0014645 CARD11
  16. NK cell deficiency MONDO:0850199
  17. STAT5 haploinsufficiency MONDO:1060224
  18. Say-Barber-Miller syndrome MONDO:0009620
  19. T cell and NK cell immunodeficiency MONDO:0850200
  20. T-cell immunodeficiency with epidermodysplasia verruciformis MONDO:0017925
  21. X-linked immunoneurologic disorder MONDO:0010243
  22. Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity MONDO:0014313 FCGR3A
  23. Combined immunodeficiency due to moesin deficiency MONDO:0010514 MSN
  24. Combined immunodeficiency with faciooculoskeletal anomalies MONDO:0013226
  25. Dendritic cell deficiency MONDO:0850812
  26. Familial isolated congenital asplenia MONDO:0010066 RPSA
  27. Hepatic veno-occlusive disease-immunodeficiency syndrome MONDO:0009338 SP110
  28. Immune dysregulation with immunodeficiency due to AIOLOS haploinsufficiency MONDO:0979328 IKZF3
  29. Immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome MONDO:0033968
  30. Immunodeficiency 28 MONDO:0013953 IFNGR2
  31. Immunodeficiency 33 MONDO:0010386
  32. Immunodeficiency 39 MONDO:0014597 IRF7
  33. Immunodeficiency 47 MONDO:0010504 ATP6AP1
  34. Immunodeficiency 49 MONDO:0014981 BCL11B
  35. Immunodeficiency with defective T-cell response to interleukin 1 MONDO:0009464
  36. Immunodeficiency, X-linked, with deficiency of 115,000 Dalton surface glycoprotein MONDO:0010625
  37. Immunodysregulation with variable immunodeficiency and autoimmunity MONDO:0979233 IKZF2
  38. Inflammatory bowel disease-recurrent sinopulmonary infections syndrome MONDO:0033969
  39. Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection MONDO:0014715 STAT2
  40. Properdin deficiency, X-linked MONDO:0010713 CFP
  41. Recurrent infections associated with rare immunoglobulin isotypes deficiency MONDO:0013576 IGKC

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