common variable immunodeficiency

immune disorder
MedicalCondition rare_disease Q1472818
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common variable immunodeficiency

Summary

common variable immunodeficiency is a rare disease[1]. It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • common variable immunodeficiency's instance of is recorded as rare disease[3].
  • common variable immunodeficiency's instance of is recorded as health problem[4].
  • common variable immunodeficiency's instance of is recorded as class of disease[5].
  • common variable immunodeficiency is a type of agammaglobulinemia[6].
  • common variable immunodeficiency is a type of autoimmune disease[7].
  • common variable immunodeficiency is a type of disease[8].
  • common variable immunodeficiency's symptoms and signs is recorded as agammaglobulinemia[9].
  • common variable immunodeficiency's symptoms and signs is recorded as opportunistic infection[10].
  • common variable immunodeficiency's symptoms and signs is recorded as fatigue[11].
  • common variable immunodeficiency's symptoms and signs is recorded as malignancy[12].
  • common variable immunodeficiency's symptoms and signs is recorded as Nodular regenerative hyperplasia[13].
  • common variable immunodeficiency's possible treatment is recorded as symptomatic treatment[14].
  • common variable immunodeficiency's ICD-9-CM is recorded as 279.06[15].
  • common variable immunodeficiency's NCI Thesaurus ID is recorded as C26725[16].
  • common variable immunodeficiency's health specialty is recorded as immunology[17].
  • common variable immunodeficiency's genetic association is recorded as TNFRSF13B[18].
  • common variable immunodeficiency's genetic association is recorded as CR2[19].
  • common variable immunodeficiency's genetic association is recorded as IL21[20].
  • common variable immunodeficiency's genetic association is recorded as TNFRSF13C[21].
  • common variable immunodeficiency's genetic association is recorded as CD81[22].
  • common variable immunodeficiency's genetic association is recorded as NFKB2[23].
  • common variable immunodeficiency's genetic association is recorded as CD19[24].
  • common variable immunodeficiency's genetic association is recorded as ICOS[25].
  • common variable immunodeficiency's genetic association is recorded as LRBA[26].
  • common variable immunodeficiency's genetic association is recorded as MS4A1[27].

Why It Matters

common variable immunodeficiency has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2] It is known by 16 alternative names across languages and contexts.[28]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . Disease Ontology. Retrieved . wikidata.org.
  5. [7] . Disease Ontology. Retrieved . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Disease Ontology. Retrieved . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . Mutations in TNFRSF13B encoding TACI are associated with common variable immunodeficiency in humans.. wikidata.org.
  17. [19] . Genetic CD21 deficiency is associated with hypogammaglobulinemia. wikidata.org.
  18. [20] . Early-onset inflammatory bowel disease and common variable immunodeficiency-like disease caused by IL-21 deficiency. wikidata.org.
  19. [21] . B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans.. wikidata.org.
  20. [22] . CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency. wikidata.org.
  21. [23] . Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency. wikidata.org.
  22. [24] . An antibody-deficiency syndrome due to mutations in the CD19 gene. wikidata.org.
  23. [25] . Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency. wikidata.org.
  24. [26] . Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity. wikidata.org.
  25. [27] . CD20 deficiency in humans results in impaired T cell-independent antibody responses. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [28] . Wikidata aliases. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). common variable immunodeficiency. Retrieved May 3, 2026, from https://4ort.xyz/entity/common-variable-immunodeficiency
MLA “common variable immunodeficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/common-variable-immunodeficiency.
BibTeX @misc{4ortxyz_common-variable-immunodeficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{common variable immunodeficiency}}, year = {2026}, url = {https://4ort.xyz/entity/common-variable-immunodeficiency}, note = {Accessed: 2026-05-03}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 2d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of agammaglobulinemia, autoimmune disease, disease
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39732|batch #39732]]: rm redundant subclass"
  2. 29d ago · Comfyquiettree · 2026-06-06 view diff on Wikidata ↗
    Subclass of
    On focus list of wikimedia project WikiProject Medicine
    Subclass of agammaglobulinemia, autoimmune disease, disease
    Has phenotype agammaglobulinemia
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-create:1||1 */ [[Property:P3471]]: 4127, Matched to [[:toollabs:mix-n-match/#/entry/78311198|Běžná variabilní imunodeficience (#78311198)]] in [[:toollabs:mix-n-match/#/catalog/2686|Wiki"
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