BENTA disease

human disease

Facts

8 properties
Instance of
rare disease, class of disease[2]
Subclass of
combined immunodeficiency, non-severe combined immunodeficiency[3][4]
Age of onset
infantile onset[8]
Genetic association
CARD11[7]
Health specialty
immunology[6]
P14914
D464336[13]
Prevalence
+0.000001[5]
🏷️ Also known as
en B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY en B-CELL EXPANSION WITH NFKB AND T-CELL ANERGY; BENTA en B-cell expansion with NF-kB and T-cell anergy disease en BENTA en BENTA disease fr maladie BENTA ja ベンタ病
🔖 Identifiers · 9
Exact match
www.orpha.net
GARD rare disease ID
13339
Microsoft Academic ID (discontinued)
2780211837
OMIM ID
616452
Orphanet ID
464336
UMLS CUI
CN231446
UniProt disease ID
DI-04476
WikiProjectMed ID
BENTA disease

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Summary

BENTA disease is a rare disease[1].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [5] ↑ . Retrieved . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . Oncogenic CARD11 mutations in human diffuse large B cell lymphoma. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  7. [8] ↑ . Retrieved . wikidata.org.
  8. [9] ↑ . Retrieved . wikidata.org.
  9. [10] ↑ . Retrieved . wikidata.org.
  10. [11] ↑ . Retrieved . wikidata.org.
  11. [12] ↑ . Retrieved . wikidata.org.
  12. [13] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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). BENTA disease. Retrieved November 5, 2026, from https://4ort.xyz/entity/benta-disease
MLA “BENTA disease.” 4ort.xyz Knowledge Graph, 4ort.xyz, 5 Nov. 2026, https://4ort.xyz/entity/benta-disease.
BibTeX @misc{4ortxyz_benta-disease_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{BENTA disease}}, year = {2026}, url = {https://4ort.xyz/entity/benta-disease}, note = {Accessed: 2026-11-05}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): BENTA disease — https://4ort.xyz/entity/benta-disease (retrieved 2026-11-05)

Canonical URL: https://4ort.xyz/entity/benta-disease · Last refreshed:

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. 16d ago · ACorrêa (WMB) · 2026-10-24 view diff on Wikidata ↗
    Sitelink count → 1
    Prevalence → {'amount': '+0.000001'}
    Wikipedia languages → ['en']
    Age of onset → infantile onset
    + 3 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||pt, pt-br */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61469|batch #61469]]: Raras.org data import"
  2. 18w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Mondo ID → MONDO_0014645
    Imported from → —
    WikiProjectMed ID → BENTA disease
    UMLS CUI → CN231446
    + 11 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39953|batch #39953]]: deprecate redundant disease superclasses (2)"
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