Rubinstein-Taybi syndrome

rare disease
MedicalCondition designated_intractable_rare_disease Q666980
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Summary

Rubinstein-Taybi syndrome is a designated intractable/rare disease[1]. It draws 306 Wikipedia views per month (designated_intractable_rare_disease category, ranking #74 of 201).[2]

Key Facts

  • Rubinstein-Taybi syndrome's instance of is recorded as designated intractable/rare disease[3].
  • Rubinstein-Taybi syndrome's instance of is recorded as rare disease[4].
  • Rubinstein-Taybi syndrome's instance of is recorded as class of disease[5].
  • Hooshang Taybi is named after Rubinstein-Taybi syndrome[6].
  • Jack Rubinstein is named after Rubinstein-Taybi syndrome[7].
  • Rubinstein-Taybi syndrome is a type of autosomal dominant disease[8].
  • Rubinstein-Taybi syndrome is a type of syndrome[9].
  • Rubinstein-Taybi syndrome is a type of chromosomal deletion syndrome[10].
  • Rubinstein-Taybi syndrome is a type of disease[11].
  • Rubinstein-Taybi syndrome's Commons category is recorded as Rubinstein-Taybi syndrome[12].
  • Rubinstein-Taybi syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4067[13].
  • Rubinstein-Taybi syndrome's ICD-9-CM is recorded as 759.89[14].
  • Rubinstein-Taybi syndrome's NCI Thesaurus ID is recorded as C75466[15].
  • Rubinstein-Taybi syndrome's health specialty is recorded as medical genetics[16].
  • Rubinstein-Taybi syndrome's genetic association is recorded as EP300[17].
  • Rubinstein-Taybi syndrome's genetic association is recorded as CREBBP[18].
  • Rubinstein-Taybi syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_1933[19].
  • Rubinstein-Taybi syndrome's exact match is recorded as http://identifiers.org/doid/DOID:1933[20].
  • Rubinstein-Taybi syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_783[21].
  • Rubinstein-Taybi syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[22].

Why It Matters

Rubinstein-Taybi syndrome draws 306 Wikipedia views per month (designated_intractable_rare_disease category, ranking #74 of 201).[2] It has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[23] It is known by 6 alternative names across languages and contexts.[24]

References

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

Direct Wikidata claims

  1. [3] ↑ . nanbyou.or.jp. Retrieved . nanbyou.or.jp. Provenance: wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [9] ↑ . Disease Ontology. Retrieved . wikidata.org.
  8. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  12. [14] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  13. [15] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . Genetic heterogeneity in Rubinstein-Taybi syndrome: mutations in both the CBP and EP300 genes cause disease. wikidata.org.
  16. [18] ↑ . Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  17. [19] ↑ . Disease Ontology. Retrieved . wikidata.org.
  18. [20] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [23] ↑ . Wikidata sitelinks. wikidata.org.
  3. [24] ↑ . 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). Rubinstein-Taybi syndrome. Retrieved October 13, 2026, from https://4ort.xyz/entity/rubinstein-taybi-syndrome
MLA “Rubinstein-Taybi syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 13 Oct. 2026, https://4ort.xyz/entity/rubinstein-taybi-syndrome.
BibTeX @misc{4ortxyz_rubinstein-taybi-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Rubinstein-Taybi syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/rubinstein-taybi-syndrome}, note = {Accessed: 2026-10-13}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Rubinstein-Taybi syndrome — https://4ort.xyz/entity/rubinstein-taybi-syndrome (retrieved 2026-10-13)

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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. 14w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of → autosomal dominant disease, syndrome, chromosomal deletion syndrome +1
    Named after → —
    Health specialty → medical genetics
    Genetic association → EP300, CREBBP
    + 6 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39732|batch #39732]]: rm redundant subclass"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.