Bannayan-Riley-Ruvalcaba syndrome

a rare overgrowth syndrome and hamartomatous disorder with occurrence of multiple subcutaneous lipomas, macrocephaly and hemangiomas.
MedicalCondition developmental_defect_during_embryogenesis Q474254
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Bannayan-Riley-Ruvalcaba syndrome

Summary

Bannayan-Riley-Ruvalcaba syndrome is a developmental defect during embryogenesis[1]. It draws 22 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #124 of 308).[2]

Key Facts

  • Bannayan-Riley-Ruvalcaba syndrome's instance of is recorded as developmental defect during embryogenesis[3].
  • Bannayan-Riley-Ruvalcaba syndrome's instance of is recorded as rare disease[4].
  • Bannayan-Riley-Ruvalcaba syndrome's instance of is recorded as class of disease[5].
  • Bannayan-Riley-Ruvalcaba syndrome is a type of autosomal dominant disease[6].
  • Bannayan-Riley-Ruvalcaba syndrome is a type of multiple hamartoma syndrome[7].
  • Bannayan-Riley-Ruvalcaba syndrome is a type of inherited digestive tract tumor[8].
  • Bannayan-Riley-Ruvalcaba syndrome is a type of rare genetic vascular tumor[9].
  • Bannayan-Riley-Ruvalcaba syndrome is a type of brain cancer[10].
  • Bannayan-Riley-Ruvalcaba syndrome is a type of complex vascular malformation with associated anomalies[11].
  • Bannayan-Riley-Ruvalcaba syndrome is a type of rare nervous system tumor[12].
  • Bannayan-Riley-Ruvalcaba syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[13].
  • Bannayan-Riley-Ruvalcaba syndrome is a type of genetic syndromic intellectual disability[14].
  • Bannayan-Riley-Ruvalcaba syndrome is a type of genetic skin vascular disorder[15].
  • Bannayan-Riley-Ruvalcaba syndrome is a type of overgrowth syndrome[16].
  • Bannayan-Riley-Ruvalcaba syndrome is a type of penile disease[17].
  • Bannayan-Riley-Ruvalcaba syndrome is a type of syndrome[18].
  • Bannayan-Riley-Ruvalcaba syndrome's ICD-9-CM is recorded as 759.6[19].
  • Bannayan-Riley-Ruvalcaba syndrome's NCI Thesaurus ID is recorded as C3939[20].
  • Bannayan-Riley-Ruvalcaba syndrome's health specialty is recorded as oncology[21].
  • Bannayan-Riley-Ruvalcaba syndrome's health specialty is recorded as medical genetics[22].
  • Bannayan-Riley-Ruvalcaba syndrome's genetic association is recorded as PTEN[23].
  • Bannayan-Riley-Ruvalcaba syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050657[24].
  • Bannayan-Riley-Ruvalcaba syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050657[25].
  • Bannayan-Riley-Ruvalcaba syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_109[26].
  • Bannayan-Riley-Ruvalcaba syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[27].

Why It Matters

Bannayan-Riley-Ruvalcaba syndrome draws 22 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #124 of 308).[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[28] It is known by 27 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . Disease Ontology. Retrieved . wikidata.org.
  5. [7] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [10] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [11] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  10. [12] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  11. [13] . Monarch Disease Ontology release 2018-06-29. Retrieved . 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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  15. [17] . Disease Ontology. Retrieved . wikidata.org.
  16. [18] . Disease Ontology. Retrieved . wikidata.org.
  17. [19] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  18. [20] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . Germline mutations in PTEN are present in Bannayan-Zonana syndrome. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  22. [24] . Disease Ontology. Retrieved . wikidata.org.
  23. [25] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  24. [26] . wikidata.org.
  25. [27] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . 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). Bannayan-Riley-Ruvalcaba syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/bannayan-riley-ruvalcaba-syndrome
MLA “Bannayan-Riley-Ruvalcaba syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/bannayan-riley-ruvalcaba-syndrome.
BibTeX @misc{4ortxyz_bannayan-riley-ruvalcaba-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Bannayan-Riley-Ruvalcaba syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/bannayan-riley-ruvalcaba-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Bannayan-Riley-Ruvalcaba syndrome — https://4ort.xyz/entity/bannayan-riley-ruvalcaba-syndrome (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/bannayan-riley-ruvalcaba-syndrome · 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. 7w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Health specialty oncology, medical genetics
    Genetic association PTEN
    Subclass of
    Instance of developmental defect during embryogenesis, rare disease, class of disease
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.