Home › Entities › developmental_defect_during_embryogenesis › Bardet-Biedl syndrome 18

Bardet-Biedl syndrome 18

Bardet-Biedl syndrome that has material basis in homozygous mutation in the BBIP1 gene on chromosome 10q25
MedicalCondition developmental_defect_during_embryogenesis Q27674845
Press Enter · cited answer in seconds

Summary

Bardet-Biedl syndrome 18 is a developmental defect during embryogenesis[1]. It is known by 4 alternative names across languages and contexts.[2]

Key Facts

  • Instance of: rare disease[3], class of disease[4]
  • Subclass of: Bardet-Biedl syndrome[5]
  • Health specialty: medical genetics[6]
  • Genetic association: BBIP1[7]
  • Exact match: http://purl.obolibrary.org/obo/DOID_0110140[8], http://identifiers.org/doid/DOID:0110140[9]
  • On focus list of Wikimedia project: WikiProject Medicine[10]

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] ↑ . Disease Ontology. Retrieved . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . UniProt. Retrieved . wikidata.org.
  6. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [9] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  8. [10] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . 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). Bardet-Biedl syndrome 18. Retrieved May 3, 2026, from https://4ort.xyz/entity/bardet-biedl-syndrome-18
MLA “Bardet-Biedl syndrome 18.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/bardet-biedl-syndrome-18.
BibTeX @misc{4ortxyz_bardet-biedl-syndrome-18_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Bardet-Biedl syndrome 18}}, year = {2026}, url = {https://4ort.xyz/entity/bardet-biedl-syndrome-18}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Bardet-Biedl syndrome 18 — https://4ort.xyz/entity/bardet-biedl-syndrome-18 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/bardet-biedl-syndrome-18 · 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. 15w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0014446
    Genetic association → BBIP1
    Uniprot disease id → DI-04077
    Instance of → developmental defect during embryogenesis, rare disease, class of disease
    + 10 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.