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bifid uvula

Bifid uvula is a fissure type embryopathy affecting the uvula at the back of the soft palate
Class type of: cleft palate, rare genetic developmental defect during embryogenesis, developmental defect during embryogenesis Q4002938

Facts

5 properties
Instance of
class of disease
Subclass of
cleft palate, rare genetic developmental defect during embryogenesis, developmental defect during embryogenesis[2][3][4]
Age of onset
infantile onset, neonatal onset[7][8]
Genetic association
UBB, GRHL3[5][6]
Has phenotype
bifid uvula, Wikidata item, Submucous cleft soft palate, cleft lip[9][10][11][12]
🏷️ Also known as
en Bifidity of the uvula en bifid uvula en UVULA, BIFID en Uvula, Cleft en Uvular cleft es uvula bifida es úvula bífida fr luette bifide he ענבל חצוי it ugola bifida
🔖 Identifiers · 11
Exact match
www.orpha.net
Google Knowledge Graph ID
/g/121_5cf5
Human Phenotype Ontology ID
HP:0000193
ICD-10-CM
Q35.7
ICD-11 ID (Foundation)
684398038
ICD-11 ID (MMS)
LA42.2
Mondo ID
MONDO_0008637
OMIM ID
192100
Orphanet ID
99771
Raras disease ID
D99771
UMLS CUI
C0266122, C4551488

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Summary

bifid uvula is a class of disease[1].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [5] ↑ . Retrieved . wikidata.org.
  5. [6] ↑ . Retrieved . wikidata.org.
  6. [7] ↑ . Retrieved . 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.

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). bifid uvula. Retrieved November 6, 2026, from https://4ort.xyz/entity/bifid-uvula
MLA “bifid uvula.” 4ort.xyz Knowledge Graph, 4ort.xyz, 6 Nov. 2026, https://4ort.xyz/entity/bifid-uvula.
BibTeX @misc{4ortxyz_bifid-uvula_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{bifid uvula}}, year = {2026}, url = {https://4ort.xyz/entity/bifid-uvula}, note = {Accessed: 2026-11-06}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): bifid uvula — https://4ort.xyz/entity/bifid-uvula (retrieved 2026-11-06)

Canonical URL: https://4ort.xyz/entity/bifid-uvula · 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. 18d ago · ACorrêa (WMB) · 2026-10-24 view diff on Wikidata ↗
    Genetic association → UBB, GRHL3
    Age of onset → infantile onset, neonatal onset
    Has phenotype → bifid uvula, Wikidata item, Submucous cleft soft palate
    Raras disease ID → D99771
    "Changed labels, descriptions, aliases and claims: QuickStatements 3.0 batch #61469: Raras.org data import"
  2. 18d ago · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Human Phenotype Ontology ID → HP:0000193
    "Changed the item: QuickStatements 3.0 batch #61242: HPO ID through mesh or umls"
  3. 18w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo ID → MONDO_0008637
    Orphanet ID → 99771
    Google Knowledge Graph ID → /g/121_5cf5
    Instance of → class of disease
    + 9 other properties edited (see Wikidata diff for full list)
    "Changed the item: QuickStatements 3.0 batch #39742: subclass of disease, not instance"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.