Pai syndrome

Median cleft of the upper lip-corpus callosum lipoma-cutaneous polyps syndrome

Facts

5 properties
Instance of
class of disease
Subclass of
midface dysplasia, orofacial clefting syndrome, developmental defect during embryogenesis, head and neck disease
Age of onset
congenital onset, neonatal onset[7][8]
Prevalence
+0.000001[6]
🏷️ Also known as
en CLEFT, MEDIAN, OF UPPER LIP WITH POLYPS OF FACIAL SKIN AND NASAL MUCOSA en Median cleft of the upper lip-corpus callosum lipoma-cutaneous polyps syndrome en Median cleft of upper lip with polyps of facial skin and nasal mucosa en Pai syndrome fr syndrome de Pai
🔖 Identifiers · 10
Exact match
www.orpha.net
GARD rare disease ID
3439
ICD-10-CM
Q87.8
ICD-11 ID (Foundation)
1236130516
MeSH descriptor ID
C536135
OMIM ID
155145
Orphanet ID
1993
Raras disease ID
D01993
UMLS CUI
C1835087

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Summary

Pai syndrome is a class of disease[1]. It is a type of midface dysplasia[2], orofacial clefting syndrome[3], developmental defect during embryogenesis[4], and head and neck disease[5].

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] ↑ . Monarch Disease Ontology release 2018-06-29. 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.
  12. [13] ↑ . Retrieved . wikidata.org.
  13. [14] ↑ . Retrieved . wikidata.org.
  14. [15] ↑ . Retrieved . wikidata.org.
  15. [16] ↑ . Retrieved . wikidata.org.
  16. [17] ↑ . 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). Pai syndrome. Retrieved November 9, 2026, from https://4ort.xyz/entity/pai-syndrome
MLA “Pai syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 9 Nov. 2026, https://4ort.xyz/entity/pai-syndrome.
BibTeX @misc{4ortxyz_pai-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Pai syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/pai-syndrome}, note = {Accessed: 2026-11-09}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Pai syndrome — https://4ort.xyz/entity/pai-syndrome (retrieved 2026-11-09)

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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. 17d ago · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Prevalence → 0.000001
    Age of onset → congenital onset, neonatal onset
    Has phenotype → Median cleft upper lip, cleft palate, skin tag +1
    Raras disease ID → D01993
    "Changed labels, descriptions, aliases and claims: QuickStatements 3.0 batch #61469: Raras.org data import"
  2. 18w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo ID → MONDO_0007956
    GARD rare disease ID → 3439
    Orphanet ID → 1993
    Instance of → class of disease
    + 8 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.