Pai syndrome

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

MedicalCondition head_and_neck_disease Q47461585

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Pai syndrome

Summary

Pai syndrome is a head and neck disease^[1].

Key Facts

Pai syndrome's instance of is recorded as head and neck disease^[2].
Pai syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
Pai syndrome's instance of is recorded as class of disease^[4].
Pai syndrome is a type of midface dysplasia^[5].
Pai syndrome is a type of orofacial clefting syndrome^[6].
Pai syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1993^[7].

⭐ Popularity Graph

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Quick Facts

Instance of class of disease

Subclass of midface dysplasia, orofacial clefting syndrome, developmental defect during embryogenesis, head and neck disease

Properties

Exact match www.orpha.net

External References (8)

Gard rare disease id 3439

Icd-10-cm Q87.8

Icd-11 id (foundation) 1236130516

Mesh descriptor id C536135

Mondo id MONDO_0007956

Omim id 155145

Orphanet id 1993

Umls cui C1835087

References

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

Direct Wikidata claims

[2] ↑ Pai syndrome — instance of (P31): head and neck disease. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[3] ↑ Pai syndrome — instance of (P31): developmental defect during embryogenesis. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[4] ↑ Pai syndrome — instance of (P31): class of disease. wikidata.org.
[5] ↑ Pai syndrome — subclass of (P279): midface dysplasia. wikidata.org.
[6] ↑ Pai syndrome — subclass of (P279): orofacial clefting syndrome. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[7] ↑ Pai syndrome — exact match (P2888): http://www.orpha.net/ORDO/Orphanet_1993. wikidata.org.

Class ancestry

[1] ↑ Pai syndrome is an instance of head and neck disease (Q55789477) [P31, primary]. Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). Pai syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/pai-syndrome

MLA “Pai syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 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: 2026-05-03}}

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 2026-05-03)

Canonical URL: https://4ort.xyz/entity/pai-syndrome · Last refreshed: May 3, 2026

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.

19d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗

Mondo id → MONDO_0007956

Gard rare disease id → 3439

Orphanet id → 1993

Instance of → head and neck disease, developmental defect during embryogenesis, class of disease

+ 9 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.