Pallister–Killian syndrome

rare disease
MedicalCondition rare_disease Q1425018
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Pallister–Killian syndrome

Summary

Pallister–Killian syndrome is a rare disease[1]. It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • Pallister–Killian syndrome's instance of is recorded as rare disease[3].
  • Pallister–Killian syndrome's instance of is recorded as developmental defect during embryogenesis[4].
  • Pallister–Killian syndrome's instance of is recorded as class of disease[5].
  • Philip David Pallister is named after Pallister–Killian syndrome[6].
  • Maria Teschler-Nicola is named after Pallister–Killian syndrome[7].
  • Pallister–Killian syndrome is a type of tetrasomy[8].
  • Pallister–Killian syndrome is a type of syndromic diaphragmatic or thoracic malformation[9].
  • Pallister–Killian syndrome is a type of chromosomal anomaly with epilepsy as a major feature[10].
  • Pallister–Killian syndrome is a type of chromosomal disease with overgrowth[11].
  • Pallister–Killian syndrome is a type of syndromic diaphragmatic or abdominal wall malformation[12].
  • Pallister–Killian syndrome is a type of syndromic anorectal malformation[13].
  • Pallister–Killian syndrome is a type of partial trisomy/tetrasomy of the short arm of chromosome 12[14].
  • Pallister–Killian syndrome's Commons category is recorded as Pallister–Killian syndrome[15].
  • Pallister–Killian syndrome's symptoms and signs is recorded as hypotonia[16].
  • Pallister–Killian syndrome's symptoms and signs is recorded as developmental language disorder[17].
  • Pallister–Killian syndrome's symptoms and signs is recorded as epilepsy[18].
  • Pallister–Killian syndrome's symptoms and signs is recorded as polydactyly[19].
  • Pallister–Killian syndrome's symptoms and signs is recorded as diaphragmatic hernia[20].
  • Pallister–Killian syndrome's ICD-9-CM is recorded as 758.81[21].
  • Pallister–Killian syndrome's NCI Thesaurus ID is recorded as C75458[22].
  • Pallister–Killian syndrome's health specialty is recorded as medical genetics[23].
  • Pallister–Killian syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_884[24].

Why It Matters

Pallister–Killian syndrome has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2] It is known by 21 alternative names across languages and contexts.[25]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . 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] . wikidata.org.
  14. [16] . flexikon.doccheck.com. Retrieved . flexikon.doccheck.com. Provenance: wikidata.org.
  15. [17] . flexikon.doccheck.com. Retrieved . flexikon.doccheck.com. Provenance: wikidata.org.
  16. [18] . flexikon.doccheck.com. Retrieved . flexikon.doccheck.com. Provenance: wikidata.org.
  17. [19] . flexikon.doccheck.com. Retrieved . flexikon.doccheck.com. Provenance: wikidata.org.
  18. [20] . flexikon.doccheck.com. Retrieved . flexikon.doccheck.com. Provenance: wikidata.org.
  19. [21] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  20. [22] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [25] . 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). Pallister–Killian syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/pallister-killian-syndrome
MLA “Pallister–Killian syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/pallister-killian-syndrome.
BibTeX @misc{4ortxyz_pallister-killian-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Pallister–Killian syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/pallister-killian-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Pallister–Killian syndrome — https://4ort.xyz/entity/pallister-killian-syndrome (retrieved 2026-05-03)

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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. 5w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Named after
    Health specialty medical genetics
    Subclass of
    Instance of rare disease, developmental defect during embryogenesis, class of disease
    + 5 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"
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