Mowat-Wilson syndrome

rare genetic disorder
MedicalCondition developmental_defect_during_embryogenesis Q2757585
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Mowat-Wilson syndrome

Summary

Mowat-Wilson syndrome is a developmental defect during embryogenesis[1]. It draws 253 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #88 of 308).[2]

Key Facts

  • Mowat-Wilson syndrome's instance of is recorded as developmental defect during embryogenesis[3].
  • Mowat-Wilson syndrome's instance of is recorded as designated intractable/rare disease[4].
  • Mowat-Wilson syndrome's instance of is recorded as rare disease[5].
  • Mowat-Wilson syndrome's instance of is recorded as class of disease[6].
  • Mowat-Wilson syndrome is a type of syndrome[7].
  • Mowat-Wilson syndrome is a type of Hirschsprung's disease[8].
  • Mowat-Wilson syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[9].
  • Mowat-Wilson syndrome is a type of syndromic intestinal malformation[10].
  • Mowat-Wilson syndrome is a type of genetic syndromic intellectual disability[11].
  • Mowat-Wilson syndrome is a type of genetic disease[12].
  • Mowat-Wilson syndrome's Commons category is recorded as Mowat–Wilson syndrome[13].
  • Mowat-Wilson syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4594[14].
  • Mowat-Wilson syndrome's ICD-9-CM is recorded as 759.89[15].
  • Mowat-Wilson syndrome's NCI Thesaurus ID is recorded as C74999[16].
  • Mowat-Wilson syndrome's genetic association is recorded as ZEB2[17].
  • Mowat-Wilson syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060485[18].
  • Mowat-Wilson syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060485[19].
  • Mowat-Wilson syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].

Why It Matters

Mowat-Wilson syndrome draws 253 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #88 of 308).[2] It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[21] It is known by 13 alternative names across languages and contexts.[22]

References

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

Direct Wikidata claims

  1. [3] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . Disease Ontology. Retrieved . 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] . Disease Ontology. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  13. [15] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  14. [16] . Disease Ontology. Retrieved . wikidata.org.
  15. [17] . Q905695. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  16. [18] . Disease Ontology. Retrieved . wikidata.org.
  17. [19] . Identifiers.org. ebi.ac.uk. Provenance: wikidata.org.
  18. [20] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [21] . Wikidata sitelinks. wikidata.org.
  3. [22] . 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). Mowat-Wilson syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/mowat-wilson-syndrome
MLA “Mowat-Wilson syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/mowat-wilson-syndrome.
BibTeX @misc{4ortxyz_mowat-wilson-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Mowat-Wilson syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/mowat-wilson-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Mowat-Wilson syndrome — https://4ort.xyz/entity/mowat-wilson-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. 7w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Genetic association ZEB2
    Subclass of
    Instance of developmental defect during embryogenesis, designated intractable/rare disease, rare disease +1
    Instance of
    + 3 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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