omphalocele

physical disorder characterized by a defect in the development of the abdominal wall muscles, resulting in the intestines, liver and other organs to remain outside of the abdomen in a sac
MedicalCondition class_of_disease Q1521567
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Summary

omphalocele is a class of disease[1]. omphalocele draws 104 Wikipedia views per month (class_of_disease category, ranking #522 of 1,968).[2]

Key Facts

  • omphalocele's instance of is recorded as class of disease[3].
  • omphalocele is a type of congenital disorder[4].
  • omphalocele is a type of abdominal wall defect[5].
  • omphalocele's Commons category is recorded as Omphalocele[6].
  • omphalocele's ICD-9-CM is recorded as 756.72[7].
  • omphalocele's NCI Thesaurus ID is recorded as C98997[8].
  • omphalocele's health specialty is recorded as medical genetics[9].
  • omphalocele's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060327[10].
  • omphalocele's exact match is recorded as http://identifiers.org/doid/DOID:0060327[11].
  • omphalocele's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].

Why It Matters

omphalocele draws 104 Wikipedia views per month (class_of_disease category, ranking #522 of 1,968).[2] omphalocele has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[13] omphalocele is known by 19 alternative names across languages and contexts.[14]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [11] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  10. [12] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [13] ↑ . Wikidata sitelinks. wikidata.org.
  3. [14] ↑ . 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). omphalocele. Retrieved October 14, 2026, from https://4ort.xyz/entity/omphalocele
MLA “omphalocele.” 4ort.xyz Knowledge Graph, 4ort.xyz, 14 Oct. 2026, https://4ort.xyz/entity/omphalocele.
BibTeX @misc{4ortxyz_omphalocele_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{omphalocele}}, year = {2026}, url = {https://4ort.xyz/entity/omphalocele}, note = {Accessed: 2026-10-14}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): omphalocele — https://4ort.xyz/entity/omphalocele (retrieved 2026-10-14)

Canonical URL: https://4ort.xyz/entity/omphalocele · 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. 10d ago · عُثمان · 2026-10-04 view diff on Wikidata ↗
    Wikipedia languages → ['ar', 'commons', 'de', 'en', 'es', 'fa', 'fr', 'hy', 'id', 'it', 'ja', 'or', 'p
    Human phenotype ontology id → HP:0001539
    Claims rich → —
    "/* wbsetclaim-create:1||1 */ Human phenotype ontology id: HP:0001539, Matched to [[:toollabs:mix-n-match/#/entry/19254192|Omphalocele (#19254192)]] in [[:toollabs:mix-n-match/#/catalog/405|HPO]] #mix'"
  2. 14w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of → congenital disorder, abdominal wall defect
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39732|batch #39732]]: rm redundant subclass"
  3. 21w ago · Twofivesixbot bot · 2026-05-17 view diff on Wikidata ↗
    Instance of → —
    Health specialty → medical genetics
    Aliases → —
    Subclass of → congenital disorder, abdominal wall defect
    + 3 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-update-qualifiers:1||1|5 */ Yso id: 39361, mv to monolingual text names on YSO statements"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.