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parietal foramina

Human disease
MedicalCondition hereditary_disorder Q18987133
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parietal foramina

Summary

parietal foramina is a hereditary disorder[1].

Key Facts

  • parietal foramina's instance of is recorded as hereditary disorder[2].
  • parietal foramina's instance of is recorded as rare disease[3].
  • parietal foramina's instance of is recorded as class of disease[4].
  • parietal foramina is a type of neural tube defect[5].
  • parietal foramina's anatomical location is recorded as Parietal foramen[6].
  • parietal foramina's genetic association is recorded as MSX2[7].
  • parietal foramina's genetic association is recorded as ALX4[8].
  • parietal foramina's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060285[9].
  • parietal foramina's exact match is recorded as http://identifiers.org/doid/DOID:0060285[10].
  • parietal foramina's exact match is recorded as http://purl.obolibrary.org/obo/HP_0002697[11].
  • parietal foramina's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_60015[12].
  • parietal foramina's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  7. [8] ↑ . The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  8. [9] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [10] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  10. [11] ↑ . Human Phenotype Ontology release 2018-03-08. Retrieved . wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . 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). parietal foramina. Retrieved May 3, 2026, from https://4ort.xyz/entity/parietal-foramina
MLA “parietal foramina.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/parietal-foramina.
BibTeX @misc{4ortxyz_parietal-foramina_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{parietal foramina}}, year = {2026}, url = {https://4ort.xyz/entity/parietal-foramina}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): parietal foramina — https://4ort.xyz/entity/parietal-foramina (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/parietal-foramina · 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. 16d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0018953
    Orphanet id → 60015
    Imported from → —
    Mesh descriptor id → C566826
    + 14 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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