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parietal foramina

Human disease
Class type of: neural tube defect, hereditary disorder Q18987133

Facts

9 properties
Instance of
rare disease, class of disease[4]
Subclass of
neural tube defect, hereditary disorder
Age of onset
congenital onset, neonatal onset[9][10]
Anatomical location
Parietal foramen[5]
Genetic association
MSX2, ALX4[7][8]
Has phenotype
parietal foramina, vomiting, headache, Venous malformation, cleft palate, Short clavicles, disability affecting intellectual abilities, seizure, craniosynostosis, encephalocele, myelomeningocele, hereditary multiple exostoses, Congenital craniofacial dysostosis, encephalomalacia, cleft lip[12][13][14][15][16][17][18][19][20][21][22][23][24][25]
On focus list of Wikimedia project
WikiProject Medicine[11]
P14914
D60015[26]
Prevalence
+0.00005[6]
🏷️ Also known as
en Caitlin marks en Catlin marks en enlarged parietal foramina en Fenestrae parietales symmetricae en Foramina parietalia permagna en hereditary cranium bifidum en parietal foramina en Symmetric parietal foramina es Foramina parietal fr lacunes pariétales
🔖 Identifiers · 11
Disease Ontology ID
DOID:0060285
Exact match
purl.obolibrary.org, identifiers.org, purl.obolibrary.org, www.orpha.net
Human Phenotype Ontology ID
HP:0002697
ICD-10-CM
Q75.8
ICD-11 ID (Foundation)
905361904
KEGG ID
H00475
MeSH descriptor ID
C566826
Mondo ID
MONDO_0018953
OMIM ID
610k (168k–610k, n=3)
Orphanet ID
60015
UMLS CUI
C1868598, C0222706, C4280556

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Summary

parietal foramina is a rare disease[1]. It is a type of neural tube defect[2] and hereditary disorder[3].

References

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

Direct Wikidata claims

  1. [4] ↑ . wikidata.org.
  2. [2] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [3] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . Retrieved . 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] ↑ . Retrieved . wikidata.org.
  9. [10] ↑ . Retrieved . wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . Retrieved . wikidata.org.
  12. [13] ↑ . Retrieved . wikidata.org.
  13. [14] ↑ . Retrieved . wikidata.org.
  14. [15] ↑ . Retrieved . wikidata.org.
  15. [16] ↑ . Retrieved . wikidata.org.
  16. [17] ↑ . Retrieved . wikidata.org.
  17. [18] ↑ . Retrieved . wikidata.org.
  18. [19] ↑ . Retrieved . wikidata.org.
  19. [20] ↑ . Retrieved . wikidata.org.
  20. [21] ↑ . Retrieved . wikidata.org.
  21. [22] ↑ . Retrieved . wikidata.org.
  22. [23] ↑ . Retrieved . wikidata.org.
  23. [24] ↑ . Retrieved . wikidata.org.
  24. [25] ↑ . Retrieved . wikidata.org.
  25. [26] ↑ . 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 November 6, 2026, from https://4ort.xyz/entity/parietal-foramina
MLA “parietal foramina.” 4ort.xyz Knowledge Graph, 4ort.xyz, 6 Nov. 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: 2026-11-06}}
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 2026-11-06)

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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. 16d ago · ACorrêa (WMB) · 2026-10-24 view diff on Wikidata ↗
    Sitelink count → 1
    Prevalence → {'amount': '+0.00005'}
    Wikipedia languages → ['de']
    Age of onset → congenital onset, neonatal onset
    + 3 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||pt, pt-br */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61469|batch #61469]]: Raras.org data import"
  2. 18w 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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