Bilateral frontoparietal polymicrogyria

medical condition
MedicalCondition developmental_defect_during_embryogenesis Q4907578
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Bilateral frontoparietal polymicrogyria

Summary

Bilateral frontoparietal polymicrogyria is a developmental defect during embryogenesis[1]. It draws 34 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #132 of 308).[2]

Key Facts

  • Bilateral frontoparietal polymicrogyria's instance of is recorded as developmental defect during embryogenesis[3].
  • Bilateral frontoparietal polymicrogyria's instance of is recorded as rare disease[4].
  • Bilateral frontoparietal polymicrogyria's instance of is recorded as class of disease[5].
  • Bilateral frontoparietal polymicrogyria is a type of polymicrogyria[6].
  • Bilateral frontoparietal polymicrogyria's NCI Thesaurus ID is recorded as C148367[7].
  • Bilateral frontoparietal polymicrogyria's genetic association is recorded as ADGRG1[8].
  • Bilateral frontoparietal polymicrogyria's genetic association is recorded as COL3A1[9].
  • Bilateral frontoparietal polymicrogyria's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101070[10].
  • Bilateral frontoparietal polymicrogyria's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_268940[11].
  • Bilateral frontoparietal polymicrogyria's has phenotype is recorded as tendon rupture[12].
  • Bilateral frontoparietal polymicrogyria's has phenotype is recorded as ligamentous laxity[13].
  • Bilateral frontoparietal polymicrogyria's has phenotype is recorded as intracranial hemorrhage[14].
  • Bilateral frontoparietal polymicrogyria's has phenotype is recorded as hypotonia[15].
  • Bilateral frontoparietal polymicrogyria's has phenotype is recorded as speech delay[16].
  • Bilateral frontoparietal polymicrogyria's has phenotype is recorded as language delay[17].
  • Bilateral frontoparietal polymicrogyria's has phenotype is recorded as bilateral talipes equinovarus[18].
  • Bilateral frontoparietal polymicrogyria's has phenotype is recorded as Neurodevelopmental delay[19].

Why It Matters

Bilateral frontoparietal polymicrogyria draws 34 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #132 of 308).[2]

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] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . Bilateral frontoparietal polymicrogyria, Lennox-Gastaut syndrome, and GPR56 gene mutations. wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  7. [9] . Type III collagen (COL3A1): Gene and protein structure, tissue distribution, and associated diseases.. wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . Vascular Ehlers-Danlos Syndrome in siblings with biallelic COL3A1 sequence variants and marked clinical variability in the extended family. wikidata.org.
  11. [13] . Biallelic COL3A1 mutations result in a clinical spectrum of specific structural brain anomalies and connective tissue abnormalities. wikidata.org.
  12. [14] . Biallelic COL3A1 mutations result in a clinical spectrum of specific structural brain anomalies and connective tissue abnormalities. wikidata.org.
  13. [15] . Biallelic COL3A1 mutations result in a clinical spectrum of specific structural brain anomalies and connective tissue abnormalities. wikidata.org.
  14. [16] . Biallelic COL3A1 mutations result in a clinical spectrum of specific structural brain anomalies and connective tissue abnormalities. wikidata.org.
  15. [17] . Biallelic COL3A1 mutations result in a clinical spectrum of specific structural brain anomalies and connective tissue abnormalities. wikidata.org.
  16. [18] . Type III collagen (COL3A1): Gene and protein structure, tissue distribution, and associated diseases.. wikidata.org.
  17. [19] . Type III collagen (COL3A1): Gene and protein structure, tissue distribution, and associated diseases.. wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). Bilateral frontoparietal polymicrogyria. Retrieved May 3, 2026, from https://4ort.xyz/entity/bilateral-frontoparietal-polymicrogyria
MLA “Bilateral frontoparietal polymicrogyria.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/bilateral-frontoparietal-polymicrogyria.
BibTeX @misc{4ortxyz_bilateral-frontoparietal-polymicrogyria_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Bilateral frontoparietal polymicrogyria}}, year = {2026}, url = {https://4ort.xyz/entity/bilateral-frontoparietal-polymicrogyria}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Bilateral frontoparietal polymicrogyria — https://4ort.xyz/entity/bilateral-frontoparietal-polymicrogyria (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. 22d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id MONDO_0011738
    Orphanet id 101070
    Imported from
    Mesh descriptor id C564652
    + 15 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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