periventricular nodular heterotopia

congenital nervous system abnormality characterized by non proper migration of neurons during the early development of the fetal brain
MedicalCondition rare_disease Q18553263
Press Enter · cited answer in seconds

periventricular nodular heterotopia

Summary

periventricular nodular heterotopia is a rare disease[1].

Key Facts

  • periventricular nodular heterotopia's instance of is recorded as rare disease[2].
  • periventricular nodular heterotopia's instance of is recorded as class of disease[3].
  • periventricular nodular heterotopia's subclass of is recorded as nervous system malformations[4].
  • periventricular nodular heterotopia's subclass of is recorded as gray matter heterotopia[5].
  • periventricular nodular heterotopia's subclass of is recorded as nodular neuronal heterotopia[6].
  • periventricular nodular heterotopia's MeSH descriptor ID is recorded as D054091[7].
  • periventricular nodular heterotopia's OMIM ID is recorded as 300049[8].
  • periventricular nodular heterotopia's OMIM ID is recorded as 608097[9].
  • periventricular nodular heterotopia's OMIM ID is recorded as 608098[10].
  • periventricular nodular heterotopia's OMIM ID is recorded as 612881[11].
  • periventricular nodular heterotopia's OMIM ID is recorded as 615544[12].
  • periventricular nodular heterotopia's KEGG ID is recorded as H00270[13].
  • periventricular nodular heterotopia's MeSH tree code is recorded as C10.500.507.450.750[14].
  • periventricular nodular heterotopia's MeSH tree code is recorded as C16.131.666.507.450.750[15].
  • periventricular nodular heterotopia's Disease Ontology ID is recorded as DOID:0050454[16].
  • periventricular nodular heterotopia's Orphanet ID is recorded as 98892[17].
  • periventricular nodular heterotopia's NCI Thesaurus ID is recorded as C202072[18].
  • periventricular nodular heterotopia's health specialty is recorded as neurology[19].
  • periventricular nodular heterotopia's genetic association is recorded as FLNA[20].
  • periventricular nodular heterotopia's genetic association is recorded as NEDD4L[21].
  • periventricular nodular heterotopia's genetic association is recorded as ERMARD[22].
  • periventricular nodular heterotopia's genetic association is recorded as ARFGEF2[23].
  • periventricular nodular heterotopia's genetic association is recorded as ARF1[24].
  • periventricular nodular heterotopia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050454[25].
  • periventricular nodular heterotopia's exact match is recorded as http://identifiers.org/doid/DOID:0050454[26].

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] . Disease Ontology. Retrieved . wikidata.org.
  4. [5] . Integration of gray matter nodules into functional cortical circuits in periventricular heterotopia. wikidata.org.
  5. [6] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [8] . Disease Ontology. Retrieved . wikidata.org.
  8. [9] . Disease Ontology. Retrieved . wikidata.org.
  9. [10] . Disease Ontology. Retrieved . wikidata.org.
  10. [11] . Disease Ontology. Retrieved . wikidata.org.
  11. [12] . Disease Ontology. Retrieved . wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . Disease Ontology. Retrieved . wikidata.org.
  16. [17] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  20. [21] . Mutations in the HECT domain of NEDD4L lead to AKT-mTOR pathway deregulation and cause periventricular nodular heterotopia. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  21. [22] . Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene. wikidata.org.
  22. [23] . Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex. wikidata.org.
  23. [24] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  24. [25] . Disease Ontology. Retrieved . wikidata.org.
  25. [26] . Identifiers.org. registry.identifiers.org. Provenance: 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). periventricular nodular heterotopia. Retrieved May 3, 2026, from https://4ort.xyz/entity/periventricular-nodular-heterotopia
MLA “periventricular nodular heterotopia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/periventricular-nodular-heterotopia.
BibTeX @misc{4ortxyz_periventricular-nodular-heterotopia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{periventricular nodular heterotopia}}, year = {2026}, url = {https://4ort.xyz/entity/periventricular-nodular-heterotopia}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): periventricular nodular heterotopia — https://4ort.xyz/entity/periventricular-nodular-heterotopia (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/periventricular-nodular-heterotopia · Last refreshed: