familial hemiplegic migraine

migraine with aura that is characterized by temporary numbness or weakness, often affecting one side of the body
MedicalCondition rare_disease Q3312899
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familial hemiplegic migraine

Summary

familial hemiplegic migraine is a rare disease[1]. It draws 22 Wikipedia views per month (rare_disease category, ranking #216 of 627).[2]

Key Facts

  • familial hemiplegic migraine's instance of is recorded as rare disease[3].
  • familial hemiplegic migraine's instance of is recorded as class of disease[4].
  • familial hemiplegic migraine's subclass of is recorded as migraine with aura[5].
  • familial hemiplegic migraine's subclass of is recorded as hemiplegic migraine[6].
  • familial hemiplegic migraine's OMIM ID is recorded as 141500[7].
  • familial hemiplegic migraine's OMIM ID is recorded as 602481[8].
  • familial hemiplegic migraine's OMIM ID is recorded as 609634[9].
  • familial hemiplegic migraine's DiseasesDB is recorded as 4693[10].
  • familial hemiplegic migraine's Freebase ID is recorded as /m/025s_x7[11].
  • familial hemiplegic migraine's KEGG ID is recorded as H00775[12].
  • familial hemiplegic migraine's GeneReviews ID is recorded as NBK1388[13].
  • familial hemiplegic migraine's eMedicine ID is recorded as 1142731[14].
  • familial hemiplegic migraine's Disease Ontology ID is recorded as DOID:0060178[15].
  • familial hemiplegic migraine's symptoms and signs is recorded as muscle weakness[16].
  • familial hemiplegic migraine's symptoms and signs is recorded as mental confusion[17].
  • familial hemiplegic migraine's symptoms and signs is recorded as somnolence[18].
  • familial hemiplegic migraine's symptoms and signs is recorded as hemiparesis[19].
  • familial hemiplegic migraine's Orphanet ID is recorded as 569[20].
  • familial hemiplegic migraine's ICD-9-CM is recorded as 346.8[21].
  • familial hemiplegic migraine's NCI Thesaurus ID is recorded as C117009[22].
  • familial hemiplegic migraine's health specialty is recorded as neurology[23].
  • familial hemiplegic migraine's genetic association is recorded as CACNA1A[24].
  • familial hemiplegic migraine's genetic association is recorded as SCN1A[25].
  • familial hemiplegic migraine's genetic association is recorded as ATP1A2[26].
  • familial hemiplegic migraine's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060178[27].

Why It Matters

familial hemiplegic migraine draws 22 Wikipedia views per month (rare_disease category, ranking #216 of 627).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] It is known by 4 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . Disease Ontology. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . Disease Ontology. Retrieved . wikidata.org.
  6. [8] . Disease Ontology. Retrieved . wikidata.org.
  7. [9] . Disease Ontology. Retrieved . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . Freebase Data Dumps. wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Disease Ontology. Retrieved . wikidata.org.
  14. [16] . Disease Ontology. Retrieved . wikidata.org.
  15. [17] . Disease Ontology. Retrieved . wikidata.org.
  16. [18] . Disease Ontology. Retrieved . wikidata.org.
  17. [19] . Disease Ontology. Retrieved . wikidata.org.
  18. [20] . Disease Ontology. Retrieved . wikidata.org.
  19. [21] . Disease Ontology. Retrieved . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. wikidata.org.
  23. [25] . Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine. wikidata.org.
  24. [26] . Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2. wikidata.org.
  25. [27] . Disease Ontology. Retrieved . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . 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). familial hemiplegic migraine. Retrieved May 3, 2026, from https://4ort.xyz/entity/familial-hemiplegic-migraine
MLA “familial hemiplegic migraine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/familial-hemiplegic-migraine.
BibTeX @misc{4ortxyz_familial-hemiplegic-migraine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{familial hemiplegic migraine}}, year = {2026}, url = {https://4ort.xyz/entity/familial-hemiplegic-migraine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): familial hemiplegic migraine — https://4ort.xyz/entity/familial-hemiplegic-migraine (retrieved 2026-05-03)

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