Dravet syndrome

epilepsy characterized by frequent febrile seizures and with onset before 1 year
MedicalCondition designated_intractable_rare_disease Q1255956
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Dravet syndrome

Summary

Dravet syndrome is a designated intractable/rare disease[1]. It draws 311 Wikipedia views per month (designated_intractable_rare_disease category, ranking #68 of 201).[2]

Key Facts

  • Dravet syndrome's instance of is recorded as designated intractable/rare disease[3].
  • Dravet syndrome's instance of is recorded as rare disease[4].
  • Dravet syndrome's instance of is recorded as class of disease[5].
  • Charlotte Dravet is named after Dravet syndrome[6].
  • Dravet syndrome's subclass of is recorded as generalized epilepsy with febrile seizures plus[7].
  • Dravet syndrome's subclass of is recorded as Ohtahara syndrome[8].
  • Dravet syndrome's OMIM ID is recorded as 607208[9].
  • Dravet syndrome's ICD-9 ID is recorded as 345.1[10].
  • Dravet syndrome's DiseasesDB is recorded as 33728[11].
  • Dravet syndrome's Freebase ID is recorded as /m/0h0275[12].
  • Dravet syndrome's KEGG ID is recorded as H01818[13].
  • Dravet syndrome's GeneReviews ID is recorded as NBK1318[14].
  • Dravet syndrome's Disease Ontology ID is recorded as DOID:0080422[15].
  • Dravet syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4744[16].
  • Dravet syndrome's Orphanet ID is recorded as 33069[17].
  • Dravet syndrome's BBC Things ID is recorded as aeaeeea7-3aca-448f-aaa7-7f40d47b3d13[18].
  • Dravet syndrome's NCI Thesaurus ID is recorded as C116573[19].
  • Dravet syndrome's health specialty is recorded as neurology[20].
  • Dravet syndrome's genetic association is recorded as SCN1A[21].
  • Dravet syndrome's genetic association is recorded as GABRA1[22].
  • Dravet syndrome's genetic association is recorded as STXBP1[23].
  • Dravet syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060171[24].
  • Dravet syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060171[25].
  • Dravet syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080422[26].
  • Dravet syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080422[27].

Why It Matters

Dravet syndrome draws 311 Wikipedia views per month (designated_intractable_rare_disease category, ranking #68 of 201).[2] It has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[28] It is known by 20 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] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . Disease Ontology. Retrieved . wikidata.org.
  7. [9] . Disease Ontology. Retrieved . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . Freebase Data Dumps. wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Disease Ontology. Retrieved . wikidata.org.
  14. [16] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  15. [17] . Disease Ontology. Retrieved . wikidata.org.
  16. [18] . BBC Things. wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  20. [22] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  21. [23] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  22. [24] . Disease Ontology. Retrieved . wikidata.org.
  23. [25] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  24. [26] . Disease Ontology. Retrieved . wikidata.org.
  25. [27] . Identifiers.org. registry.identifiers.org. Provenance: 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). Dravet syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/dravet-syndrome
MLA “Dravet syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/dravet-syndrome.
BibTeX @misc{4ortxyz_dravet-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Dravet syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/dravet-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Dravet syndrome — https://4ort.xyz/entity/dravet-syndrome (retrieved 2026-05-03)

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