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epilepsy syndrome

complex of signs and symptoms that define a unique epileptic condition
Class type of: rare genetic epilepsy, epilepsy Q55785625

Facts

4 properties
Instance of
Wikimedia list article, class of disease[2]
Subclass of
rare genetic epilepsy, epilepsy[3][4]
Genetic association
STARD7, SLC7A6OS, GABRB1, AARS1, ADORA2A, AP3B2, ATP6V1A, FRRS1L, CACNA1A, CACNA2D1, SCARB2, CHRNA2, CSTB, CELF2, DMXL2, DNM1, EEF1A2, EPM2A, GABRA2, GABRA5, GABRB3, GABRG2, GNAO1, GOSR2, GRIN1, GRIN2A, GRIN2B, GRIN2D, HCN1, KCNA2, KCNB1, KCNC1, KCNC2, KCNMA1, KCNQ2, KCNQ3, MAPK10, MECP2, TRNH, TRNK, TRNS1, SERPINI1, SCN1A, SCN2A, SCN3A, SCN8A, SEMA6B, SLC25A12, GLUT1, SLC6A1, SPTAN1, SYNGAP1, TNRC6A, YWHAG, SLC12A5, PRDM8, NPRL3, TRIM8, PLCB1, EFHC1, PRICKLE1, CPA6, ARX, DEPDC5, KCNT1, CDK19, NHLRC1, KCTD7, SLC13A5, PACS2, NECAP1, NPRL2, YEATS2, SZT2, FBXO28, TBC1D24, PRRT2, MARCHF6, SAMD12[6][7][8][9][10][11][12][13][14][15][16][17][18][19]
Is a list of
epilepsy[5]
🏷️ Also known as
en epileptic syndromes en epilepsy syndrome en epileptic syndrome en list of epilepsy syndromes en syndromic epilepsy ar متلازمات الصرع fr syndrome épileptique
🔖 Identifiers · 10
OpenAlex ID
C2778734009
Exact match
www.orpha.net
MeSH descriptor ID
D000073376
MeSH tree code
C10.228.140.490.493
Microsoft Academic ID (discontinued)
2778734009
Mondo ID
MONDO_0015650
Orphanet ID
166463
Raras disease ID
D166463
UMLS CUI
C0391958, C4505072
Wellcome Collection concept ID
p9qzurkv

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Summary

epilepsy syndrome is a Wikimedia list article[1].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . Retrieved . wikidata.org.
  6. [7] ↑ . Retrieved . wikidata.org.
  7. [8] ↑ . Retrieved . wikidata.org.
  8. [9] ↑ . Retrieved . wikidata.org.
  9. [10] ↑ . Retrieved . wikidata.org.
  10. [11] ↑ . Retrieved . 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.

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). epilepsy syndrome. Retrieved November 8, 2026, from https://4ort.xyz/entity/epilepsy-syndrome
MLA “epilepsy syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 8 Nov. 2026, https://4ort.xyz/entity/epilepsy-syndrome.
BibTeX @misc{4ortxyz_epilepsy-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{epilepsy syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/epilepsy-syndrome}, note = {Accessed: 2026-11-08}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): epilepsy syndrome — https://4ort.xyz/entity/epilepsy-syndrome (retrieved 2026-11-08)

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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. 18d ago · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Raras disease ID → D166463
    Genetic association → STARD7, SLC7A6OS, GABRB1 +1
    "Changed labels, descriptions, aliases and claims: QuickStatements 3.0 batch #61469: Raras.org data import"
  2. 18w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    UMLS CUI → C0391958, C4505072
    Microsoft Academic ID (discontinued) → 2778734009
    Is a list of → epilepsy
    Orphanet ID → 166463
    + 9 other properties edited (see Wikidata diff for full list)
    "Changed the item: QuickStatements 3.0 batch #39953: deprecate redundant disease superclasses (2)"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.