Genetic or presumed genetic syndromes primarily expressed as epilepsy (Q41220): Difference between revisions

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+https://id.who.int/icd/entity/517052870
@@ Property / Canonical URI: https://id.who.int/icd/entity/517052870 / rank @@
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@@ Property / CURIE @@
+CID11:8A61
@@ Property / CURIE: CID11:8A61 / rank @@
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@@ Property / Canary Token: dki-india-8A61 / rank @@
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+August 2026Timestamp +2026-08-13T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
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++2026-08-13T00:00:00Z
-Timezone
++00:00
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@@ Property / Collection date: 13 August 2026 / rank @@
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@@ Property / Linked ICD 10 @@
+G40.0
@@ Property / Linked ICD 10: G40.0 / rank @@
+Normal rank

Latest revision as of 07:18, 13 August 2026

The epilepsy is, as best as understood, the direct result of one or more known or presumed genetic defects in which seizures are the core symptom of the disorder.

Language	Label	Description	Also known as
default for all languages	8A61
English	Genetic or presumed genetic syndromes primarily expressed as epilepsy	The epilepsy is, as best as understood, the direct result of one or more known or presumed genetic defects in which seizures are the core symptom of the disorder.