Variant Creutzfeldt-Jakob Disease (Q38206): Difference between revisions

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+https://id.who.int/icd/entity/378572696
@@ Property / Canonical URI: https://id.who.int/icd/entity/378572696 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:8E01.2
@@ Property / CURIE: CID11:8E01.2 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-8E01.2
@@ Property / Canary Token: dki-india-8E01.2 / rank @@
+Normal rank
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+Concluído
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+https://pauloleads.com.br/cases-publicos/
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+August 2026Timestamp +2026-08-13T00:00:00Z
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Calendar Gregorian
Precision 1 day
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 Before
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@@ Property / Collection date: 13 August 2026 / rank @@
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@@ Property / Linked ICD 10 @@
+A81.9
@@ Property / Linked ICD 10: A81.9 / rank @@
+Normal rank

Latest revision as of 02:56, 13 August 2026

A disease of the brain, that is suspected to be caused by a prion associated with Bovine Spongiform Encephalopathy. This disease is characterised by a long incubation period, psychiatric symptoms followed by neurological deficits, and is fatal. Transmission may be by ingestion of food (with a bovine origin) contaminated with infected brain or spinal cord from an infected cow, or blood transfusion. Confirmation is by pathological examination of the brain.

Language	Label	Description	Also known as
default for all languages	8E01.2
English	Variant Creutzfeldt-Jakob Disease	A disease of the brain, that is suspected to be caused by a prion associated with Bovine Spongiform Encephalopathy. This disease is characterised by a long incubation period, psychiatric symptoms followed by neurological deficits, and is fatal. Transmission may be by ingestion of food (with a bovine origin) contaminated with infected brain or spinal cord from an infected cow, or blood transfusion. Confirmation is by pathological examination of the brain.