Fatal familial insomnia (Q38207): Difference between revisions

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+https://id.who.int/icd/entity/669154658
@@ Property / Canonical URI: https://id.who.int/icd/entity/669154658 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:8E02.2
@@ Property / CURIE: CID11:8E02.2 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-8E02.2
@@ Property / Canary Token: dki-india-8E02.2 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
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+https://pauloleads.com.br/cases-publicos/
+Normal 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
-Calendar
+Gregorian
-Precision
+day
 Before
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@@ Property / Collection date: 13 August 2026 / rank @@
+Normal rank
@@ 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, caused by inheritance of mutation(s) of normal prion protein genes. This disease is characterised by severe insomnia and autonomic system dysfunction, and is fatal. Confirmation is by pathological examination of the brain and genetic testing.

Language	Label	Description	Also known as
default for all languages	8E02.2
English	Fatal familial insomnia	A disease of the brain, caused by inheritance of mutation(s) of normal prion protein genes. This disease is characterised by severe insomnia and autonomic system dysfunction, and is fatal. Confirmation is by pathological examination of the brain and genetic testing.