Frontotemporal dementia due to CHMP2B mutation (Q99473): Difference between revisions

← Older edit

@@ Property / Canonical URI @@
+https://id.who.int/icd/entity/1752271020
@@ Property / Canonical URI: https://id.who.int/icd/entity/1752271020 / rank @@
+Normal rank
@@ Property / CURIE @@
+CID11:ID_1752271020
@@ Property / CURIE: CID11:ID_1752271020 / rank @@
+Normal rank
@@ Property / Canary Token @@
+dki-india-ID_1752271020
@@ Property / Canary Token: dki-india-ID_1752271020 / rank @@
+Normal rank
@@ Property / Verification Status @@
+Concluído
@@ Property / Verification Status: Concluído / rank @@
+Normal rank
@@ Property / Knowledge Architect @@
+https://pauloleads.com.br/cases-publicos/
+Normal rank
@@ Property / Collection date @@
+August 2026Timestamp +2026-08-15T00:00:00Z
Timezone +00:00
Calendar Gregorian
Precision 1 day
Before 0
After 0
-Timestamp
++2026-08-15T00:00:00Z
-Timezone
++00:00
-Calendar
+Gregorian
-Precision
+day
 Before
 After
@@ Property / Collection date: 15 August 2026 / rank @@
+Normal rank

Latest revision as of 16:08, 16 August 2026

A rare genetic FTD due to a mutation in the gene encoding charged multivesicular body protein 2B on chromosome 3. It can present as a behavioural syndrome. It can also be associated with motor neuron disease.

Language	Label	Description	Also known as
default for all languages	ID_1752271020
English	Frontotemporal dementia due to CHMP2B mutation	A rare genetic FTD due to a mutation in the gene encoding charged multivesicular body protein 2B on chromosome 3. It can present as a behavioural syndrome. It can also be associated with motor neuron disease.