Frontotemporal dementia due to CHMP2B mutation (Q99473): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Canary Token | |||
dki-india-ID_1752271020 | |||
| Property / Canary Token: dki-india-ID_1752271020 / rank | |||
Normal rank | |||
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. |
Statements
CID11:ID_1752271020
0 references
dki-india-ID_1752271020
0 references
