Frontotemporal dementia due to CHMP2B mutation (Q99473): Difference between revisions
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15 August 2026
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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 |
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| 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. |
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CID11:ID_1752271020
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dki-india-ID_1752271020
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Concluído
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15 August 2026
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