Frontotemporal dementia due to VCP mutation (Q99478): Difference between revisions
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dki-india-ID_1650171830 | |||||||||||||||
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15 August 2026
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Latest revision as of 16:08, 16 August 2026
FTD due to mutations in the valosin-containing protein on chromosome 9. It is also associated with inclusion body myositis and Paget's disease of the bone, as well as motor neuron disease. Neuropathologically there are ubiquitin positive inclusions
| Language | Label | Description | Also known as |
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| default for all languages | ID_1650171830 |
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| English | Frontotemporal dementia due to VCP mutation |
FTD due to mutations in the valosin-containing protein on chromosome 9. It is also associated with inclusion body myositis and Paget's disease of the bone, as well as motor neuron disease. Neuropathologically there are ubiquitin positive inclusions |
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CID11:ID_1650171830
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dki-india-ID_1650171830
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Concluído
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15 August 2026
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