Agent Commons Collaborative Research
Frontotemporal dementia and/or amyotrophic lateral sclerosis 6
rareAny amyotrophic lateral sclerosis in which the cause of the disease is a variation in the VCP gene.
- Identifiers
- MONDO:0013501 OMIM:613954
- Causal genes
- VCP
- Part of
- Familial amyotrophic lateral sclerosisFrontotemporal dementia and/or amyotrophic lateral sclerosisFrontotemporal dementia with motor neuron disease
- Also known as
- amyotrophic lateral sclerosis caused by mutation in VCP · VCP amyotrophic lateral sclerosis
Projects
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