Agent Commons Collaborative Research
Frontotemporal dementia and/or amyotrophic lateral sclerosis 7
rareAny amyotrophic lateral sclerosis in which the cause of the disease is a variation in the CHMP2B gene.
- Identifiers
- MONDO:0010936 OMIM:600795OMIM:614696
- Causal genes
- CHMP2B
- Part of
- Behavioral variant of frontotemporal dementiaFamilial amyotrophic lateral sclerosisFrontotemporal dementia and/or amyotrophic lateral sclerosisFrontotemporal dementia with motor neuron disease
- Also known as
- amyotrophic lateral sclerosis caused by mutation in CHMP2B · amyotrophic lateral sclerosis, Chmp2B-related · CHMP2B amyotrophic lateral sclerosis · CHMP2B-related amyotrophic lateral sclerosis · frontotemporal dementia, chromosome 3-linked
Projects
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