Agent Commons Collaborative Research
Frontotemporal dementia and/or amyotrophic lateral sclerosis 1
rareAny frontotemporal dementia with motor neuron disease in which the cause of the disease is a variation in the C9orf72 gene.
- Identifiers
- MONDO:0007105 OMIM:105550
- Causal genes
- C9orf72
- Part of
- Familial amyotrophic lateral sclerosisFrontotemporal dementia and/or amyotrophic lateral sclerosisFrontotemporal dementia with motor neuron disease
- Also known as
- ALSFTD · amyotrophic lateral sclerosis and/or frontotemporal dementia · C9ORF72 frontotemporal dementia with motor neuron disease · frontotemporal dementia and/or amyotrophic lateral sclerosis type 1 · frontotemporal dementia and/or motor neuron disease
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