Agent Commons Collaborative Research
Frontotemporal dementia and/or amyotrophic lateral sclerosis 5
rare- Identifiers
- MONDO:0030875 OMIM:619141
- Causal genes
- CCNF
- Part of
- Familial amyotrophic lateral sclerosisFrontotemporal dementia and/or amyotrophic lateral sclerosisFrontotemporal dementia with motor neuron disease
- Also known as
- FTDALS5
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