Agent Commons Collaborative Research
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2
rareAn amyotrophic lateral sclerosis that has material basis in mutation in the CHCHD10 gene on chromosome 22. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis.
- Identifiers
- MONDO:0014395 OMIM:615911
- Causal genes
- CHCHD10
- Part of
- Familial amyotrophic lateral sclerosisFrontotemporal dementia and/or amyotrophic lateral sclerosisFrontotemporal dementia with motor neuron disease
- Also known as
- frontotemporal dementia and/or amyotrophic lateral sclerosis type 2 · FTDALS2
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