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Up to: Familial amyotrophic lateral sclerosis · Frontotemporal dementia with motor neuron disease · Frontotemporal dementia and/or amyotrophic lateral sclerosis
Frontotemporal dementia and/or amyotrophic lateral sclerosis 2
An 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.
This condition has no sub-types.