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.

Also known as: FTDALS2, frontotemporal dementia and/or amyotrophic lateral sclerosis 2, frontotemporal dementia and/or amyotrophic lateral sclerosis type 2

20 clinical trials for this condition and its sub-types.