Frontotemporal dementia and/or amyotrophic lateral sclerosis 2

MONDO:0014395

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

21 clinical trials for this condition and its sub-types, 0 tagged with Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 itself.

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↑ Familial amyotrophic lateral sclerosis (29) ↑ Frontotemporal dementia with motor neuron disease (19) ↑ Frontotemporal dementia and/or amyotrophic lateral sclerosis (5)

Including sub-types (21) Tagged with Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 (0)

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