Frontotemporal dementia and/or amyotrophic lateral sclerosis 7

MONDO:0010936

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the CHMP2B gene.

Also known as: CHMP2B amyotrophic lateral sclerosis, CHMP2B-related amyotrophic lateral sclerosis, FTD3, amyotrophic lateral sclerosis caused by mutation in CHMP2B, amyotrophic lateral sclerosis, Chmp2B-related, frontotemporal dementia, chromosome 3-linked, Dmt1, dementia, familial nonspecific

30 clinical trials for this condition and its sub-types, 0 tagged with Frontotemporal dementia and/or amyotrophic lateral sclerosis 7 itself.

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↑ Behavioral variant of frontotemporal dementia (42) ↑ Familial amyotrophic lateral sclerosis (29) ↑ Frontotemporal dementia and/or amyotrophic lateral sclerosis (5)

Including sub-types (30) Tagged with Frontotemporal dementia and/or amyotrophic lateral sclerosis 7 (0)

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