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frontotemporal dementia and/or amyotrophic lateral sclerosis 7 | RareConnect | RareConnect.io

/familial amyotrophic lateral sclerosis

/behavioral variant of frontotemporal dementia

/frontotemporal dementia and/or amyotrophic lateral sclerosis

/frontotemporal dementia and/or amyotrophic lateral sclerosis 7

frontotemporal dementia and/or amyotrophic lateral sclerosis 7

Rare Disease

MONDO:0010936

Also Known As

CHMP2B amyotrophic lateral sclerosisCHMP2B-related amyotrophic lateral sclerosisFTD3amyotrophic lateral sclerosis caused by mutation in CHMP2Bamyotrophic lateral sclerosis, Chmp2B-relatedfrontotemporal dementia, chromosome 3-linkedDmt1dementia, familial nonspecific

Definition

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

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:600795 ↗OMIM:614696 ↗

GARD

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