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amyotrophic lateral sclerosis type 6 | RareConnect | RareConnect.io

/familial amyotrophic lateral sclerosis

/frontotemporal dementia with motor neuron disease

/amyotrophic lateral sclerosis type 6

amyotrophic lateral sclerosis type 6

Rare Disease

MONDO:0011951

Also Known As

ALS6FUS amyotrophic lateral sclerosisamyotrophic lateral sclerosis 6, with or without frontotemporal dementiaamyotrophic lateral sclerosis caused by mutation in FUSautosomal recessive amyotrophic lateral sclerosis 6amyotrophic lateral sclerosis 6 with or without frontotemporal dementia

Definition

Any amyotrophic lateral sclerosis in which the cause of the disease is a mutation in the FUS 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:608030 ↗

GARD

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