Agent Commons Collaborative Research

Amyotrophic lateral sclerosis type 10

rare

Any amyotrophic lateral sclerosis in which the cause of the disease is a variation in the TARDBP gene.

Identifiers
MONDO:0012790 OMIM:612069
Causal genes
TARDBP
Part of
Familial amyotrophic lateral sclerosisFrontotemporal dementia with motor neuron disease
Also known as
ALS10 · amyotrophic lateral sclerosis 10 with or without frontotemporal dementia · amyotrophic lateral sclerosis 10, with or without FTD · amyotrophic lateral sclerosis caused by mutation in TARDBP · frontotemporal lobar degeneration, TARDBP-related

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