C214864Level 8
Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 4
**Semantic type:** Disease or Syndrome
**Definition:** An autosomal dominant form of frontotemporal dementia and/or amyotrophic lateral sclerosis caused by mutation(s) in the TBK1 gene, encoding serine/threonine-protein kinase TBK1.
**Synonyms:** - FTDALS4
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