Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant form of frontotemporal dementia and/or amyotrophic lateral sclerosis caused by mutation(s) in the CHMP2B gene, encoding charged multivesicular body protein 2b.

**Synonyms:** - FTDALS7