Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 2

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal dominant form of frontotemporal dementia and/or amyotrophic lateral sclerosis caused by mutation(s) in the CHCHD10 gene, encoding coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial.

**Synonyms:** - FTDALS2