C214859Level 9
Amyotrophic Lateral Sclerosis 26, with or without Frontotemporal Dementia
**Semantic type:** Disease or Syndrome
**Definition:** An autosomal dominant form of amyotrophic lateral sclerosis caused by mutation(s) in the TIA1 gene, encoding cytotoxic granule associated RNA binding protein TIA1.
**Synonyms:** - ALS26
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