World Of Taxonomy
C214855Level 9

Amyotrophic Lateral Sclerosis 15, with or without Frontotemporal Dementia

**Semantic type:** Disease or Syndrome

**Definition:** An X-linked dominant form of amyotrophic lateral sclerosis caused by mutation(s) in the UBQLN2 gene, encoding ubiquilin-2.

**Synonyms:** - ALS15

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