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
GET
/api/v1/systems/nci_thesaurus/nodes/C214855Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.