C168752Level 9
Amyotrophic Lateral Sclerosis 10, 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 TARDBP gene, encoding TAR DNA-binding protein 43.
**Synonyms:** - ALS10
GET
/api/v1/systems/nci_thesaurus/nodes/C168752Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.