Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7

Preferred Label : Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 7;

NCIt synonyms : FTDALS7;

NCIt definition : An autosomal dominant form of frontotemporal dementia and/or amyotrophic lateral sclerosis caused by mutation(s) in the CHMP2B gene, encoding charged multivesicular body protein 2b.;

Détails

Origin ID

C214863;

Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
disease_mapped_to_gene
- CHMP2B Gene [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients