Frontotemporal Dementia-1

Preferred Label : Frontotemporal Dementia-1;

NCIt synonyms : FTDP17; Frontotemporal Dementia with Parkinsonism-17; FTD1;

NCIt definition : An autosomal dominant subtype of frontotemporal dementia caused by mutation(s) in the MAPT gene, encoding microtubule-associated protein tau.;

Détails

Origin ID

C217087;

Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]
disease_has_primary_anatomic_site
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
disease_mapped_to_gene
- MAPT 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