Alzheimer's Disease 1

Preferred Label : Alzheimer's Disease 1;

NCIt synonyms : AD1; Familial Alzheimer's Disease, Type 1;

NCIt definition : Alzheimer's disease caused by mutation(s) in the APP gene, encoding amyloid-beta A4 protein. The onset of this condition typically occurs before age 65.;

Details

Origin ID

C146894;

UMLS CUI

C1863052;

Automatic exact mappings (from CISMeF team)
- Alzheimer disease, familial, 1 [OMIM Phenotype]
- Alzheimer's disease 1 [DO Concept]
- alzheimer disease type 1 [MeSH Supplementary Concept]
- alzheimer disease, familial, 1 [MeSH concept]
Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Alzheimer disease, familial, 1 [OMIM Phenotype]
- alzheimer disease type 1 [MeSH Supplementary Concept]
- alzheimer disease, familial, 1 [MeSH concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]
disease_mapped_to_gene
- APP Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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