familial alzheimer disease (FAD)

Preferred Label : familial alzheimer disease (FAD);

CISMeF acronym : FAD;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0584546;

UMLS CUI

C0276496;

Automatic exact mappings (from CISMeF team)
- BRCA2 DNA repair associated [ORDO Gene]
- BRCA2 wt Allele [NCIt concept]
- FA complementation group D2 [ORDO Gene]
- FANCD2 wt Allele [NCIt concept]
- Flavin adenine dinucleotide [LOINC component]
- MAF bZIP transcription factor [ORDO Gene]
- PSEN1 wt Allele [NCIt concept]
- macrophage activating factor [SNOMED Notion]
- presenilin 1 [ORDO Gene]
- riboflavin dinucleotide [SNOMED Notion]
- transmissible virus dementia [SNOMED Notion]
Related record
- alzheimer disease [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Early-onset autosomal dominant Alzheimer disease [ORDO Disease]