alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques

Preferred Label : alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques;

MeSH note : mutation in PSEN1;

Origin ID

C564329;

UMLS CUI

C1843014;

Automatic exact mappings (from CISMeF team)
- Alzheimer disease 3 [OMIM Phenotype]
MeSH term(s) associated for indexing
- alzheimer disease [MeSH Descriptor]
- paraparesis, spastic [MeSH Descriptor]
Record concept(s)
- alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]