Alzheimer disease 5

Preferred Label : Alzheimer disease 5;

CISMeF acronym : AD5;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Alzheimer disease, familial, 5; AD5;

Description : For a phenotypic description and a discussion of genetic heterogeneity of Alzheimer disease (AD), see 104300.;

Inheritance : Autosomal dominant;

Prefixed ID : %602096;

Détails

Origin ID

602096;

UMLS CUI

C1865868;

Automatic exact mappings (from CISMeF team)
- AD 5 [MeSH Supplementary Concept]
- Presenilin-2 [NCIt concept]
Currated CISMeF NLP mapping
- Alzheimer's disease 5 [DO Concept]
- alzheimer disease 5 [MeSH concept]
- alzheimer disease 5 [MeSH Supplementary Concept]
DO Cross reference
- Alzheimer's disease 5 [DO Concept]
HPO term(s)
- Alzheimer disease [HPO term]
- Autosomal dominant inheritance [HPO term]
- Late onset [HPO term]
- Late-onset form of familial Alzheimer disease [HPO term]
ORDO concept(s)
- Early-onset autosomal dominant Alzheimer disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Alzheimer's disease 5 [DO Concept]
- alzheimer disease 5 [MeSH Supplementary Concept]
- alzheimer disease 5 [MeSH concept]

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

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