Alzheimer disease 10

Preferred Label : Alzheimer disease 10;

CISMeF acronym : AD10;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Alzheimer disease, familial, 10; AD10;

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

Inheritance : Autosomal dominant;

Prefixed ID : %609636;

Details

Origin ID

609636;

UMLS CUI

C1864828;

Currated CISMeF NLP mapping
- Alzheimer's disease 10 [DO Concept]
- alzheimer disease 10 [MeSH concept]
- alzheimer disease 10 [MeSH Supplementary Concept]
DO Cross reference
- Alzheimer's disease 10 [DO Concept]
HPO term(s)
- Alzheimer disease [HPO term]
- Autosomal dominant inheritance [HPO term]
- Cerebral cortical atrophy [HPO term]
- Dementia [HPO term]
- Memory impairment [HPO term]
- Neurological speech impairment [HPO term]
- Personality changes [HPO term]
ORDO concept(s)
- Early-onset autosomal dominant Alzheimer disease [ORDO Disease]
See also inter- (CISMeF)
- ADAM10 wt Allele [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Alzheimer's disease 10 [DO Concept]
- alzheimer disease 10 [MeSH Supplementary Concept]
- alzheimer disease 10 [MeSH concept]

Keyword's position in hierarchy(ies) :

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