Alzheimer disease 2

Preferred Label : Alzheimer disease 2;

Symbol : AD2;

CISMeF acronym : AD2;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Alzheimer disease 2, late-onset; Alzheimer disease associated with apoe4;

Inheritance : Autosomal dominant allele (19q) with additional multifactorial component in late-onset cases;

Prefixed ID : #104310;

Details

Origin ID

104310;

UMLS CUI

C1863051;

Currated CISMeF NLP mapping
- Alzheimer disease type 2 [MeSH concept]
- Alzheimer's disease 2 [DO Concept]
- alzheimer disease type 2 [MeSH Supplementary Concept]
DO Cross reference
- Alzheimer's disease 2 [DO Concept]
Genes related to phenotype
- Apolipoprotein e [OMIM gene]
HPO term(s)
- Alzheimer disease [HPO term]
- Autosomal dominant inheritance [HPO term]
- Dementia [HPO term]
- Late onset [HPO term]
- Long-tract signs [HPO term]
- Neurofibrillary tangles [HPO term]
- Neurofibrillary tangles composed of disordered microtubules in neurons [HPO term]
- Parkinsonism [HPO term]
ORDO concept(s)
- Alzheimer disease [ORDO Disease]
- Early-onset autosomal dominant Alzheimer disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Alzheimer disease type 2 [MeSH concept]
- Alzheimer's disease 2 [DO Concept]
- Familial Alzheimer's disease of late onset (disorder) [SNOMED CT concept]
- alzheimer disease type 2 [MeSH Supplementary Concept]
Validated automatic mappings to NTBT
- Alzheimer disease [ORDO Disease]
- Dementia in Alzheimers disease with early onset [ICD-10 Sub-category (who)]

Keyword's position in hierarchy(ies) :

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