Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology

Preferred Label : Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %605055;

Details

Origin ID

605055;

UMLS CUI

C1857933;

Currated CISMeF NLP mapping
- alzheimer disease, familial Early-Onset, with coexisting amyloid and prion pathology [MeSH Supplementary Concept]
- alzheimer disease, familial Early-Onset, with coexisting amyloid and prion pathology [MeSH concept]
HPO term(s)
- Alzheimer disease [HPO term]
- Autosomal dominant inheritance [HPO term]
- Cerebral cortex with spongiform changes [HPO term]
- Neurofibrillary tangles [HPO term]
- Seizure [HPO term]
- Senile plaques [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 disease, familial Early-Onset, with coexisting amyloid and prion pathology [MeSH Supplementary Concept]
- alzheimer disease, familial Early-Onset, with coexisting amyloid and prion pathology [MeSH concept]

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