Related Conditions
Autosomal dominant Alzheimer disease with mutation of presenilin 2(child)
Autosomal dominant Alzheimer disease with mutation of presenilin 1(child)
Autosomal dominant Alzheimer disease with mutation of amyloid precursor protein(child)
Familial disease(parent)
Primary degenerative dementia of the Alzheimer type, presenile onset(parent)
Quick Facts
- SNOMED CT
- 230265002
- UMLS CUI
- C0338445
- Fully Specified Name
- Familial Alzheimer's disease of early onset (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.