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Concept information

... > Clinical finding (finding) > disease > Genetic disease > Hereditary disease > Autosomal hereditary disorder > Dominant hereditary disorder, NOS > Autosomal dominant Alzheimer disease with mutation of presenilin 2

Preferred term

Autosomal dominant Alzheimer disease with mutation of presenilin 2  

Type

  • http://www.irandoc.ac.ir/onto/irandoc-meta/Concept

Associated morphology

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Has interpretation

Is a

URI

http://www.irandoc.acir/onto/irandoc/1156798001

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