OMOP Concept 608060
Autosomal dominant Alzheimer disease due to mutation of presenilin 2
StandardConditionSNOMED1156798001Disorder
Maps from
0
Descendants
0
Valid from
31 Jul 2021
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Autosomal dominant Alzheimer disease due to mutation of presenilin 2 across source vocabularies.
- Autosomal dominant Alzheimer disease due to mutation of presenilin 2 (disorder)
- Autosomal dominant Alzheimer disease with mutation of presenilin 2
- enfermedad de Alzheimer autosómica dominante con mutación de presenilina 2
- enfermedad de Alzheimer autosómica dominante debida a mutación de presenilina 2
- enfermedad de Alzheimer autosómica dominante debida a mutación de presenilina 2 (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(33)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Familial Alzheimer's disease of early onset
- 1Hereditary degenerative disease of central nervous system
- 2Autosomal hereditary disorder
- 2Degenerative disease of the central nervous system
- 2Familial disease
- 2Hereditary disorder of nervous system
- 2Primary degenerative dementia of the Alzheimer type, presenile onset
- 3Alzheimer's disease
- 3Degenerative disorder
- 3Disease
- 3Disorder of nervous system
- 3Disorder of the central nervous system
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Presenile dementia
- 4Central nervous system finding
- 4Cerebral degeneration presenting primarily with dementia
- 4Clinical finding
- 4Dementia
- 4Disorder of body system
- 4Genetic disease
- 5Cerebral degeneration
- 5Impaired cognition
- 5Organic mental disorder
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