Status: current, Primitive. Date: 31-Jul 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4576214016 | Autosomal dominant Alzheimer disease with mutation of presenilin 1 | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
4576888018 | Autosomal dominant Alzheimer disease due to mutation of presenilin 1 (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
4576889014 | Autosomal dominant Alzheimer disease due to mutation of presenilin 1 | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant Alzheimer disease due to mutation of presenilin 1 | Has interpretation | Impaired | true | Inferred relationship | Some | 2 | |
Autosomal dominant Alzheimer disease due to mutation of presenilin 1 | Associated morphology | Degenerative abnormality | true | Inferred relationship | Some | 1 | |
Autosomal dominant Alzheimer disease due to mutation of presenilin 1 | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant Alzheimer disease due to mutation of presenilin 1 | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some | ||
Autosomal dominant Alzheimer disease due to mutation of presenilin 1 | Interprets | Cognitive functions | true | Inferred relationship | Some | 2 | |
Autosomal dominant Alzheimer disease due to mutation of presenilin 1 | Is a | Familial Alzheimer's disease of early onset | true | Inferred relationship | Some | ||
Autosomal dominant Alzheimer disease due to mutation of presenilin 1 | Finding site | Structure of cerebrum | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Mental health disorder reference set
Problem/Diagnosis reference set