Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3324649018 | Familial Alzheimer-like prion disease (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3324650018 | Familial Alzheimer-like prion disease | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3324651019 | An exceedingly rare form of prion disease with characteristics of neuropathological features of Alzheimer disease including memory impairment and depression, related to abnormal prion protein (PrP) caused by a gene mutation in PRNP. Patients present with a prolonged, atypical course (absence of myoclonus or ataxia) unlike other forms of prion disease, with severe neurofibrillary tangle pathology and high levels of cerebral amyloidosis. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 889841000172114 | maladie à prions familiale Alzheimer-like | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 945251000172111 | maladie à prions familiale type Alzheimer | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial Alzheimer-like prion disease (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Familial Alzheimer-like prion disease (disorder) | Is a | Prion disease | true | Inferred relationship | Some | ||
| Familial Alzheimer-like prion disease (disorder) | Is a | Familial disease | true | Inferred relationship | Some | ||
| Familial Alzheimer-like prion disease (disorder) | Is a | Hereditary disorder of nervous system | false | Inferred relationship | Some | ||
| Familial Alzheimer-like prion disease (disorder) | Associated morphology | Spongy degeneration | true | Inferred relationship | Some | 1 | |
| Familial Alzheimer-like prion disease (disorder) | Causative agent | Prion | true | Inferred relationship | Some | 1 | |
| Familial Alzheimer-like prion disease (disorder) | Finding site | Brain tissue structure | true | Inferred relationship | Some | 1 | |
| Familial Alzheimer-like prion disease (disorder) | Pathological process (attribute) | Infectious process (qualifier value) | true | Inferred relationship | Some | 1 | |
| Familial Alzheimer-like prion disease (disorder) | Is a | Hereditary degenerative disease of central nervous system | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets