Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3007510013 | Familial cerebral saccular aneurysm (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3007838010 | Familial cerebral saccular aneurysm | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5013733015 | Familial intracranial saccular aneurysm | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5013734014 | Familial berry aneurysm | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5013727012 | A rare genetic neurovascular malformation characterized by sac-like bulging of cerebral arteries due to weakening of the endothelial layer. Familial occurrence is suspected when two or more affected first- to third-degree relatives are present in a family. Aneurysms may remain asymptomatic throughout life, or rupture and thereby cause potentially life-threatening subarachnoid hemorrhage. Patients with familial cerebral saccular aneurysm are more likely to develop more than one brain aneurysm, are at greater risk of rupture, and tend to have poorer outcome after rupture than patients with sporadic cerebral aneurysms. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5013898018 | A rare genetic neurovascular malformation characterised by sac-like bulging of cerebral arteries due to weakening of the endothelial layer. Familial occurrence is suspected when two or more affected first- to third-degree relatives are present in a family. Aneurysms may remain asymptomatic throughout life, or rupture and thereby cause potentially life-threatening subarachnoid haemorrhage. Patients with familial cerebral saccular aneurysm are more likely to develop more than one brain aneurysm, are at greater risk of rupture, and tend to have poorer outcome after rupture than patients with sporadic cerebral aneurysms. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial cerebral saccular aneurysm (disorder) | Is a | Intracranial aneurysm | false | Inferred relationship | Some | ||
| Familial cerebral saccular aneurysm (disorder) | Associated morphology | Saccular aneurysm | true | Inferred relationship | Some | 1 | |
| Familial cerebral saccular aneurysm (disorder) | Finding site | Structure of intracranial artery | true | Inferred relationship | Some | 1 | |
| Familial cerebral saccular aneurysm (disorder) | Is a | Berry aneurysm | true | Inferred relationship | Some | ||
| Familial cerebral saccular aneurysm (disorder) | Is a | Familial disease | true | Inferred relationship | Some | ||
| Familial cerebral saccular aneurysm (disorder) | Is a | Autosomal hereditary disorder | true | Inferred relationship | Some | ||
| Familial cerebral saccular aneurysm (disorder) | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR