Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
5071804017 | Familial isolated retinal arterial tortuosity (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5071805016 | Familial isolated retinal arterial tortuosity | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5071806015 | Retinal hemorrhage with vascular tortuosity | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5071807012 | Tortuosity of retinal arteries | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5071808019 | Retinal haemorrhage with vascular tortuosity | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5071809010 | Retinal arteriolar tortuosity | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5071811018 | A rare genetic cerebral small vessel disease with isolated marked tortuosity of second order and third order retinal arteries with normal first order arteries and venous system, typically located in the macular and peripapillary area and developing during childhood or early adulthood. The disease may be asymptomatic, although most patients present variable degrees of transient vision loss due to retinal hemorrhage following physical exertion or minor trauma. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5071812013 | A rare genetic cerebral small vessel disease with isolated marked tortuosity of second order and third order retinal arteries with normal first order arteries and venous system, typically located in the macular and peripapillary area and developing during childhood or early adulthood. The disease may be asymptomatic, although most patients present variable degrees of transient vision loss due to retinal haemorrhage following physical exertion or minor trauma. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial isolated retinal arterial tortuosity (disorder) | Is a | Retinal arterial tortuosity | true | Inferred relationship | Some | ||
Familial isolated retinal arterial tortuosity (disorder) | Is a | Tortuosity of systemic artery (disorder) | true | Inferred relationship | Some | ||
Familial isolated retinal arterial tortuosity (disorder) | Is a | Disease of non-coronary systemic artery | true | Inferred relationship | Some | ||
Familial isolated retinal arterial tortuosity (disorder) | Is a | Retinal vascular disorder (disorder) | true | Inferred relationship | Some | ||
Familial isolated retinal arterial tortuosity (disorder) | Is a | Deformity of eyeball | true | Inferred relationship | Some | ||
Familial isolated retinal arterial tortuosity (disorder) | Is a | Genetic disease | true | Inferred relationship | Some | ||
Familial isolated retinal arterial tortuosity (disorder) | Finding site | Structure of retinal artery | true | Inferred relationship | Some | 1 | |
Familial isolated retinal arterial tortuosity (disorder) | Associated morphology | Tortuosity | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set