Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3760372011 | Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3760373018 | Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3760374012 | RVCL - retinal vasculopathy cerebral leukoencephalopathy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3760375013 | RVCL-S - retinal vasculopathy, cerebral leukoencephalopathy, systemic manifestations | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3866554012 | RVCL-S - retinal vasculopathy, cerebral leucoencephalopathy, systemic manifestations | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3866555013 | RVCL - retinal vasculopathy cerebral leucoencephalopathy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3866556014 | Retinal vasculopathy with cerebral leucoencephalopathy and systemic manifestations | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3760376014 | An inherited group of small vessel diseases comprised of cerebroretinal vasculopathy (CRV), hereditary vascular retinopathy (HRV) and hereditary endotheliopathy with retinopathy, nephropathy and stroke all exhibiting progressive visual impairment as well as variable cerebral dysfunction. There is evidence the disease is caused by heterozygous mutation in the TREX1 gene on chromosome 3p21. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Glomerular disease | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Hereditary disorder of the visual system (disorder) | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Hereditary disorder of immune system | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Small vessel cerebrovascular disease (disorder) | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Chronic disease of cardiovascular system | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Autoimmune disease | false | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Chronic brain syndrome | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Disorder of capillaries (disorder) | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Leukoencephalopathy | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Hereditary nephropathy (disorder) | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Renal vascular disorder | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Retinal vascular disorder (disorder) | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Chronic disease of genitourinary system | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Chronic disease of immune function (disorder) | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Finding site | Structure of blood vessel of retina (body structure) | true | Inferred relationship | Some | 3 | |
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Pathological process (attribute) | Autoimmune process | false | Inferred relationship | Some | 6 | |
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Clinical course | Progressive (qualifier value) | true | Inferred relationship | Some | 1 | |
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Finding site | Cerebral white matter structure | true | Inferred relationship | Some | 5 | |
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Finding site | Cerebrovascular system structure | true | Inferred relationship | Some | 2 | |
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Finding site | Structure of glomerular capillary basement membrane | true | Inferred relationship | Some | 4 | |
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Type I interferonopathy | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Is a | Chronic disease of immune structure (disorder) | true | Inferred relationship | Some | ||
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Finding site | Structure of immune system (body structure) | true | Inferred relationship | Some | 6 | |
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Associated morphology | Inflammatory morphology (morphologic abnormality) | true | Inferred relationship | Some | 6 | |
| Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations | Pathological process (attribute) | Abnormal immune process (qualifier value) | true | Inferred relationship | Some | 6 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR