Status: retired, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3323683018 | Hereditary vascular retinopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3323684012 | Hereditary vascular retinopathy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary vascular retinopathy | Is a | Autosomal dominant hereditary disorder | false | Inferred relationship | Existential restriction modifier | ||
| Hereditary vascular retinopathy | Is a | Retinal vascular disorder | false | Inferred relationship | Existential restriction modifier | ||
| Hereditary vascular retinopathy | Is a | Cardiovascular system hereditary disorder | false | Inferred relationship | Existential restriction modifier | ||
| Hereditary vascular retinopathy | Is a | Hereditary disorder of the visual system | false | Inferred relationship | Existential restriction modifier | ||
| Hereditary vascular retinopathy | Finding site | Structure of blood vessel of retina | false | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR