Status: retired, 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 |
| 3323683018 | Hereditary vascular retinopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3323684012 | Hereditary vascular retinopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 50008311000188111 | rétinopathie vasculaire héréditaire | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 797731000241114 | rétinopathie vasculaire héréditaire (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3323685013 | A phenotypic variant of a group of inherited small vessel disorders known as retinal vasculopathy and cerebral leukodystrophy and characterized by progressive visual impairment, strokes and often associated with Raynaud phenomenon and migraine-like symptoms. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3323686014 | A phenotypic variant of a group of inherited small vessel disorders known as retinal vasculopathy and cerebral leucodystrophy and characterised by progressive visual impairment, strokes and often associated with Raynaud phenomenon and migraine-like symptoms. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary vascular retinopathy (disorder) | est un(e) (attribut) | Autosomal dominant hereditary disorder | false | Inferred relationship | Some | ||
| Hereditary vascular retinopathy (disorder) | est un(e) (attribut) | trouble vasculaire rétinien | false | Inferred relationship | Some | ||
| Hereditary vascular retinopathy (disorder) | est un(e) (attribut) | Cardiovascular system hereditary disorder | false | Inferred relationship | Some | ||
| Hereditary vascular retinopathy (disorder) | est un(e) (attribut) | Hereditary disorder of the visual system | false | Inferred relationship | Some | ||
| Hereditary vascular retinopathy (disorder) | localisation d'une constatation (attribut) | Structure of blood vessel of retina | false | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Concept inactivation indicator reference set
REPLACED BY association reference set (foundation metadata concept)
FHIR