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 |
| 3323687017 | Hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3323688010 | Hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3323689019 | HERNS syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3323690011 | HERNS (hereditary endotheliopathy, retinopathy, nephropathy, stroke) syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3323691010 | A phenotypic variant of a group of inherited small vessel disorders known as retinal vasculopathy and cerebral leukodystrophy and characterized by strokes, vision loss, pseudotumors, seizures, motor and sensory deficits, headaches and occasionally renal disease. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3323692015 | A phenotypic variant of a group of inherited small vessel disorders known as retinal vasculopathy and cerebral leucodystrophy and characterised by strokes, vision loss, pseudotumours, seizures, motor and sensory deficits, headaches and occasionally renal disease. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | Is a | Autosomal dominant hereditary disorder | false | Inferred relationship | Some | ||
| Hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | Is a | Retinal vascular disorder (disorder) | false | Inferred relationship | Some | ||
| Hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | Is a | Cardiovascular system hereditary disorder | false | Inferred relationship | Some | ||
| Hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | Is a | Hereditary disorder of the visual system (disorder) | false | Inferred relationship | Some | ||
| Hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome | Finding site | Structure of blood vessel of retina (body structure) | 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