Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1771702019 | Hereditary cutaneous vascular syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 1782786013 | Hereditary cutaneous vascular syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary cutaneous vascular syndrome | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary cutaneous vascular syndrome | Finding site | Structure of cardiovascular system | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hereditary neurocutaneous angiomata | Is a | True | Hereditary cutaneous vascular syndrome | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR