Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2013. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2923300016 | Hereditary dysplasia of blood vessel (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 2923303019 | Hereditary dysplasia of blood vessel | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary dysplasia of blood vessel | Is a | Disorder of blood vessel | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary dysplasia of blood vessel | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Hereditary dysplasia of blood vessel | Finding site | Blood vessel structure | true | Inferred relationship | Existential restriction modifier | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Osler hemorrhagic telangiectasia syndrome | Is a | True | Hereditary dysplasia of blood vessel | Inferred relationship | Existential restriction modifier | |
| Klippel-Trenaunay-Weber syndrome | Is a | False | Hereditary dysplasia of blood vessel | Inferred relationship | Existential restriction modifier | |
| Idiopathic arterial calcification of infancy | Is a | True | Hereditary dysplasia of blood vessel | Inferred relationship | Existential restriction modifier | |
| Arterial tortuosity syndrome | Is a | True | Hereditary dysplasia of blood vessel | Inferred relationship | Existential restriction modifier | |
| Progressive arterial occlusive disease, hypertension, heart defect, bone fragility, brachysyndactyly syndrome | Is a | True | Hereditary dysplasia of blood vessel | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets
FHIR