Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 482140017 | Cardiovascular system hereditary disorder | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 754780015 | Cardiovascular system hereditary disorder (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Cardiovascular system hereditary disorder | est un(e) (attribut) | Hereditary disorder by system | true | Inferred relationship | Some | ||
| Cardiovascular system hereditary disorder | est un(e) (attribut) | Disorder of cardiovascular system (disorder) | true | Inferred relationship | Some | ||
| Cardiovascular system hereditary disorder | localisation d'une constatation (attribut) | Structure of cardiovascular system (body structure) | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Familial bicuspid aortic valve (disorder) | est un(e) (attribut) | True | Cardiovascular system hereditary disorder | Inferred relationship | Some | |
| Vasculitis due to adenosine deaminase 2 deficiency | est un(e) (attribut) | True | Cardiovascular system hereditary disorder | Inferred relationship | Some | |
| Sinoatrial node dysfunction and deafness | est un(e) (attribut) | True | Cardiovascular system hereditary disorder | Inferred relationship | Some | |
| syndrome d'extrasystoles, petite taille, hyperpigmentation, microcéphalie | est un(e) (attribut) | True | Cardiovascular system hereditary disorder | Inferred relationship | Some |
This concept is not in any reference sets
FHIR