Status: current, Defined. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 482140017 | Cardiovascular system hereditary disorder | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 754780015 | Cardiovascular system hereditary disorder (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Cardiovascular system hereditary disorder | Is a | Hereditary disorder by system | true | Inferred relationship | Some | ||
| Cardiovascular system hereditary disorder | Is a | Cardiovascular disease | true | Inferred relationship | Some | ||
| Cardiovascular system hereditary disorder | Finding site | Structure of cardiovascular system | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Hypertension due to gain-of-function mutation in mineralocorticoid receptor | Is a | True | Cardiovascular system hereditary disorder | Inferred relationship | Some | |
| Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation | Is a | True | Cardiovascular system hereditary disorder | Inferred relationship | Some | |
| Familial bicuspid aortic valve | Is a | True | Cardiovascular system hereditary disorder | Inferred relationship | Some | |
| Vasculitis due to adenosine deaminase 2 deficiency | Is a | True | Cardiovascular system hereditary disorder | Inferred relationship | Some | |
| Sinoatrial node dysfunction and deafness | Is a | True | Cardiovascular system hereditary disorder | Inferred relationship | Some | |
| Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome | Is a | True | Cardiovascular system hereditary disorder | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set
FHIR