Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3655822015 | Familial TAAD (thoracic aortic aneurysm aortic dissection) | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 3655823013 | Familial thoracic aortic aneurysm and aortic dissection | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 3655824019 | Familial thoracic aortic aneurysm and aortic dissection (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 3655829012 | A rare genetic vascular disease characterized by the familial occurrence of thoracic aortic aneurysm, dissection or dilatation affecting one or more aortic segments (aortic root, ascending aorta, arch or descending aorta) in the absence of any other associated disease. Depending on the size, location and progression rate of dilatation/dissection, patients may be asymptomatic or may present dyspnea, cough, jaw, neck, chest or back pain, head, neck or upper limb edema, difficulty swallowing, voice hoarseness, pale skin, faint pulse and/or numbness/tingling in limbs. Patients have increased risk of presenting life threatening aortic rupture. | en | Definition | Active | Case sensitive | SNOMED CT core |
| 3655830019 | A rare genetic vascular disease characterised by the familial occurrence of thoracic aortic aneurysm, dissection or dilatation affecting one or more aortic segments (aortic root, ascending aorta, arch or descending aorta) in the absence of any other associated disease. Depending on the size, location and progression rate of dilatation/dissection, patients may be asymptomatic or may present dyspnoea, cough, jaw, neck, chest or back pain, head, neck or upper limb oedema, difficulty swallowing, voice hoarseness, pale skin, faint pulse and/or numbness/tingling in limbs. Patients have increased risk of presenting life threatening aortic rupture. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial thoracic aortic aneurysm and aortic dissection | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
| Familial thoracic aortic aneurysm and aortic dissection | Associated morphology | Dilatation | true | Inferred relationship | Some | 1 | |
| Familial thoracic aortic aneurysm and aortic dissection | Is a | Developmental hereditary disorder | true | Inferred relationship | Some | ||
| Familial thoracic aortic aneurysm and aortic dissection | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Familial thoracic aortic aneurysm and aortic dissection | Is a | Congenital dilatation of aorta | true | Inferred relationship | Some | ||
| Familial thoracic aortic aneurysm and aortic dissection | Is a | Familial disease | true | Inferred relationship | Some | ||
| Familial thoracic aortic aneurysm and aortic dissection | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| Familial thoracic aortic aneurysm and aortic dissection | Is a | Congenital anomaly of thorax | true | Inferred relationship | Some | ||
| Familial thoracic aortic aneurysm and aortic dissection | Is a | Ectasia of thoracic aorta | true | Inferred relationship | Some | ||
| Familial thoracic aortic aneurysm and aortic dissection | Associated morphology | Congenital dilatation | false | Inferred relationship | Some | 1 | |
| Familial thoracic aortic aneurysm and aortic dissection | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Familial thoracic aortic aneurysm and aortic dissection | Finding site | Thoracic aorta structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set
FHIR