Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3303311010 | Transthyretin related familial amyloid cardiomyopathy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303312015 | Transthyretin related familial amyloid cardiomyopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303313013 | Transthyretin amyloid cardiopathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3303314019 | ATTRV122I amyloidosis | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5423500013 | A rare hereditary Transthyretin (TTR)-related systemic amyloidosis (ATTR) with predominant cardiac involvement resulting from myocardial infiltration of abnormal amyloid protein. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Associated morphology | Amyloid deposition | true | Inferred relationship | Some | 1 | |
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Is a | Autosomal dominant hereditary disorder | false | Inferred relationship | Some | ||
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Is a | Familial restrictive cardiomyopathy | true | Inferred relationship | Some | ||
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Is a | Familial non-neuropathic amyloidosis | false | Inferred relationship | Some | ||
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Finding site | Myocardium structure | false | Inferred relationship | Some | 2 | |
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Is a | Hereditary amyloidosis (disorder) | false | Inferred relationship | Some | ||
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Is a | Myocardial degeneration | false | Inferred relationship | Some | ||
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Finding site | Myocardium structure | true | Inferred relationship | Some | 1 | |
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Causative agent | Prealbumin | true | Inferred relationship | Some | 1 | |
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Is a | Infiltrative cardiomyopathy | true | Inferred relationship | Some | ||
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Is a | Cardiac familial non-neuropathic amyloidosis | true | Inferred relationship | Some | ||
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Is a | Hereditary transthyretin related amyloidosis (disorder) | true | Inferred relationship | Some | ||
| Transthyretin related familial amyloid cardiomyopathy (disorder) | Occurrence | Adulthood | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR