Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4670002012 | AApoAIV (apolipoprotein A-IV) amyloidosis | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4670003019 | Apolipoprotein A-IV amyloidosis | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 4670004013 | Apolipoprotein A-IV amyloidosis (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5399568019 | A rare nonhereditary systemic amyloidosis characterized by slowly progressive renal dysfunction, increased serum creatinine, mostly normal urine analysis with no significant proteinuria and associated heart disease. Cardiac involvement presents as hypertrophic obstructive cardiomyopathy, left ventricular outflow tract obstruction, coronary artery disease and conduction system abnormalities. Histology reveals medullar amyloid deposits, renal tubular atrophy, interstitial fibrosis, and glomerular sclerosis. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5399569010 | A rare nonhereditary systemic amyloidosis characterised by slowly progressive renal dysfunction, increased serum creatinine, mostly normal urine analysis with no significant proteinuria and associated heart disease. Cardiac involvement presents as hypertrophic obstructive cardiomyopathy, left ventricular outflow tract obstruction, coronary artery disease and conduction system abnormalities. Histology reveals medullar amyloid deposits, renal tubular atrophy, interstitial fibrosis, and glomerular sclerosis. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Apolipoprotein A-IV amyloidosis | Is a | Renal disorders in systemic disease | true | Inferred relationship | Some | ||
| Apolipoprotein A-IV amyloidosis | Is a | Toxic nephropathy | true | Inferred relationship | Some | ||
| Apolipoprotein A-IV amyloidosis | Is a | Amyloid nephropathy | true | Inferred relationship | Some | ||
| Apolipoprotein A-IV amyloidosis | Is a | Systemic amyloidosis | true | Inferred relationship | Some | ||
| Apolipoprotein A-IV amyloidosis | Finding site | Kidney structure | true | Inferred relationship | Some | 1 | |
| Apolipoprotein A-IV amyloidosis | Associated morphology | Amyloid deposition | true | Inferred relationship | Some | 1 | |
| Apolipoprotein A-IV amyloidosis | Causative agent | Apolipoprotein A-IV (substance) | 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