Status: current, Not 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 |
| 67513013 | Fanconi syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 777141012 | Fanconi syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5959381000172112 | syndrome de Fanconi | fr | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| 5240311000172114 | Fanconi-syndroom | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | Belgian module (core metadata concept) |
| 8546631000172112 | syndroom van Fanconi | nl | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | Belgian module (core metadata concept) |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Fanconi syndrome | Is a | Renal tubular disorder | true | Inferred relationship | Some | ||
| Fanconi syndrome | Is a | Congenital anomaly of trunk | false | Inferred relationship | Some | ||
| Fanconi syndrome | Is a | Amino acid transport disorder | true | Inferred relationship | Some | ||
| Fanconi syndrome | Is a | Hereditary disorder of the urinary system | false | Inferred relationship | Some | ||
| Fanconi syndrome | Associated morphology | Inflammation | false | Inferred relationship | Some | ||
| Fanconi syndrome | Occurrence | Congenital | false | Inferred relationship | Some | ||
| Fanconi syndrome | Finding site | Structure of interstitial tissue of kidney | false | Inferred relationship | Some | ||
| Fanconi syndrome | Finding site | Renal tubule structure (body structure) | true | Inferred relationship | Some | 1 | |
| Fanconi syndrome | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
| Fanconi syndrome | Is a | Metabolic renal disease | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Fanconi-de Toni-Debre syndrome | Is a | False | Fanconi syndrome | Inferred relationship | Some | |
| Acquired Fanconi syndrome | Is a | True | Fanconi syndrome | Inferred relationship | Some | |
| Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome (disorder) | Is a | True | Fanconi syndrome | Inferred relationship | Some |
Reference Sets
Belgian GP subset (foundation metadata concept)
Belgian subset for medical problems in patient health records
FHIR