Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3326212015 | Hyperuricemia, anemia, renal failure syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3326213013 | Hyperuricemia, anemia, renal failure syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3326214019 | Hyperuricaemia, anaemia, renal failure syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3326215018 | Familial juvenile hyperuricemic nephropathy type 2 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3326216017 | Familial juvenile hyperuricaemic nephropathy type 2 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3326217014 | Renin associated familial juvenile hyperuricemic nephropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3326218016 | Renin associated familial juvenile hyperuricaemic nephropathy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3326219012 | A rare autosomal dominantly inherited disease of childhood characterized by hypoproliferative anemia, hyperuricemia and slowly progressing kidney failure due to dysregulation of the renin-angiotensin system. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3326220018 | A rare autosomal dominantly inherited disease of childhood characterised by hypoproliferative anaemia, hyperuricaemia and slowly progressing kidney failure due to dysregulation of the renin-angiotensin system. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hyperuricemia, anemia, renal failure syndrome (disorder) | localisation d'une constatation (attribut) | structure d'un rein | true | Inferred relationship | Some | 2 | |
| Hyperuricemia, anemia, renal failure syndrome (disorder) | Causative agent | Urate | true | Inferred relationship | Some | 2 | |
| Hyperuricemia, anemia, renal failure syndrome (disorder) | est un(e) (attribut) | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Hyperuricemia, anemia, renal failure syndrome (disorder) | est un(e) (attribut) | hyperuricémie (trouble) | true | Inferred relationship | Some | ||
| Hyperuricemia, anemia, renal failure syndrome (disorder) | est un(e) (attribut) | Renal tubular disorder | true | Inferred relationship | Some | ||
| Hyperuricemia, anemia, renal failure syndrome (disorder) | est un(e) (attribut) | Urate nephropathy | true | Inferred relationship | Some | ||
| Hyperuricemia, anemia, renal failure syndrome (disorder) | est un(e) (attribut) | Hereditary nephropathy (disorder) | true | Inferred relationship | Some | ||
| Hyperuricemia, anemia, renal failure syndrome (disorder) | localisation d'une constatation (attribut) | Renal tubule structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Canada English language reference set (foundation metadata concept)
FHIR