Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
492842013 | Deficiency of glyoxylate reductase | en | Synonym | Active | Case insensitive | SNOMED CT core |
492843015 | Deficiency of glycerate dehydrogenase | en | Synonym | Active | Case insensitive | SNOMED CT core |
492844014 | Oxalosis type II | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
492845010 | Primary hyperoxaluria type II | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
68304013 | Primary hyperoxaluria, type II | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
68305014 | Glyoxylate reductase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
68306010 | Glyceric dehydrogenase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
68307018 | L-glyceric aciduria | en | Synonym | Active | Case sensitive | SNOMED CT core |
68308011 | Glycerate dehydrogenase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
777685010 | Primary hyperoxaluria, type II (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Primary hyperoxaluria, type II | Is a | Primary hyperoxaluria | true | Inferred relationship | Some | ||
Primary hyperoxaluria, type II | Finding site | Kidney structure | true | Inferred relationship | Some | 2 | |
Primary hyperoxaluria, type II | Occurrence | Congenital | 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
Australian dialect reference set
Problem/Diagnosis reference set