Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2475895017 | Deficiency of arginase | en | Synonym | Active | Case insensitive | SNOMED CT core |
39458015 | Arginase deficiency | en | Synonym | Active | Case insensitive | SNOMED CT core |
39459011 | Argininemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
39460018 | Hyperargininemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
39461019 | ARGI deficiency | en | Synonym | Active | Case sensitive | SNOMED CT core |
481635014 | Argininaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
481636010 | Hyperargininaemia | en | Synonym | Active | Case insensitive | SNOMED CT core |
753030010 | Arginase deficiency (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Arginase deficiency | Is a | Inherited metabolic disorder of nervous system | true | Inferred relationship | Some | ||
Arginase deficiency | Is a | Disorder of the urea cycle metabolism | true | Inferred relationship | Some | ||
Arginase deficiency | Is a | Enzymopathy | false | Inferred relationship | Some | ||
Arginase deficiency | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Arginase deficiency | Is a | Specific enzyme deficiency | true | Inferred relationship | Some | ||
Arginase deficiency | Finding site | Structure of nervous system | true | Inferred relationship | Some | 2 | |
Arginase deficiency | 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
Problem/Diagnosis reference set