Status: current, Defined. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
125653016 | Familial renal iminoglycinuria | en | Synonym | Active | Case insensitive | SNOMED CT core |
816286010 | Familial renal iminoglycinuria (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial renal iminoglycinuria | Is a | Hereditary disorder of the urinary system | false | Inferred relationship | Some | ||
Familial renal iminoglycinuria | Is a | Inborn error of metabolism | true | Inferred relationship | Some | ||
Familial renal iminoglycinuria | Is a | Familial disease | true | Inferred relationship | Some | ||
Familial renal iminoglycinuria | Is a | Iminoglycinuria | true | Inferred relationship | Some | ||
Familial renal iminoglycinuria | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Familial renal iminoglycinuria | Is a | Hereditary nephropathy | true | Inferred relationship | Some | ||
Familial renal iminoglycinuria | Finding site | Kidney structure | true | Inferred relationship | Some | 2 | |
Familial renal iminoglycinuria | 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