Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
139496018 | Iminoglycinuria | en | Synonym | Active | Case insensitive | SNOMED CT core |
825899010 | Iminoglycinuria (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Iminoglycinuria | Is a | Metabolic renal disease | true | Inferred relationship | Some | ||
Iminoglycinuria | Is a | Congenital anomaly of trunk | false | Inferred relationship | Some | ||
Iminoglycinuria | Is a | Specific renal tubule transport defect | true | Inferred relationship | Some | ||
Iminoglycinuria | Is a | Amino acid transport disorder | true | Inferred relationship | Some | ||
Iminoglycinuria | Is a | Hereditary disorder of the urinary system | false | Inferred relationship | Some | ||
Iminoglycinuria | Occurrence | Congenital | false | Inferred relationship | Some | ||
Iminoglycinuria | Finding site | Kidney structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Neonatal iminoglycinuria | Is a | True | Iminoglycinuria | Inferred relationship | Some | |
Familial renal iminoglycinuria | Is a | True | Iminoglycinuria | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set