Status: current, Primitive. Date: 31-Jul 2010. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2869027015 | Glucose transporter protein type 1 deficiency syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
2872335013 | Glucose transporter protein type 1 deficiency syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Glucose transporter protein type 1 deficiency syndrome | Is a | Metabolic encephalopathy | true | Inferred relationship | Some | ||
Glucose transporter protein type 1 deficiency syndrome | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Glucose transporter protein type 1 deficiency syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Glucose transporter protein type 1 deficiency syndrome | Finding site | Brain structure | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Epilepsy due to glucose transporter protein type 1 deficiency syndrome | Due to | True | Glucose transporter protein type 1 deficiency syndrome | Inferred relationship | Some | 2 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set