Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2010. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2869027015 | Glucose transporter protein type 1 deficiency syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 2872335013 | Glucose transporter protein type 1 deficiency syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 1642921000000110 | GLUT1 (glucose transporter protein type 1) deficiency syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT United Kingdom Edition module |
| 1650271000000119 | De Vivo disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT United Kingdom Edition module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Glucose transporter protein type 1 deficiency syndrome | Is a | Metabolic encephalopathy | true | Inferred relationship | Existential restriction modifier | ||
| Glucose transporter protein type 1 deficiency syndrome | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Glucose transporter protein type 1 deficiency syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Glucose transporter protein type 1 deficiency syndrome | Finding site | Brain structure | true | Inferred relationship | Existential restriction modifier | 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 | Existential restriction modifier | 2 |
This concept is not in any reference sets
FHIR