Application Version: 4.0.6.10
Content Version: 2024.07.12
Release Notes [PDF288KB]
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Code System Concept
Code System Concept Code | 36803009 |
Code System Concept Name | Idiopathic generalized epilepsy (disorder) |
Code System Preferred Concept Name | Idiopathic generalized epilepsy (disorder) |
Concept Status | Published |
Concept Status Date | 09/01/2024 |
Code System Name | SNOMED-CT |
Concept Details
Code System Code | PH_SNOMED-CT |
Code System OID | 2.16.840.1.113883.6.96 |
HL7 Table 0396 Code | SCT |
Superseded By Concept | |
SDO Concept Status | Active |
SDO Concept Status Date | 01/31/2002 |
SDO Date Created | 01/31/2002 |
SDO Date Revised | 01/31/2002 |
Description | A distinct sub-group of genetic generalized epilepsy that includes only four epilepsy syndromes: childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy, and epilepsy with generalized tonic-clonic seizures alone. |
Sequence |
Extended Properties
No extended properties.
Concept Alternate Designations
SDO Designation ID | Concept Designation Description | Status | Designation Type | PHIN Preferred Term Flag | Code Flag |
---|---|---|---|---|---|
1216513011 | Primary generalised epilepsy | Active | Synonym | false | false |
1218003019 | Primary generalized epilepsy | Active | Synonym | false | false |
486556017 | Idiopathic generalised epilepsy | Active | Synonym | false | false |
5160677019 | IGE - idiopathic generalized epilepsy | Active | Synonym | false | false |
5160679016 | IGE - idiopathic generalised epilepsy | Active | Synonym | false | false |
61389013 | Idiopathic generalized epilepsy | Active | Synonym | false | false |
- Page last reviewed:June 20, 2024
- Page last updated:June 20, 2024
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