Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3736359010 | Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 3736360017 | KCNQ2-related neonatal epileptic encephalopathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3736361018 | KCNQ2-NEE - potassium voltage-gated channel subfamily Q member 2-related neonatal epileptic encephalopathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3736362013 | KCNQ2-related epileptic encephalopathy | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 3736363015 | Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy | Occurrence | Neonatal | true | Inferred relationship | Existential restriction modifier | 1 | |
| Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy | Finding site | Structure of cerebrum | true | Inferred relationship | Existential restriction modifier | 1 | |
| Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy | Is a | Epileptic encephalopathy | true | Inferred relationship | Existential restriction modifier | ||
| Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Existential restriction modifier | ||
| Potassium voltage-gated channel subfamily Q member 2 related epileptic encephalopathy | Is a | Neonatal disorder | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR