Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
345270013 | Benign neonatal epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
345271012 | BFNC - Benign familial neonatal convulsions | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
345272017 | Benign neonatal familial convulsions | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
618214010 | Benign neonatal familial convulsions (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
214551000172117 | épilepsie néonatale familiale bénigne | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Benign neonatal familial convulsions | Is a | Idiopathic generalized epilepsy | false | Inferred relationship | Some | ||
Benign neonatal familial convulsions | Is a | Benign neonatal convulsions | true | Inferred relationship | Some | ||
Benign neonatal familial convulsions | Occurrence | Neonatal | true | Inferred relationship | Some | 1 | |
Benign neonatal familial convulsions | Finding site | Cerebrum | false | Inferred relationship | Some | 2 | |
Benign neonatal familial convulsions | Occurrence | Perinatal state | false | Inferred relationship | Some | ||
Benign neonatal familial convulsions | Occurrence | période périnatale | false | Inferred relationship | Some | ||
Benign neonatal familial convulsions | Has definitional manifestation | Seizure | false | Inferred relationship | Some | ||
Benign neonatal familial convulsions | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Benign neonatal familial convulsions | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
Benign neonatal familial convulsions | Finding site | Cerebrum | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets