Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5099852018 | Benign familial infantile epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5099853011 | Benign familial infantile convulsions | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5380926016 | Self-limited familial infantile epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5380927013 | Self-limited familial infantile epilepsy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5380928015 | SeLFIE - self-limited familial infantile epilepsy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400303016 | Benign familial infantile epilepsy (BFIE) is a genetic epileptic syndrome characterized by the occurrence of afebrile repeated seizures in healthy infants, between the third and eighth month of life. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400304010 | Benign familial infantile epilepsy (BFIE) is a genetic epileptic syndrome characterised by the occurrence of afebrile repeated seizures in healthy infants, between the third and eighth month of life. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Self-limited familial infantile epilepsy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Self-limited familial infantile epilepsy | Is a | Focal onset epileptic seizure | false | Inferred relationship | Some | ||
| Self-limited familial infantile epilepsy | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Self-limited familial infantile epilepsy | Is a | Epilepsy | false | Inferred relationship | Some | ||
| Self-limited familial infantile epilepsy | Occurrence | Infancy | true | Inferred relationship | Some | 1 | |
| Self-limited familial infantile epilepsy | Finding site | Cerebrum | false | Inferred relationship | Some | 1 | |
| Self-limited familial infantile epilepsy | Is a | Self-limited infantile epilepsy (disorder) | true | Inferred relationship | Some | ||
| Self-limited familial infantile epilepsy | Finding site | Brain structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR