Status: current, Primitive. Date: 30-Sep 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5099849014 | Benign familial infantile epilepsy (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 5099850014 | BFIE - benign familial infantile epilepsy | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 5099851013 | BFIS - benign familial infantile seizures | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 5099852018 | Benign familial infantile epilepsy | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 5099853011 | Benign familial infantile convulsions | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 5099854017 | A genetic epileptic syndrome characterized by the occurrence of afebrile repeated seizures in healthy infants, between the third and eighth month of life with clusters (8-10 a day) of repeated and brief episodes (2-5 minutes) over a few days. They are usually focal but can sometimes become generalized. A family history of the same epilepsy is a constant finding. The disease is genetically heterogeneous, in the majority of cases, mutations in the proline-rich transmembrane protein 2 (PRRT2) gene located at 16p11.2 have been found. Mutations have also been found in the SCN2A gene (2q24.3) encoding the brain sodium channel NaV1.2 and rarely in the KCNQ2 (20q13.33) and KCNQ3 (8q24) genes both encoding potassium channels. Additionally, three other chromosomal loci have been identified that are mapped to chromosome 19q, 16p and 1p. Transmitted as an autosomal dominant trait with incomplete penetrance. | en | Definition | Active | Case sensitive | SNOMED CT core |
| 5099855016 | A genetic epileptic syndrome characterised by the occurrence of afebrile repeated seizures in healthy infants, between the third and eighth month of life with clusters (8-10 a day) of repeated and brief episodes (2-5 minutes) over a few days. They are usually focal but can sometimes become generalised. A family history of the same epilepsy is a constant finding. The disease is genetically heterogeneous, in the majority of cases, mutations in the proline-rich transmembrane protein 2 (PRRT2) gene located at 16p11.2 have been found. Mutations have also been found in the SCN2A gene (2q24.3) encoding the brain sodium channel NaV1.2 and rarely in the KCNQ2 (20q13.33) and KCNQ3 (8q24) genes both encoding potassium channels. Additionally, three other chromosomal loci have been identified that are mapped to chromosome 19q, 16p and 1p. Transmitted as an autosomal dominant trait with incomplete penetrance. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Benign familial infantile epilepsy | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Benign familial infantile epilepsy | Is a | Partial seizure | true | Inferred relationship | Some | ||
| Benign familial infantile epilepsy | Is a | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Benign familial infantile epilepsy | Is a | Epilepsy | true | Inferred relationship | Some | ||
| Benign familial infantile epilepsy | Occurrence | Infancy | true | Inferred relationship | Some | 1 | |
| Benign familial infantile epilepsy | Finding site | Structure of cerebrum | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR