Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3763690018 | Familial infantile myoclonus epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3763691019 | FIME - familial infantile myoclonic epilepsy | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3763692014 | Familial infantile myoclonic epilepsy | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3763693016 | Familial infantile myoclonic epilepsy (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3763694010 | A rare genetic infantile epilepsy syndrome disease with characteristics of neonatal to infancy onset myoclonic focal seizures occurring in various members of a family, associated in some with mild dysarthria, ataxia and borderline-to-moderate intellectual disability. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial infantile myoclonic epilepsy | est un(e) (attribut) | Myoclonic seizure | true | Inferred relationship | Some | ||
| Familial infantile myoclonic epilepsy | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Familial infantile myoclonic epilepsy | localisation d'une constatation (attribut) | structure du cerveau | true | Inferred relationship | Some | 1 | |
| Familial infantile myoclonic epilepsy | est un(e) (attribut) | Hereditary disorder of nervous system | true | Inferred relationship | Some | ||
| Familial infantile myoclonic epilepsy | survenue (attribut) | Infancy (qualifier value) | true | Inferred relationship | Some | 1 | |
| Familial infantile myoclonic epilepsy | est un(e) (attribut) | Familial disease | true | Inferred relationship | Some | ||
| Familial infantile myoclonic epilepsy | interprète (attribut) | Movement (observable entity) | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR