Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3701875016 | Mesial temporal lobe epilepsy with hippocampal sclerosis | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3701876015 | MTLE-HS - mesial temporal lobe epilepsy with hippocampal sclerosis | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3701877012 | Mesial temporal lobe epilepsy with hippocampal sclerosis (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 769591000241111 | epilepsie du lobe mésio-temporal avec sclérose de l'hippocampe (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 970231000172114 | MTLE-HS - mesial temporal lobe epilepsy with hippocampal sclerosis | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 978411000172115 | epilepsie du lobe mésio-temporal avec sclérose de l'hippocampe | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
| 3701878019 | A rare epilepsy syndrome defined by seizures originating in limbic areas of the mesial temporal lobe, particularly in the hippocampus, amygdala, and in the parahippocampal gyrus and its connections, and hippocampal sclerosis, usually unilateral or asymmetric. It is frequently associated with an initial precipitating event, such as febrile seizures, hypoxia, intracranial infection or head trauma, most often occurring in the first five years of life, followed by a latent period without seizures. Typical seizures consist of a characteristic aura that is frequently a rising epigastric sensation associated with emotional disturbances, illusions, and autonomic symptoms (widened pupils, palpitations), progressive impairment of consciousness, oro-alimentary automatisms (lip smacking, chewing, licking, tooth grinding), behavioural arrest, head deviation, dystonic postures, hand and verbal automatisms. Seizures are followed by postictal dysfunction. Initially, seizures are easily controlled with antiepileptic drugs, later they frequently become refractory and associated with progressive behavioural changes and memory deficits. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3701879010 | A rare epilepsy syndrome defined by seizures originating in limbic areas of the mesial temporal lobe, particularly in the hippocampus, amygdala, and in the parahippocampal gyrus and its connections, and hippocampal sclerosis, usually unilateral or asymmetric. It is frequently associated with an initial precipitating event, such as febrile seizures, hypoxia, intracranial infection or head trauma, most often occurring in the first five years of life, followed by a latent period without seizures. Typical seizures consist of a characteristic aura that is frequently a rising epigastric sensation associated with emotional disturbances, illusions, and autonomic symptoms (widened pupils, palpitations), progressive impairment of consciousness, oro-alimentary automatisms (lip smacking, chewing, licking, tooth grinding), behavioral arrest, head deviation, dystonic postures, hand and verbal automatisms. Seizures are followed by postictal dysfunction. Initially, seizures are easily controlled with antiepileptic drugs, later they frequently become refractory and associated with progressive behavioral changes and memory deficits. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Mesial temporal lobe epilepsy with hippocampal sclerosis | est un(e) (attribut) | Disorder of cerebral cortex | true | Inferred relationship | Some | ||
| Mesial temporal lobe epilepsy with hippocampal sclerosis | est un(e) (attribut) | Limbic disorder (disorder) | true | Inferred relationship | Some | ||
| Mesial temporal lobe epilepsy with hippocampal sclerosis | localisation d'une constatation (attribut) | Hippocampal structure | true | Inferred relationship | Some | 1 | |
| Mesial temporal lobe epilepsy with hippocampal sclerosis | morphologie associée (attribut) | sclérose (anomalie morphologique) | true | Inferred relationship | Some | 1 | |
| Mesial temporal lobe epilepsy with hippocampal sclerosis | est un(e) (attribut) | lésion cérébrale | true | Inferred relationship | Some | ||
| Mesial temporal lobe epilepsy with hippocampal sclerosis | est un(e) (attribut) | Temporal lobe epilepsy | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR