Status: current, Primitive. 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 | Active | Case insensitive | SNOMED CT core |
| 3701876015 | MTLE-HS - mesial temporal lobe epilepsy with hippocampal sclerosis | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3701877012 | Mesial temporal lobe epilepsy with hippocampal sclerosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 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 | Case sensitive | 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 | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Mesial temporal lobe epilepsy with hippocampal sclerosis | Is a | Disorder of cerebral cortex | true | Inferred relationship | Some | ||
| Mesial temporal lobe epilepsy with hippocampal sclerosis | Is a | Limbic disorder | true | Inferred relationship | Some | ||
| Mesial temporal lobe epilepsy with hippocampal sclerosis | Finding site | Hippocampal structure | true | Inferred relationship | Some | 1 | |
| Mesial temporal lobe epilepsy with hippocampal sclerosis | Associated morphology | Sclerosis | true | Inferred relationship | Some | 1 | |
| Mesial temporal lobe epilepsy with hippocampal sclerosis | Is a | Lesion of brain | true | Inferred relationship | Some | ||
| Mesial temporal lobe epilepsy with hippocampal sclerosis | Is a | Temporal lobe epilepsy | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Queensland allied health clinical finding reference set
Queensland allied health indicator for intervention reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR