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EpilepsyOntology
Last uploaded:
November 8, 2021
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| Id | http://purl.obolibrary.org/obo/DOID_0060172
http://purl.obolibrary.org/obo/DOID_0060172
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|---|---|
| Preferred Name | juvenile absence epilepsy |
| Definitions |
An adolescence-adult electroclinical syndrome statring between the age of ten to 17 years characterized by the occurrence of typical absence seizures.
JA:Epilepsy Genetics Kiel
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| label |
juvenile absence epilepsy
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|---|---|
| comment |
JA:Epilepsy Genetics Kiel
|
| prefLabel |
juvenile absence epilepsy
|
| notation |
DOID:0060172
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| creation_date |
2011-11-08T10:42:18Z
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| id |
DOID:0060172
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| fromEPILONT |
true
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| created_by |
lschriml
|
| has_obo_namespace |
disease_ontology
|
| fromEpSO | |
| see also | |
| 文本定义 |
An adolescence-adult electroclinical syndrome statring between the age of ten to 17 years characterized by the occurrence of typical absence seizures.
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| subClassOf | |
| imported from | |
| hasDefinition |
This genetic/idiopathic generalized epilepsy is characterized by absence seizures that are not very frequent in an otherwise normal adolescent or adult. Generalized tonic-clonic seizures typically also occur. With absence seizures in a child aged between 8 and 12 years, a diagnosis of juvenile absence epilepsy or childhood absence epilepsy depends on the frequency of the absence seizures.
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| fromILAE |
true
|
| type |
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