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Biological and Environmental Research Ontology
Last uploaded:
December 23, 2022
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| Id | http://purl.obolibrary.org/obo/NCIT_C84816
http://purl.obolibrary.org/obo/NCIT_C84816
|
|---|---|
| Preferred Name | Lennox-Gastaut Syndrome |
| Definitions |
A syndrome characterized by frequent episodes of epilepsy during childhood. The epileptic episodes may be tonic, atonic, myoclonic, or absence seizures. It may be accompanied by mental retardation and behavioral problems.
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | A syndrome characterized by frequent episodes of epilepsy during childhood. The epileptic episodes may be tonic, atonic, myoclonic, or absence seizures. It may be accompanied by mental retardation and behavioral problems. |
|---|---|
| label |
Lennox-Gastaut Syndrome
|
| prefLabel |
Lennox-Gastaut Syndrome
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| in_subset | |
| Preferred_Name |
Lennox-Gastaut Syndrome
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| Maps_To |
Lennox-Gastaut syndrome
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| UMLS_CUI |
C0238111
|
| prefixIRI |
NCIT:C84816
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| Contributing_Source |
Cellosaurus
MedDRA
NICHD
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| subClassOf | |
| code |
C84816
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| type | |
| ALT_DEFINITION |
A severe form of childhood epilepsy that is characterized by frequent seizures of multiple types, a distinct electroencephalogram pattern consisting of slow spike-waves between seizures, behavioral disturbances, and cognitive dysfunction.
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| Semantic_Type |
Disease or Syndrome
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