loading...| Preferred Name | Dravet Syndrome | |
| Synonyms |
Severe Myoclonic Epilepsy of Infancy Dravet Syndrome SMEI |
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| Definitions |
A severe form of epilepsy that presents in early childhood and is characterized by frequent, prolonged febrile or myoclonic seizures that may progress to status epilepticus and poor development of language, motor, and socialization skills. |
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| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116573 |
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| ALT_DEFINITION |
A severe form of epilepsy that presents in early childhood and is characterized by frequent, prolonged febrile or myoclonic seizures that may progress to status epilepticus and poor development of language, motor, and socialization skills. |
|
| code |
C116573 |
|
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C192842 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C165258 |
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| Contributing_Source |
Cellosaurus MedDRA NICHD |
|
| DEFINITION |
A severe form of epilepsy that presents in early childhood and is characterized by frequent, prolonged febrile or myoclonic seizures that may progress to status epilepticus and poor development of language, motor, and socialization skills. |
|
| FULL_SYN |
Severe Myoclonic Epilepsy of Infancy Dravet Syndrome SMEI |
|
| label |
Dravet Syndrome |
|
| Maps_To |
Dravet syndrome |
|
| Preferred_Name |
Dravet Syndrome |
|
| prefixIRI |
Thesaurus:C116573 |
|
| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0751122 |
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| subClassOf |