National Drug File - Reference Terminology - Myoclonic Epilepsy, Juvenile [Disease/Finding] - Classes | NCBO BioPortal

National Drug File - Reference Terminology

Last uploaded: July 6, 2018

Id	http://purl.bioontology.org/ontology/NDFRT/N0000004029 http://purl.bioontology.org/ontology/NDFRT/N0000004029
Preferred Name	Myoclonic Epilepsy, Juvenile [Disease/Finding]
Synonyms	Adolescent Myoclonic Epilepsy Juvenile Myoclonic Epilepsy of Janz Epilepsy, Myoclonic Juvenile Myoclonic Epilepsy, Juvenile, 1 Myoclonic Epilepsy, Adolescent Petit Mal, Impulsive, Janz Impulsive Petit Mal Epilepsy Janz Juvenile Myoclonic Epilepsy JME (Juvenile Myoclonic Epilepsy) Juvenile Myoclonic Epilepsy Petit Mal, Impulsive Impulsive Petit Mal, Janz Janz Syndrome Epilepsy, Myoclonic, Juvenile Myoclonic Epilepsy, Juvenile Janz Impulsive Petit Mal See more See less
Type	http://www.w3.org/2002/07/owl#Class

altLabel	Adolescent Myoclonic Epilepsy Juvenile Myoclonic Epilepsy of Janz Epilepsy, Myoclonic Juvenile Myoclonic Epilepsy, Juvenile, 1 Myoclonic Epilepsy, Adolescent Petit Mal, Impulsive, Janz Impulsive Petit Mal Epilepsy Janz Juvenile Myoclonic Epilepsy JME (Juvenile Myoclonic Epilepsy) Juvenile Myoclonic Epilepsy Petit Mal, Impulsive Impulsive Petit Mal, Janz Janz Syndrome Epilepsy, Myoclonic, Juvenile Myoclonic Epilepsy, Juvenile Janz Impulsive Petit Mal See more See less
prefLabel	Myoclonic Epilepsy, Juvenile [Disease/Finding]
MESH DEFINITION	A disorder characterized by the onset of myoclonus in adolescence, a marked increase in the incidence of absence seizures (see EPILEPSY, ABSENCE), and generalized major motor seizures (see EPILEPSY, TONIC-CLONIC). The myoclonic episodes tend to occur shortly after awakening. Seizures tend to be aggravated by sleep deprivation and alcohol consumption. Hereditary and sporadic forms have been identified. (From Adams et al., Principles of Neurology, 6th ed, p323)
MESH DUI	D020190
MESH UI	M0328258
MeSH name	Myoclonic Epilepsy, Juvenile
type	http://www.w3.org/2002/07/owl#Class
tui	T047
SNOMED CID	6204001
May be treated by	http://purl.bioontology.org/ontology/NDFRT/N0000148644 http://purl.bioontology.org/ontology/NDFRT/N0000164660 http://purl.bioontology.org/ontology/NDFRT/N0000192495 http://purl.bioontology.org/ontology/NDFRT/N0000162315 http://purl.bioontology.org/ontology/NDFRT/N0000177410 http://purl.bioontology.org/ontology/NDFRT/N0000177411 http://purl.bioontology.org/ontology/NDFRT/N0000178212 http://purl.bioontology.org/ontology/NDFRT/N0000192496 http://purl.bioontology.org/ontology/NDFRT/N0000192494 http://purl.bioontology.org/ontology/NDFRT/N0000162314 http://purl.bioontology.org/ontology/NDFRT/N0000178535 http://purl.bioontology.org/ontology/NDFRT/N0000162313 http://purl.bioontology.org/ontology/NDFRT/N0000192085 http://purl.bioontology.org/ontology/NDFRT/N0000192497 See more See less
notation	N0000004029
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
NUI	N0000004029
cui	C0270853
NDFRT kind	DISEASE_KIND
subClassOf	http://purl.bioontology.org/ontology/NDFRT/N0000001130

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