Preferred Name | Myoclonic Epilepsy, Juvenile | |
Synonyms |
Epilepsy, Adolescent Myoclonic Adolescent Myoclonic Epilepsy Juvenile Myoclonic Epilepsy of Janz Epilepsy, Myoclonic Juvenile Epilepsy, Juvenile Myoclonic Myoclonic Epilepsy, Juvenile, 1 Myoclonic Epilepsy, Adolescent Petit Mal, Impulsive, Janz Impulsive Petit Mal Epilepsy Janz Juvenile Myoclonic Epilepsy JME (Juvenile Myoclonic Epilepsy) JMEs (Juvenile Myoclonic Epilepsy) Juvenile Myoclonic Epilepsy Myoclonic Juvenile Epilepsy Petit Mal, Impulsive Impulsive Petit Mal, Janz Janz Syndrome Juvenile Epilepsy, Myoclonic Epilepsy, Myoclonic, Juvenile Janz Impulsive Petit Mal |
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Definitions |
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) |
|
ID |
http://purl.bioontology.org/ontology/MESH/D020190 |
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altLabel |
Epilepsy, Adolescent Myoclonic Adolescent Myoclonic Epilepsy Juvenile Myoclonic Epilepsy of Janz Epilepsy, Myoclonic Juvenile Epilepsy, Juvenile Myoclonic Myoclonic Epilepsy, Juvenile, 1 Myoclonic Epilepsy, Adolescent Petit Mal, Impulsive, Janz Impulsive Petit Mal Epilepsy Janz Juvenile Myoclonic Epilepsy JME (Juvenile Myoclonic Epilepsy) JMEs (Juvenile Myoclonic Epilepsy) Juvenile Myoclonic Epilepsy Myoclonic Juvenile Epilepsy Petit Mal, Impulsive Impulsive Petit Mal, Janz Janz Syndrome Juvenile Epilepsy, Myoclonic Epilepsy, Myoclonic, Juvenile Janz Impulsive Petit Mal |
|
AQL |
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI |
|
cui |
C0270853 |
|
DC |
1 |
|
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) |
|
DX |
20000101 |
|
HN |
2000 |
|
Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000178 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000469 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000209 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000652 |
|
Machine permutation |
2000 |
|
MDA |
19991103 |
|
MMR |
20181010 |
|
MN |
C10.228.140.490.375.130.670 C10.228.140.490.493.063.670 |
|
notation |
D020190 |
|
prefLabel |
Myoclonic Epilepsy, Juvenile |
|
TERMUI |
T369662 T369663 T358258 T369665 T769545 T369666 T841801 T769546 T369667 T369670 T369672 T369669 T369668 T812251 T369671 T369664 |
|
TH |
OMIM (2013) NLM (2000) GHR (2014) NLM (2011) ORD (2010) |
|
tui |
T047 |
|
subClassOf |