About: myoclonic epilepsy

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

medical condition

Attributes	Values
rdf:type	Item
owl:sameAs	myoclonic epilepsy
description	medical condition (en) Krankheit (de) malattia (it) медичний стан (uk)
health specialty	wds:Q11883686-44B058F7-074C-4207-8B46-12B924EAAC89
drug or therapy used for treatment	wds:Q11883686-73E896A5-2595-4AAA-9C32-00B36B7EF7DA
symptoms and signs	wds:Q11883686-833DBC49-CF0A-478F-8DA7-D93F6A90B0D8
health specialty	neurology
drug or therapy used for treatment	clonazepam
symptoms and signs	myoclonus
rdfs:label	myoclonic epilepsy (en) Myoklonusepilepsia (fi) mioklonična epilepsija (sl) myoklon epilepsi (nn) ysgytiadau epilepsi (cy) épilepsie myoclonique (fr) صرع رمعي عضلي (ar)
skos:prefLabel	myoclonic epilepsy (en) Myoklonusepilepsia (fi) mioklonična epilepsija (sl) myoklon epilepsi (nn) ysgytiadau epilepsi (cy) épilepsie myoclonique (fr) صرع رمعي عضلي (ar)
name	myoclonic epilepsy (en) Myoklonusepilepsia (fi) mioklonična epilepsija (sl) myoklon epilepsi (nn) ysgytiadau epilepsi (cy) épilepsie myoclonique (fr) صرع رمعي عضلي (ar)
instance of	wds:Q11883686-D6273907-0A53-4E0C-985D-296814962FE5
instance of	disease
subclass of	wds:Q11883686-940C1F38-98DC-4B27-B0D7-A8E83292986A
subclass of	epilepsy
KEGG ID	wds:Q11883686-F73E551E-3868-4732-A502-139A8D36269A
KEGG ID	http://www.kegg.jp/entry/H01822
KEGG ID	H01822
GARD rare disease ID	wds:Q11883686-3AAD954A-B8FC-4C79-A994-CECDA1B191C0
GARD rare disease ID	7142
skos:altLabel	Epilepsies, Myoclonic (en) Ramsay-Huntin oireyhtymä (fi) Ramsay-Huntin syndrooma (fi) myoklonisk epilepsi (nn) myoklonusepilepsi (nn)
OpenAlex ID	wds:Q11883686-405E2458-1814-42BB-BAEA-14758D3E5595
UMLS CUI	wds:Q11883686-B9A8D70E-C142-4383-847A-4F80853A2E1E
MeSH descriptor ID	wds:Q11883686-74EC53E4-32EE-4BEF-ACC5-AFA85EEC8A24
Microsoft Academic ID	wds:Q11883686-1AA07C27-FD7D-4709-89B3-EF444F1C6699 wds:Q11883686-CE9CCE89-2642-4FE1-A11A-E4CE54A96250
MeSH tree code	wds:Q11883686-5E015B83-A4BE-45A0-BA65-E11E0EA9E136 wds:Q11883686-D53E9D79-C20A-45F7-8546-EA98E8DF7F8E
MeSH descriptor ID	http://id.nlm.nih.gov/mesh/D004831
Microsoft Academic ID	https://makg.org/entity/2775859823 https://makg.org/entity/2909642412
MeSH tree code	http://id.nlm.nih.gov/mesh/C10.228.140.490.375.130 http://id.nlm.nih.gov/mesh/C10.228.140.490.493.063
OpenAlex ID	C2775859823
UMLS CUI	C0014550
MeSH descriptor ID	D004831
Microsoft Academic ID	2775859823 2909642412
MeSH tree code	C10.228.140.490.375.130 C10.228.140.490.493.063
is owl:sameAs of	myoclonic epilepsy
is about of	myoclonic epilepsy https://www.wikidata.org/wiki/Special:EntityData/Q11883686 Myoclonic epilepsy https://ar.wikipedia.org/wiki/%D8%B5%D8%B1%D8%B9_%D8%B1%D9%85%D8%B9%D9%8A_%D8%B9%D8%B6%D9%84%D9%8A https://fi.wikipedia.org/wiki/Myoklonusepilepsia
is subclass of of	spinal muscular atrophy with progressive myoclonic epilepsy progressive myoclonus epilepsy early myoclonic encephalopathy juvenile myoclonic epilepsy benign adult familial myoclonic epilepsy epilepsy with myoclonic absences myoclonic epilepsy of infancy familial adult myoclonic epilepsy 4
is subclass of of	wds:Q55788679-4264796B-D46A-4B64-A4F8-AF04F0AF62C0 wds:Q56014312-05bce4e0-49d6-8340-74c5-49c6a6f1959d wds:Q56003194-b202860d-4ffe-bd53-dbe1-136cb6751c47 wds:Q7577468-875af3ab-44d1-c569-671f-a8b0c2c87e30 wds:Q543517-91b1b4dc-4182-3372-2243-08ef1a304cab wds:Q5326887-7b0811b6-43fa-4298-25fe-0e08cf46159d wds:Q7248853-d8e58510-4c85-eee8-ebe5-5fad35f696f9 wds:Q56014305-bd0f62ce-4e27-df18-4ceb-fc1859837559
is main subject of	De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF) Utility of high doses of melatonin as adjunctive anticonvulsant therapy in a child with severe myoclonic epilepsy: two years' experience. Delayed diagnosis of juvenile myoclonic epilepsy Focal structural changes and cognitive dysfunction in juvenile myoclonic epilepsy Thalamofrontal circuitry and executive dysfunction in recent-onset juvenile myoclonic epilepsy Risk-taking behavior in juvenile myoclonic epilepsy Motor system hyperconnectivity in juvenile myoclonic epilepsy: a cognitive functional magnetic resonance imaging study Pathogenic mechanism of a human mitochondrial tRNAPhe mutation associated with myoclonic epilepsy with ragged red fibers syndrome. Structural brain abnormalities in juvenile myoclonic epilepsy patients: volumetry and voxel-based morphometry Neuropsychological profiles of patients with juvenile myoclonic epilepsy and their siblings: a preliminary controlled experimental video-EEG case series Juvenile myoclonic epilepsy and idiopathic photosensitive occipital lobe epilepsy: is there overlap?

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