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Translation of "Myocloniques " (French → English) :
TERMINOLOGY
see also In-Context Translations below Convulsions néonatales bénignes (familiales) Crises non spécifiques:atoniques | cloniques | myocloniques | tonico-cloniques | toniques | Epilepsie (avec):absences de l'adolescence | absences de l'enfance [pyknolepsie] | crises [grand mal] au réveil | myoclonique bénigne de l'enfance | myoclonique [petit mal impulsif] juvénile
Benign:myoclonic epilepsy in infancy | neonatal convulsions (familial) | Childhood absence epilepsy [pyknolepsy] Epilepsy with grand mal seizures on awakening Juvenile:absence epilepsy | myoclonic epilepsy [impulsive petit mal] | Nonspecific epileptic seizures:atonic | clonic | myoclonic | tonic | tonic-clonic
WORLD HEALTH ORGANIZATION ICD-10: G40.3
WORLD HEALTH ORGANIZATION ICD-10: G40.3
Encéphalopathie myoclonique précoce symptomatique Epilepsie avec:absences myocloniques | crises astato-myocloniques | Spasmes infantiles Syndrome de:Lennox-Gastaut | West | Tic de Salaam
Epilepsy with:myoclonic absences | myoclonic-astatic seizures | Infantile spasms Lennox-Gastaut syndrome Salaam attacks Symptomatic early myoclonic encephalopathy West's syndrome
WORLD HEALTH ORGANIZATION ICD-10: G40.4
WORLD HEALTH ORGANIZATION ICD-10: G40.4
épilepsie myoclonique juvénile
Janz syndrome
SNOMEDCT-BE (disorder) / 6204001
SNOMEDCT-BE (disorder) / 6204001
épilepsie myoclonique progressive
Progressive myoclonic epilepsy
SNOMEDCT-BE (disorder) / 267581004
SNOMEDCT-BE (disorder) / 267581004
epilepsie myoclonique des encéphalopathies non-progressives
Myoclonic epilepsy in non-progressive encephalopathy
SNOMEDCT-BE (disorder) / 778047006
SNOMEDCT-BE (disorder) / 778047006
encéphalopathie myoclonique précoce
Early myoclonic encephalopathy
SNOMEDCT-BE (disorder) / 44423001
SNOMEDCT-BE (disorder) / 44423001
epilepsie myoclonique progressive avec dystonie
Progressive myoclonus epilepsy with dystonia
SNOMEDCT-BE (disorder) / 763349002
SNOMEDCT-BE (disorder) / 763349002
syndrome d'ataxie spastique-epilepsie myoclonique-neuropathie précoce
AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome
SNOMEDCT-BE (disorder) / 771469002
SNOMEDCT-BE (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome / 771469002
epilepsie myoclonique bénigne familiale de l'adulte
Autosomal dominant cortical myoclonus and epilepsy
SNOMEDCT-BE (disorder) / 717225001
SNOMEDCT-BE (disorder) / 717225001
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Myocloniques
Date index:2021-10-19 -
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