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Lipodystrophie partielle acquise
Lipodystrophie partielle familiale type Köbberling
Monosomie partielle 5p
Trisomie partielle du chromosome 6
Trisomie partielle du chromosome 7
épilepsie partielle

Translation of "partiel " (French → English) :

TERMINOLOGY
see also In-Context Translations below
trisomie partielle du chromosome 6

Duplication of chromosome 6
SNOMEDCT-BE (disorder) / 726345000
SNOMEDCT-BE (disorder) / 726345000


trisomie partielle du chromosome 7

Duplication of chromosome 7
SNOMEDCT-BE (disorder) / 726346004
SNOMEDCT-BE (disorder) / 726346004


Epilepsie et syndromes épileptiques symptomatiques définis par leur localisation (focale, partielle) avec crises partielles simples

Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures
WORLD HEALTH ORGANIZATION ICD-10: G40.1
WORLD HEALTH ORGANIZATION ICD-10: G40.1


Epilepsie et syndromes épileptiques symptomatiques définis par leur localisation (focale, partielle) avec des crises partielles complexes

Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures
WORLD HEALTH ORGANIZATION ICD-10: G40.2
WORLD HEALTH ORGANIZATION ICD-10: G40.2


epilepsie bénigne partielle de l'enfant avec crises partielles complexes

A rare infantile epilepsy syndrome characterized by complex partial seizures presenting with motion arrest, decreased responsiveness, staring, automatisms and mild clonic movements, with or without apnea, normal interictal EEG and focal, mostly tempo
SNOMEDCT-BE (disorder) / 770624005
SNOMEDCT-BE (disorder) / 770624005


monosomie partielle 5p

Cri du chat syndrome
SNOMEDCT-BE (disorder) / 70173007
SNOMEDCT-BE (disorder) / 70173007


épilepsie partielle

Local convulsion
SNOMEDCT-BE (disorder) / 29753000
SNOMEDCT-BE (disorder) / 29753000


epilepsie partielle bénigne du nourrisson avec crises généralisées secondaires

A rare infantile epilepsy syndrome characterised by seizures presenting with motion arrest and staring. They are followed by generalised tonic-clonic convulsions with normal interictal EEG and focal paroxysmal discharges, followed by generalisation i
SNOMEDCT-BE (disorder) / 771141002
SNOMEDCT-BE (disorder) / 771141002


lipodystrophie partielle familiale type Köbberling

A very rare form of familial partial lipodystrophy of unknown aetiology characterised by loss of adipose tissue that is confined to the limbs and a normal or increased fat distribution of the face, neck, and trunk. Arterial hypertension and diabetes
SNOMEDCT-BE (disorder) / 725035001
SNOMEDCT-BE (disorder) / 725035001


lipodystrophie partielle acquise

Barraquer syndrome
SNOMEDCT-BE (disorder) / 75659004
SNOMEDCT-BE (disorder) / 75659004
IN-CONTEXT TRANSLATIONS


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partiel

Date index:2024-02-15 -

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