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Affection du cerveau
Encéphalopathie
Encéphalopathie anoxique
Encéphalopathie hépatique
Encéphalopathie myoclonique précoce
Encéphalopathie nécrosante aigüe familiale
Encéphalopathie par COVID-19
Encéphalopathie épileptique-dyskinétique infantile

Translation of "Encéphalopathie " (French → English) :

TERMINOLOGY
see also In-Context Translations below
encéphalopathie | affection du cerveau

encephalopathy | brain disease
UGENT - Medical terms -
UGENT - Medical terms -


encéphalopathie épileptique-dyskinétique infantile

Infantile epileptic dyskinetic encephalopathy
SNOMEDCT-BE (disorder) / 771223000
SNOMEDCT-BE (disorder) / 771223000


encéphalopathie myoclonique précoce

Early myoclonic encephalopathy
SNOMEDCT-BE (disorder) / 44423001
SNOMEDCT-BE (disorder) / 44423001


encéphalopathie par COVID-19

Encephalopathy due to COVID-19
SNOMEDCT-BE (disorder) / 1240561000000108
SNOMEDCT-BE (disorder) / 1240561000000108


encéphalopathie auto-immune avec parasomnie et apnée obstructive du sommeil

Anti-IgLON5 disease
SNOMEDCT-BE (disorder) / 765751002
SNOMEDCT-BE (disorder) / 765751002


encéphalopathie associée à une hyperméthioninémie par déficit en adénosine kinase

A rare inborn error of metabolism characterized by persistent hypermethioninemia with increased levels of S-adenosylmethionine and S-adenosylhomocysteine which manifests with encephalopathy, severe global developmental delay, mild to severe liver dys
SNOMEDCT-BE (disorder) / 763721006
SNOMEDCT-BE (disorder) / 763721006


encéphalopathie nécrosante aigüe familiale

A potentially fatal neurological disease with characteristics of neuropathological lesions principally involving the brainstem, thalamus and putamen. It has been described in 11 members of one family. Onset occurs during early childhood, typically a
SNOMEDCT-BE (disorder) / 723359002
SNOMEDCT-BE (disorder) / 723359002


encéphalopathie anoxique

Anoxic brain damage
SNOMEDCT-BE (disorder) / 389098007
SNOMEDCT-BE (disorder) / 389098007


encéphalopathie hépatique

Gaustad's syndrome
SNOMEDCT-BE (disorder) / 13920009
SNOMEDCT-BE (disorder) / 13920009


syndrome d'encéphalopathie épileptique infantile précoce-cécité corticale-déficience intellectuelle-dysmorphie faciale

Epilepsy, cortical blindness, intellectual disability, facial dysmorphism syndrome
SNOMEDCT-BE (disorder) / 773548008
SNOMEDCT-BE (disorder) / 773548008
IN-CONTEXT TRANSLATIONS


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Encéphalopathie

Date index:2022-04-10 -

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