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Cataracte
Congénital
Côlon
Genou varum congénital
Intestin
Présent à la naissance
Syndrome d'ataxie-myosis congénital
Syndrome du grêle court congénital

Translation of "Congénital " (French → English) :

TERMINOLOGY
see also In-Context Translations below
congénital | présent à la naissance

congenital | from birth
UGENT - Medical terms -
UGENT - Medical terms -


Absence congénitale de la rotule Genu valgum congénital Genu varum congénital Luxation congénitale de la rotule Rotule rudimentaire

Congenital:absence of patella | dislocation of patella | genu:valgum | varum | Rudimentary patella
WORLD HEALTH ORGANIZATION ICD-10: Q74.1
WORLD HEALTH ORGANIZATION ICD-10: Q74.1


cataracte | 1) opacité du cristallin (= congénital) - 2) opacification du cristallin (= sénile)

cataract
UGENT - Medical terms -
UGENT - Medical terms -


Dédoublement de l'estomac Déplacement congénital de l'estomac Diverticule congénital de l'estomac Estomac en sablier, congénital Mégalogastrie Microgastrie

Congenital:displacement of stomach | diverticulum of stomach | hourglass stomach | Duplication of stomach Megalogastria Microgastria
WORLD HEALTH ORGANIZATION ICD-10: Q40.2
WORLD HEALTH ORGANIZATION ICD-10: Q40.2


Diverticule congénital de l'intestin Diverticulite congénitale du côlon Dolichocôlon Méga-appendice Mégaduodénum Microcôlon Syndrome de l'anse borgne, congénital Transposition de:appendice | côlon | intestin

Congenital:blind loop syndrome | diverticulitis, colon | diverticulum, intestine | Dolichocolon Megaloappendix Megaloduodenum Microcolon Transposition of:appendix | colon | intestine
WORLD HEALTH ORGANIZATION ICD-10: Q43.8
WORLD HEALTH ORGANIZATION ICD-10: Q43.8


Buphtalmie Glaucome du nouveau-né Hydrophtalmie Kératoglobe congénital avec glaucome Macrocornée ou mégalocornée avec glaucome Macrophtalmie au cours d'un glaucome congénital

Buphthalmos Glaucoma of newborn Hydrophthalmos Keratoglobus, congenital, with glaucoma Macrocornea with glaucoma Macrophthalmos in congenital glaucoma Megalocornea with glaucoma
WORLD HEALTH ORGANIZATION ICD-10: Q15.0
WORLD HEALTH ORGANIZATION ICD-10: Q15.0


syndrome d'ataxie-myosis congénital

Autosomal dominant spastic ataxia type 7
SNOMEDCT-BE (disorder) / 763669001
SNOMEDCT-BE (disorder) / 763669001


syndrome d'absence de dermatoglyphes-miliaire congénital

Baird syndrome
SNOMEDCT-BE (disorder) / 719595002
SNOMEDCT-BE (disorder) / 719595002


syndrome du grêle court congénital

A rare intestinal disorder of neonates of unknown aetiology. Patients are born with a short small bowel (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhoea, vomiting and failure to thrive.
SNOMEDCT-BE (disorder) / 715201005
SNOMEDCT-BE (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhoea, vomiting and failure to thrive. / 715201005


genou varum congénital

Congenital bowleg
SNOMEDCT-BE (disorder) / 79168008
SNOMEDCT-BE (disorder) / 79168008
IN-CONTEXT TRANSLATIONS


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Congénital

Date index:2021-04-12 -

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