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Ablepharon Absence or agenesis of cilia
Accessory eye muscle
Congenital fistula of lip
Congenital malformations of lips
Downstream lip of hood
Entrance lip of hood
Exit lip of hood
Eyelid
Interpreting lip movement
Interpreting lip movements
Lip reading
Lip sync
Lip synchronisation
Lip synchronization
Lip-reading
Lower lip of hood
Malformation of lip NOS
Upper lip of hood
Upstream lip of hood
Van der Woude's syndrome

Translation of "Malformation lip NOS " (English → French) :

interpreting lip movement | lip-reading | interpreting lip movements | lip reading

lecture labiale | lecture sur les lèvres
knowledge
Savoir


lip sync | lip synchronisation | lip synchronization

doublage | postsynchronisation | synchronisation labiale
IATE - Culture and religion | Electronics and electrical engineering
IATE - Culture and religion | Electronics and electrical engineering


downstream lip of hood | exit lip of hood | lower lip of hood

lèvre inférieure de la hotte
IATE - Natural and applied sciences
IATE - Natural and applied sciences


entrance lip of hood | upper lip of hood | upstream lip of hood

lèvre supérieure de la hotte
IATE - Natural and applied sciences
IATE - Natural and applied sciences


Congenital:fistula of lip | malformation of lip NOS | Van der Woude's syndrome

Fistule congénitale de la lèvre Malformation congénitale de la lèvre SAI Syndrome de Van der Woude
WORLD HEALTH ORGANIZATION ICD-10: Q38.0
WORLD HEALTH ORGANIZATION ICD-10: Q38.0


A rare and isolated orofacial defect with manifestation of incomplete median clefts of both the lower lip (limited to the vermilion, with no muscle involvement) and upper lip (with muscle involvement), double labial frenulum and fusion of the upper g

fente labiale médiane supérieure et inférieure, forme familiale
SNOMEDCT-BE (limited to the vermilion, with no muscle involvement) and upper lip (with muscle involvement), double labial frenulum and fusion of the upper g / 718552009
SNOMEDCT-BE (disorder) / 718552009


Congenital malformations of lips

Malformations congénitales des lèvres
WORLD HEALTH ORGANIZATION ICD-10: Q38.0
WORLD HEALTH ORGANIZATION ICD-10: Q38.0


A rare non-syndromic cerebellar malformation with characteristics of loss of volume in the right or left cerebellar hemisphere, with intact vermis and no other neurological anomalies (normal cerebral hemispheres, fourth ventricle, pons, medulla and m

hypoplasie isolée unilatérale des hémisphères cérébelleux
SNOMEDCT-CA (normal cerebral hemispheres, fourth ventricle, pons, medulla and m / 766934006
SNOMEDCT-CA (trouble) / 766934006


Syndrome with characteristics of infantile symmetrical distal muscle weakness and atrophy of the lower limbs, bilateral anterior polar cataracts and Dandy-Walker malformation. It has been described in two brothers. No sensorineural or cognitive defic

syndrome d'amyotrophie spinale-malformation de Dandy-Walker-cataracte
SNOMEDCT-BE (disorder) / 723612001
SNOMEDCT-BE (disorder) / 723612001


Ablepharon Absence or agenesis of:cilia | eyelid | Accessory:eye muscle | Blepharophimosis, congenital Coloboma of eyelid Congenital malformation of eyelid NOS

Ablépharie Absence ou agénésie de:cils | paupière | Blépharophimosis congénital Colobome de la paupière Malformation congénitale de la paupière SAI Muscle oculaire surnuméraire Paupière surnuméraire
WORLD HEALTH ORGANIZATION ICD-10: Q10.3
WORLD HEALTH ORGANIZATION ICD-10: Q10.3




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'Malformation lip NOS'

Date index:2021-06-02 -

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