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Translation of "Terminal " (English → French) :
TERMINOLOGY
see also In-Context Translations below Terminal apnea
apnée terminale
SNOMEDCT-BE (finding) / 50636009
SNOMEDCT-BE (finding) / 50636009
Terminal osseous dysplasia and pigmentary defect syndrome
syndrome de dysplasie osseuse terminale-défauts de pigmentation
SNOMEDCT-BE (disorder) / 723578001
SNOMEDCT-BE (disorder) / 723578001
Terminal colostomy
colostomie terminale
SNOMEDCT-BE (morphologic abnormality) / 261030007
SNOMEDCT-BE (morphologic abnormality) / 261030007
Computer terminal
terminal informatique
SNOMEDCT-BE (physical object) / 467836009
SNOMEDCT-BE (physical object) / 467836009
Terminal bronchiole
entière bronchiole terminale
SNOMEDCT-BE (body structure) / 278981008
SNOMEDCT-BE (body structure) / 278981008
A very rare congenital malformation of the digits with the absence of the middle phalanges (usually of digits two to five), nail dysplasia and duplicated terminal phalanx of the thumb. Has been described in patients from two unrelated families.
brachydactylie type A5
SNOMEDCT-BE (usually of digits two to five), nail dysplasia and duplicated terminal phalanx of the thumb. Has been described in patients from two unrelated families. / 720570007
SNOMEDCT-BE (disorder) / 720570007
A malformation syndrome with the combination of bilateral coloboma of macula, horizontal pendular nystagmus, severe visual loss and brachydactyly type B. The hand and feet defects comprise shortening of the middle and terminal phalanges of the second
syndrome de colobome maculaire-brachydactylie type B
SNOMEDCT-BE (disorder) / 717785002
SNOMEDCT-BE (disorder) / 717785002
An extremely rare genetic endocrine disease with characteristics of primary adrenal insufficiency, dystrophic myopathy, hepatic steatosis, severe psychomotor delay, megalocornea, failure to thrive, chronic constipation, and terminal bladder ectasia w
adrénomyodystrophie
SNOMEDCT-BE (disorder) / 763311001
SNOMEDCT-BE (disorder) / 763311001
Syndrome with characteristics of caudal appendage, short terminal phalanges, deafness, cryptorchidism, intellectual deficit, short stature and dysmorphism. It has been described in monozygotic twin boys.
syndrome d'appendice caudal-surdité
SNOMEDCT-BE (disorder) / 726621009
SNOMEDCT-BE (disorder) / 726621009
The association of X-linked Alport syndrome with leiomyomatosis of the oesophagus, tracheobronchial tree or female genitals has been reported in more than 30 families. The disease is due to a deletion involving the 5' terminal region of both COL4A5 a
syndrome d'Alport lié à l'X-léiomyomatose diffuse
SNOMEDCT-BE (disorder) / 726106004
SNOMEDCT-BE (disorder) / 726106004
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'Terminal'
Date index:2023-06-26 -
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