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Translation of "small vessel " (English → French) :
TERMINOLOGY
see also In-Context Translations below An inherited group of small vessel diseases comprised of cerebroretinal vasculopathy (CRV), hereditary vascular retinopathy (HRV) and hereditary endotheliopathy with retinopathy, nephropathy and stroke all exhibiting progressive visual impairment as
vasculopathie rétinienne avec leucoencéphalopathie cérébrale et manifestations systémiques
SNOMEDCT-CA (CRV), hereditary vascular retinopathy (HRV) and hereditary endotheliopathy with retinopathy, nephropathy and stroke all exhibiting progressive visual impairment as / 783787000
SNOMEDCT-CA (trouble) / 783787000
blood vessel bursa cartilage fascia fat ligament, except uterine lymphatic vessel muscle synovia tendon (sheath)
aponévrose bourse séreuse cartilage ligament, sauf de l'utérus muscle synoviale tendon (gaine) tissu adipeux vaisseau:lymphatique | sanguin |
WORLD HEALTH ORGANIZATION ICD-10: C49
WORLD HEALTH ORGANIZATION ICD-10: C49
Primary pigmented nodular adrenocortical disease (PPNAD) is a form of bilateral adrenocortical hyperplasia that is often associated with adrenocorticotrophin hormone independent Cushing syndrome. The disease has characteristics of small to normal siz
dysplasie micronodulaire pigmentée des surrénales
SNOMEDCT-BE (PPNAD) is a form of bilateral adrenocortical hyperplasia that is often associated with adrenocorticotrophin hormone independent Cushing syndrome. The disease has characteristics of small to normal siz / 719274008
SNOMEDCT-BE (disorder) / 719274008
Small-for-dates Small-and-light-for-dates
Petit et léger pour l'âge gestationnel Petit pour l'âge gestationnel
WORLD HEALTH ORGANIZATION ICD-10: P05.1
WORLD HEALTH ORGANIZATION ICD-10: P05.1
An extremely rare subtype of renal cell carcinoma most frequently characterized by a small, solitary, well-circumscribed, unencapsulated renal tumor composed of multiple small to medium-sized cysts with a white or gray, spongy (bubble wrap-like ) cut
carcinome rénal tubulokystique
SNOMEDCT-BE (bubble wrap-like") cut / 733603009
SNOMEDCT-BE (disorder) / 733603009
This syndrome has characteristics of X-linked intellectual deficit and mild variable manifestations, including short stature, small head circumference, sloping forehead, hearing loss, abnormally shaped ears, and small testes. It has been described in
déficience intellectuelle liée à l'X type Abidi
SNOMEDCT-BE (disorder) / 719018008
SNOMEDCT-BE (disorder) / 719018008
Small bowel
intestin grêle
SNOMEDCT-BE (body structure) / 30315005
SNOMEDCT-BE (body structure) / 30315005
A rare form of porokeratosis occurring mainly in adolescence and characterised by small pruritic or painful keratotic papules that first appear on the palms and soles, and may gradually become generalised. The prevalence is unknown but it is one of t
porokératose palmoplantaire et disséminée
SNOMEDCT-BE (disorder) / 718218005
SNOMEDCT-BE (disorder) / 718218005
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.
syndrome du grêle court congénital
SNOMEDCT-BE (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhoea, vomiting and failure to thrive. / 715201005
SNOMEDCT-BE (disorder) / 715201005
Small bowel obstruction
obstruction de l'intestin grêle
SNOMEDCT-BE (disorder) / 281255004
SNOMEDCT-BE (disorder) / 281255004
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'small vessel'
Date index:2023-12-18 -
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