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Translation of "group small " (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
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
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
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
Definition: Disorder involving persistent dissocial or aggressive behaviour (meeting the overall criteria for F91.- and not merely comprising oppositional, defiant, disruptive behaviour) occurring in individuals who are generally well integrated into their peer group. | Conduct disorder, group type Group delinquency Offences in the context of gang membership Stealing in company with others Truancy from school
Définition: Trouble caractérisé par la présence d'un comportement dyssocial ou agressif (répondant aux critères généraux cités en F91.- et non limité à un comportement oppositionnel, provocateur ou perturbateur), se manifestant chez des enfants habituellement bien intégrés dans leur groupe d'âge. | Délinquance de groupe Délits commis en bande Ecole buissonnière Troubles des conduites, type en groupe Vols en groupe
WORLD HEALTH ORGANIZATION ICD-10: F91.2
WORLD HEALTH ORGANIZATION ICD-10: F91.2
A rare genetic axonal peripheral sensorimotor neuropathy with an X-linked recessive inheritance pattern and the neonatal to early childhood-onset of severe, slowly progressive, distal muscle weakness and atrophy (in particular of the peroneal group)
maladie de Charcot-Marie-Tooth liée à l'X type 4
SNOMEDCT-BE (in particular of the peroneal group) / 763400005
SNOMEDCT-BE (disorder) / 763400005
Shigella boydii (group C)
Shigella boydii (groupe C)
SNOMEDCT-CA (group C) / 186105003
SNOMEDCT-CA (groupe C) / 186105003
Charcot-Marie-Tooth disease, type 4F (CMT4F) is a demyelinating CMT peripheral sensorimotor polyneuropathy. It is a rare form of CMT4 but the few reported families are from diverse ethnic groups: Lebanese Shiite Muslims, Hispanic North Americans, Nor
maladie de Charcot-Marie-Tooth type 4F
SNOMEDCT-BE (CMT4F) is a demyelinating CMT peripheral sensorimotor polyneuropathy. It is a rare form of CMT4 but the few reported families are from diverse ethnic groups: Lebanese Shiite Muslims, Hispanic North Americans, Nor / 715801001
SNOMEDCT-BE (disorder) / 715801001
Mixed ethnic census group
groupe ethnique mixte selon le recensement
SNOMEDCT-CA (groupe ethnique) / 315239007
SNOMEDCT-CA (groupe ethnique) / 315239007
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'group small'
Date index:2022-03-03 -
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