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Paresis
Partial paralysis

Translation of "Partial " (English → French) :

TERMINOLOGY
see also In-Context Translations below
46,XY partial gonadal dysgenesis

dysgénésie gonadique partielle 46,XY
SNOMEDCT-BE (disorder) / 725045004
SNOMEDCT-BE (disorder) / 725045004


A partial autosomal monosomy with characteristics of a variable combination of developmental delay, intellectual disability, ectodermal, genitourinary and minor cardiac anomalies and specific dysmorphic features (prominent forehead and low-set ears).

monosomie non distale 12q
SNOMEDCT-BE (prominent forehead and low-set ears). / 782694003
SNOMEDCT-BE (disorder) / 782694003


A dysostosis with predominant vertebral and costal involvement and characteristics of oropharyngeal atresia, mild mandibulofacial dysostosis, auricular malformations, and costovertebral anomalies (hemivertebrae, block vertebra, partial fusion of the

syndrome d'imperforation de l'oropharynx-anomalies costovertébrales
SNOMEDCT-BE (hemivertebrae, block vertebra, partial fusion of the / 771185000
SNOMEDCT-BE (disorder) / 771185000


Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures

Epilepsie et syndromes épileptiques symptomatiques définis par leur localisation (focale, partielle) avec des crises partielles complexes
WORLD HEALTH ORGANIZATION ICD-10: G40.2
WORLD HEALTH ORGANIZATION ICD-10: G40.2


Localization-related (focal)(partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures

Epilepsie et syndromes épileptiques symptomatiques définis par leur localisation (focale, partielle) avec crises partielles simples
WORLD HEALTH ORGANIZATION ICD-10: G40.1
WORLD HEALTH ORGANIZATION ICD-10: G40.1


An extremely rare syndrome described in three members of a family (a mother and her two children) with the association of various ocular abnormalities (partial or complete aniridia, ptosis, pendular nystagmus, corneal pannus, persistent pupillary mem

syndrome d'aniridie-ptosis-déficience intellectuelle-obésité
SNOMEDCT-BE (a mother and her two children) with the association of various ocular abnormalities (partial or complete aniridia, ptosis, pendular nystagmus, corneal pannus, persistent pupillary mem / 720987001
SNOMEDCT-BE (disorder) / 720987001


A multiple congenital anomalies/dysmorphic syndrome with characteristics of multiple skeletal malformations (short femora and humeri, bilateral absence of metatarsal and metacarpal bone in hands and feet, bilateral partial syndactyly of fingers and t

syndrome de Verloove-Van Horick-Brubakk
SNOMEDCT-BE (short femora and humeri, bilateral absence of metatarsal and metacarpal bone in hands and feet, bilateral partial syndactyly of fingers and t / 764697003
SNOMEDCT-BE (disorder) / 764697003


paresis | partial paralysis

parésie | paralysie légère ou incomplète
UGENT - Medical terms -
UGENT - Medical terms -


A very rare form of familial partial lipodystrophy of unknown aetiology characterised by loss of adipose tissue that is confined to the limbs and a normal or increased fat distribution of the face, neck, and trunk. Arterial hypertension and diabetes

lipodystrophie partielle familiale type Köbberling
SNOMEDCT-BE (disorder) / 725035001
SNOMEDCT-BE (disorder) / 725035001


A rare chromosomal anomaly syndrome resulting from partial trisomy of the long arm of chromosome 20 with high phenotypic variability. The disease has characteristics of neurodevelopmental delay, cardiac malformations (ventricular septal defect, coarc

trisomie distale 20q
SNOMEDCT-BE (ventricular septal defect, coarc / 764500002
SNOMEDCT-BE (disorder) / 764500002
IN-CONTEXT TRANSLATIONS


Others have searched : xy partial gonadal dysgenesis    paresis    partial paralysis    Partial    


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'Partial'

Date index:2023-11-25 -

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