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Translation of "vascular disease " (English → French) :
TERMINOLOGY
see also In-Context Translations below A very rare genetic vascular disease of autosomal recessive inheritance, described in less than 20 patients to date. The disease has manifestations of adult-onset (as early as the second decade of life) isolated calcification of the arteries of the l
syndrome héréditaire de calcification artérielle et articulaire
SNOMEDCT-BE (as early as the second decade of life) isolated calcification of the arteries of the l / 718602007
SNOMEDCT-BE (disorder) / 718602007
A rare benign retinal vascular disease characterised by solitary or multiple, unilateral or bilateral, intra-retinal tumour(s), usually located in the peripheral infero-temporal quadrant, and often associated with sub and intraretinal exudates, epire
masses télangiectasiques périphériques
SNOMEDCT-BE (s), usually located in the peripheral infero-temporal quadrant, and often associated with sub and intraretinal exudates, epire / 771235001
SNOMEDCT-BE (disorder) / 771235001
vascular | blood vessel-related
vasculaire | relatif aux vaisseaux sanguins
UGENT - Medical terms -
UGENT - Medical terms -
Care given to improve the quality of life of patients who have a serious or life-threatening disease. The goal of symptom management is to prevent or treat as early as possible the symptoms of a disease, side effects caused by treatment of a disease,
gestion des symptômes
SNOMEDCT-BE (procedure) / 713148004
SNOMEDCT-BE (procedure) / 713148004
Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo
ataxie spinocérébelleuse type 38
SNOMEDCT-BE (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo / 734021001
SNOMEDCT-BE (disorder) / 734021001
A rare non-hereditary condition characterised by gastrointestinal stromal tumours (GIST), pulmonary chondromas and extraadrenal paragangliomas. Less than 100 cases have been reported worldwide. The disease primarily affects young women (mean age of o
triade de Carney
SNOMEDCT-BE (GIST), pulmonary chondromas and extraadrenal paragangliomas. Less than 100 cases have been reported worldwide. The disease primarily affects young women (mean age of o / 733492003
SNOMEDCT-BE (disorder) / 733492003
A mitochondrial disease due to a defect in mitochondrial protein synthesis resulting in deficiency of respiratory chain complexes I, III and IV in the cardiac and skeletal muscle and brain. The disease has characteristics of severe hypertrophic cardi
déficit combiné de la phosphorylation oxydative type 8
SNOMEDCT-BE (disorder) / 733600007
SNOMEDCT-BE (disorder) / 733600007
A variant of lichen planopilaris characterised by the clinical triad of progressive cicatricial (scarring) alopecia of the scalp, follicular keratotic papules on glabrous skin, and variable alopecia of the axillae and groin. It is a very rare disease
syndrome de Graham Little-Piccardi-Lassueur
SNOMEDCT-BE (scarring) alopecia of the scalp, follicular keratotic papules on glabrous skin, and variable alopecia of the axillae and groin. It is a very rare disease / 718215008
SNOMEDCT-BE (disorder) / 718215008
A form of Parkinson disease with age of onset between 21 and 45 years, rigidity, painful cramps followed by tremor, bradykinesia, dystonia, gait complaints, falls and other non-motor symptoms. A slow disease progression and a more pronounced response
maladie de Parkinson à début précoce
SNOMEDCT-BE (disorder) / 715345007
SNOMEDCT-BE (disorder) / 715345007
A rare severe and life-threatening genetic disease occurring during the neonatal period. The disease has characteristics of classical Marfan syndrome manifestations in addition to facial dysmorphism (megalocornea, iridodonesis, ectopia lentis, crumpl
syndrome de Marfan néonatal
SNOMEDCT-BE (megalocornea, iridodonesis, ectopia lentis, crumpl / 763839005
SNOMEDCT-BE (disorder) / 763839005
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'vascular disease'
Date index:2021-01-24 -
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