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Translation of "disease sarcoidosis " (English → French) :
TERMINOLOGY
see also In-Context Translations below Sarcoidosis of lung
sarcoïdose pulmonaire
SNOMEDCT-BE (disorder) / 24369008
SNOMEDCT-BE (disorder) / 24369008
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
A rare disorder characterized by the combination of autoimmune intestinal disease, epileptic seizures and cerebral calcifications. Celiac disease and epilepsy manifest at a variable age. Celiac disease can present in a typical form with onset in the
syndrome de maladie coeliaque-calcifications cérébrales-épilepsie
SNOMEDCT-BE (disorder) / 722386009
SNOMEDCT-BE (disorder) / 722386009
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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'disease sarcoidosis'
Date index:2021-02-17 -
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