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Dermatomyosite
Dermatomyosite associée à une affection maligne
Dermatomyosite néonatale
Granulomatose de Wegener
Lupus erythémateux disséminé
Polymyosite
Polymyosite aiguë progressive
Polymyosite oedémateuse de Wagner-Unverricht
Sclérodermie
Syndrome de Gougerot-Sjögren
érythroedème myasthénique de Milian

Translation of "dermatomyosite " (French → English) :

dermatomyosite | érythroedème myasthénique de Milian | polymyosite aiguë progressive | polymyosite oedémateuse de Wagner-Unverricht

dermatomyositis
IATE - Health
IATE - Health


dermatomyosite | érythroedème myasthénique de Milian | polymyosite aiguë progressive

dermatomyositis
IATE - Health
IATE - Health


dermatomyosite

dermatomyositis
Épiderme et derme
Epidermis and Dermis


dermatomyosite/polymyosite

dermato/polymyositis
Épiderme et derme
Epidermis and Dermis






dermatomyosite associée à une affection maligne

Dermatomyositis with malignant disease
SNOMEDCT-CA (trouble) / 239901009
SNOMEDCT-CA (trouble) / 239901009


dermatomyosite néonatale

A very rare secondary neonatal autoimmune disease characterised by generalised weakness, severe hypotonia, absent or reduced deep tendon reflexes and highly elevated serum creatine kinase levels presenting in the neonatal period. Perifascicular atrop
SNOMEDCT-BE (disorder) / 774082004
SNOMEDCT-BE (disorder) / 774082004


dermatomyosite

Dermatomyositis
SNOMEDCT-BE (disorder) / 396230008
SNOMEDCT-BE (disorder) / 396230008


Troubles respiratoires au cours de:dermatomyosite (M33.0-M33.1+) | granulomatose de Wegener (M31.3+) | lupus erythémateux disséminé (M32.1+) | polymyosite (M33.2+) | sclérodermie (M34.8+) | syndrome de Gougerot-Sjögren (M35.0+)

Respiratory disorders in:dermatomyositis (M33.0-M33.1+) | polymyositis (M33.2+) | sicca syndrome [Sjögren] (M35.0+) | systemic:lupus erythematosus (M32.1+) | sclerosis (M34.8+) | Wegener's granulomatosis (M31.3+)
WORLD HEALTH ORGANIZATION ICD-10: J99.1*
WORLD HEALTH ORGANIZATION ICD-10: J99.1*




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dermatomyosite

Date index:2022-02-04 -

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