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Churg-Strauss
Lung involvement
Lung involvement+
Myopathy+
Polyarteritis with lung involvement
Renal tubulo-interstitial disorders+
Sjögren's syndrome with keratoconjunctivitis+
Systemic sclerosis with lung involvement+

Translation of "Lung involvement " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Libman-Sacks disease (I39.-*) Lupus pericarditis (I32.8*) Systemic lupus erythematosus with:kidney involvement (N08.5*, N16.4*) | lung involvement (J99.1*)

Lupus érythémateux disséminé avec atteinte des:poumons (J99.1*) | reins (N08.5*, N16.4*) | Maladie de Libman-Sacks (I39.-*) Péricardite lupique (I32.8*)
WORLD HEALTH ORGANIZATION ICD-10: M32.1+
WORLD HEALTH ORGANIZATION ICD-10: M32.1+


Sjögren's syndrome with:keratoconjunctivitis+ (H19.3*) | lung involvement+ (J99.1*) | myopathy+ (G73.7*) | renal tubulo-interstitial disorders+ (N16.4*)

Syndrome de Gougerot-Sjögren avec:atteinte pulmonaire+ (J99.1*) | kératoconjonctivite+ (H19.3*) | maladie rénale tubulo-interstitielle+ (N16.4*) | myopathie+ (G73.7*)
WORLD HEALTH ORGANIZATION ICD-10: M35.0
WORLD HEALTH ORGANIZATION ICD-10: M35.0


Systemic sclerosis with:lung involvement+ (J99.1*) | myopathy+ (G73.7*)

Sclérose systémique avec:atteinte pulmonaire+ (J99.1*) | myopathie+ (G73.7*)
WORLD HEALTH ORGANIZATION ICD-10: M34.8
WORLD HEALTH ORGANIZATION ICD-10: M34.8


Polyarteritis with lung involvement [Churg-Strauss]

Périartérite avec atteinte pulmonaire [Churg-Strauss]
WORLD HEALTH ORGANIZATION ICD-10: M30.1
WORLD HEALTH ORGANIZATION ICD-10: M30.1


A rare aggressive subtype of invasive breast carcinoma characterized by rapid growth, relatively large tumor size and a tendency to metastasize to distant organs, particularly the lungs, with relatively less frequent involvement of the axillary lymph

carcinome métaplasique du sein
SNOMEDCT-BE (disorder) / 763479005
SNOMEDCT-BE (disorder) / 763479005


A rare and isolated orofacial defect with manifestation of incomplete median clefts of both the lower lip (limited to the vermilion, with no muscle involvement) and upper lip (with muscle involvement), double labial frenulum and fusion of the upper g

fente labiale médiane supérieure et inférieure, forme familiale
SNOMEDCT-BE (limited to the vermilion, with no muscle involvement) and upper lip (with muscle involvement), double labial frenulum and fusion of the upper g / 718552009
SNOMEDCT-BE (disorder) / 718552009


Cheese-washer's lung Coffee-worker's lung Fishmeal-worker's lung Furrier's lung Sequoiosis

Maladie due au séquoïa Poumon des:fourreurs | laveurs de fromage | torréfacteurs de café | travailleurs de préparations alimentaires à base de poissons
WORLD HEALTH ORGANIZATION ICD-10: J67.8
WORLD HEALTH ORGANIZATION ICD-10: J67.8


A rare idiopathic skin disease with characteristics of widespread, congenital, superficial erosions and vesicles (often involving more than 75% of the body) which heal leaving scars with a supple, symmetrical, reticulated pattern, frequently resultin

dermatose érosive et vésiculaire congénitale
SNOMEDCT-BE (often involving more than 75% of the body) which heal leaving scars with a supple, symmetrical, reticulated pattern, frequently resultin / 773691007
SNOMEDCT-BE (disorder) / 773691007


A rare syndromic microphthalmia disorder with characteristics of microphthalmia with coloboma (which may involve the iris, ciliary body, choroid, retina and/or optic nerve), microcephaly, short stature and intellectual disability. Other eye abnormali

syndrome de micropthalmie colobomateuse-microcéphalie-déficience intellectuelle-petite taille liée à l'X
SNOMEDCT-BE (which may involve the iris, ciliary body, choroid, retina and/or optic nerve), microcephaly, short stature and intellectual disability. Other eye abnormali / 771148008
SNOMEDCT-BE (disorder) / 771148008


A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandib

syndrome de Mœbius
SNOMEDCT-BE (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandib / 89444000
SNOMEDCT-BE (disorder) / 89444000
IN-CONTEXT TRANSLATIONS


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'Lung involvement '

Date index:2024-04-21 -

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