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Aberrant pulmonary artery Agenesis
Anomaly
Benign cephalic histiocytosis
DAF syndrome
Histiocytosis X
Histiocytosis X syndrome
Hypoplasia
LCH
Langerhans cell histiocytosis
Langerhans' cell granulomatosis
Lipid histiocytosis
Lipoid histiocytosis
Malignant histiocytosis
Niemann-Pick disease
Of pulmonary artery
Pulmonary LCH
Pulmonary Langerhans cell histiocytosis
Pulmonary arteriovenous aneurysm
Pulmonary eosinophilic granuloma
Pulmonary histiocytosis X
Sphingomyelin lipidosis
Sphingomyelinase deficiency
Unifocal Langerhans cell histiocytosis

Translation of "Pulmonary histiocytosis X " (English → French) :

pulmonary eosinophilic granuloma | pulmonary histiocytosis X | pulmonary Langerhans cell histiocytosis | unifocal Langerhans cell histiocytosis | pulmonary LCH [Abbr.]

histiocytose langerhansienne pulmonaire | histiocytose langerhansienne pulmonaire de l'adulte | histiocytose pulmonaire | HL pulmonaire [Abbr.]
IATE - Health
IATE - Health


histiocytosis X | histiocytosis X syndrome | Langerhans' cell granulomatosis | Langerhans cell histiocytosis | LCH [Abbr.]

histiocytose à cellules de Langerhans | histiocytose X
IATE - Health
IATE - Health


DAF syndrome | lipid histiocytosis | lipoid histiocytosis (classical phosphatide) | Niemann-Pick disease | sphingomyelin lipidosis | sphingomyelinase deficiency

histiocytose lipoïdique essentielle | maladie de Niemann-Pick | sphingomyélinose
IATE - Health
IATE - Health


A rare congenital heart malformation with characteristics of tetralogy of Fallot (pulmonary stenosis, overriding aorta, ventricular septal defect and right ventricular hypertrophy), complete absence or rudimentary pulmonary valve that is both stenoti

syndrome d'agénésie de la valve pulmonaire-tétralogie de Fallot-absence du canal artériel
SNOMEDCT-BE (pulmonary stenosis, overriding aorta, ventricular septal defect and right ventricular hypertrophy), complete absence or rudimentary pulmonary valve that is both stenoti / 766976003
SNOMEDCT-BE (disorder) / 766976003


Aberrant pulmonary artery Agenesis | Aneurysm, congenital | Anomaly | Hypoplasia | of pulmonary artery | Pulmonary arteriovenous aneurysm

Agénésie | Anévrisme congénital | Anomalie | Hypoplasie | de l'artère pulmonaire | Anévrisme pulmonaire artério-veineux Artère pulmonaire aberrante
WORLD HEALTH ORGANIZATION ICD-10: Q25.7
WORLD HEALTH ORGANIZATION ICD-10: Q25.7


Benign cephalic histiocytosis

histiocytose céphalique bénigne
SNOMEDCT-BE (disorder) / 255192005
SNOMEDCT-BE (disorder) / 255192005


A rare benign non-Langerhans cell histiocytosis characterized by childhood or adolescence onset of multiple, small, asymptomatic, slowly progressing, skin-colored to red-brown papules with predilection for the face, dorsal hands, forearms and legs, w

histiocytose progressive mucineuse héréditaire
SNOMEDCT-BE (disorder) / 771300001
SNOMEDCT-BE (disorder) / 771300001


Eosinophilic granuloma Hand-Schüller-Christian disease Histiocytosis X (chronic)

Granulome éosinophile Histiocytose X (chronique) Maladie de Hand-Schüller-Christian
WORLD HEALTH ORGANIZATION ICD-10: D76.0
WORLD HEALTH ORGANIZATION ICD-10: D76.0


Malignant histiocytosis

Histiocytose maligne
WORLD HEALTH ORGANIZATION ICD-10: C96.1
WORLD HEALTH ORGANIZATION ICD-10: C96.1




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'Pulmonary histiocytosis X'

Date index:2021-11-26 -

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