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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
Lung-relted
Niemann-Pick disease
Of pulmonary artery
Other histiocytosis syndromes
Pulmonary
Pulmonary LCH
Pulmonary Langerhans cell histiocytosis
Pulmonary arteriovenous aneurysm
Pulmonary eosinophilic granuloma
Pulmonary histiocytosis X
Sphingomyelin lipidosis
Sphingomyelinase deficiency
Unifocal Langerhans cell histiocytosis

Traduction de «pulmonary histiocytosis » (Anglais → Néerlandais) :

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

pulmonale Langerhanscel histiocytose | PLHC [Abbr.]


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

histiocytose-X | Langerhans Cel Histiocytose | LHC [Abbr.]


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

ziekte van Niemann-Pick


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

agenesie van pulmonalisklep, tetralogie van Fallot, afwezigheid van ductus arteriosus-syndroom


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

aberrante 'arteria pulmonalis' | agenesievan arteria pulmonalis | aneurysmavan arteria pulmonalis | anomalievan arteria pulmonalis | arterioveneus aneurysmavan arteria pulmonalis | hypoplasievan arteria pulmonalis


Benign cephalic histiocytosis

goedaardige cefalische histiocytose


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

erfelijke progressieve mucineuze histiocytose


Other histiocytosis syndromes

overige histiocytosesyndromen


Reticulohistiocytoma (giant-cell) Sinus histiocytosis with massive lymphadenopathy Xanthogranuloma

reticulohistiocytoom (reuscel) | sinushistiocytose met massale lymfadenopathie | xanthogranuloom


pulmonary | lung-relted

pulmonair | met betrekking tot de longen


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