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Arthropathy in leukaemia
Benign cephalic histiocytosis
DAF syndrome
Fat
Histiocytosis X
Histiocytosis X syndrome
LCH
Langerhans cell histiocytosis
Langerhans' cell granulomatosis
Lipid
Lipid histiocytosis
Lipoid histiocytosis
Malignant histiocytosis
Multiple myeloma
Niemann-Pick disease
Other histiocytosis syndromes
Pulmonary LCH
Pulmonary Langerhans cell histiocytosis
Pulmonary eosinophilic granuloma
Pulmonary histiocytosis X
Sphingomyelin lipidosis
Sphingomyelinase deficiency
Unifocal Langerhans cell histiocytosis

Vertaling van "lipid histiocytosis " (Engels → Nederlands) :

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

ziekte van Niemann-Pick


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

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


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

pulmonale Langerhanscel histiocytose | PLHC [Abbr.]


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


A form of non-Langerhans cell histiocytosis with characteristics of cutaneous presentation of solitary or disseminated yellow to orange-brown papular or papulonodular, noncoalescent, asymptomatic skin lesions located predominantly on the head, neck,

papulair xanthoom


Arthropathy in:leukaemia (C91-C95+) | malignant histiocytosis (C96.1+) | multiple myeloma (C90.0+)

artropathie bij | leukemie (C91-C95) | artropathie bij | maligne histiocytose (C96.8) | artropathie bij | multipel myeloom (C90.0)


Other histiocytosis syndromes

overige histiocytosesyndromen


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

reticulohistiocytoom (reuscel) | sinushistiocytose met massale lymfadenopathie | xanthogranuloom




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