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DAF syndrome
Histiocytosis X
Histiocytosis X syndrome
LCH
Langerhans cell histiocytosis
Langerhans' cell granulomatosis
Lipid histiocytosis
Lipoid histiocytosis
Lipoid histiocytosis
Niemann-Pick disease
Non-lipoid histiocytosis
Pulmonary LCH
Pulmonary Langerhans cell histiocytosis
Pulmonary eosinophilic granuloma
Pulmonary histiocytosis X
Sphingomyelin lipidosis
Sphingomyelinase deficiency
Unifocal Langerhans cell histiocytosis

Traduction de «non-lipoid histiocytosis » (Anglais → Néerlandais) :



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

ziekte van Niemann-Pick




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.]


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




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'non-lipoid histiocytosis' ->

Date index: 2021-11-05
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