Non-Langerhans cell histiocytosis
MONDO:0015531Group of disorders which feature accumulations of active HISTIOCYTES and LYMPHOCYTES, but where the histiocytes are not LANGERHANS CELLS. The group includes HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; SINUS HISTIOCYTOSIS; xanthogranuloma; reticulohistiocytoma; juvenile XANTHOGRANULOMA; xanthoma disseminatum; as well as the lipid storage diseases (SEA-BLUE HISTIOCYTE SYNDROME; and NIEMANN-PICK DISEASES).
Also known as: non-Langerhans-cell histiocytosis, histiocytosis, non-Langerhans-cell
51 clinical trials for this condition and its sub-types.
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Erdheim-Chester disease
(14)
Niemann-Pick disease type C
(12)
Sinus histiocytosis with massive lymphadenopathy
(11)
Niemann-Pick disease
(10)
Acid sphingomyelinase deficiency
(7)
Juvenile xanthogranuloma
(4)
Niemann-Pick disease type A
(4)
Niemann-Pick disease, type C1
(2)
Indeterminate dendritic cell tumor
(1)
Niemann-Pick disease type B
(1)
Niemann-Pick disease, type C2
(1)
Xanthogranuloma
(1)
Adult xanthogranuloma
(0)
Benign cephalic histiocytosis
(0)
Chronic neurovisceral acid sphingomyelinase deficiency
(0)
Generalized eruptive histiocytosis
(0)
Hereditary progressive mucinous histiocytosis
(0)
H syndrome
(0)
Multicentric reticulohistiocytosis
(0)
Necrobiotic xanthogranuloma
(0)