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
44 clinical trials for this condition and its sub-types, 1 tagged with Non-Langerhans cell histiocytosis itself.
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Sub-types of Non-Langerhans cell histiocytosis
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Niemann-Pick disease 10 trials · 22 incl. sub-types
4 sub-types
- Niemann-Pick disease type C 12 trials · 13 incl. sub-types Sub-types →
- Acid sphingomyelinase deficiency 7 trials · 10 incl. sub-types Sub-types →
- Niemann-Pick disease type E 0 trials
- Chronic neurovisceral acid sphingomyelinase deficiency 0 trials
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Erdheim-Chester disease 14 trials
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1 sub-type
- H syndrome 0 trials
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Juvenile xanthogranuloma 4 trials
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Xanthogranuloma 1 trial
1 sub-type
- Adult xanthogranuloma 0 trials
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Benign cephalic histiocytosis 0 trials
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Generalized eruptive histiocytosis 0 trials
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Multicentric reticulohistiocytosis 0 trials
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Necrobiotic xanthogranuloma 0 trials
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Papular xanthoma 0 trials
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Progressive nodular histiocytosis 0 trials
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Sea-blue histiocyte syndrome 0 trials
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Xanthoma disseminatum 0 trials