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Erdheim-Chester Disease
Hierarchy: | ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Erdheim-Chester Disease 5 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Erdheim-Chester Disease 5 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Erdheim-Chester Disease 5 coordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Erdheim-Chester Disease 5 coordinate concepts∟ ∟ ∟ ∟ ∟ |
Broader terms: | |
History note: | Histiocytosis (1989-2002) | Histiocytosis, Langerhans-Cell (1988-2002) | Histiocytosis, Non-Langerhans-Cell (1991-2002) | Lipidosis (1979-2002) | Xanthomatosis (1979-2002)X |
historyNote*: | 2003
X |
publicMeSHNote*: | 2003
X |
Scope note: | A rare form of non-Langerhans-cell histiocytosis (HISTIOCYTOSIS, NON-LANGERHANS-CELL) with onset in middle age. The systemic disease is characterized by infiltration of lipid-laden macrophages, multinucleated giant cells, an inflammatory infiltrate of lymphocytes and histiocytes in the bone marrow, and a generalized sclerosis of the long bones.
X |
activeMeSHYear*: | |
dateCreated*: | 2002-07-03X |
dateEstablished*: | 2003-01-01X |
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Labels and equivalent concepts: | Erdheim-Chesterin tauti (fi) XErdheim-Chesterin sairaus (fi, replaced) Erdheim-Chesters sjukdom (sv) Granulomatosis, Lipid (en, replaced) Morbus Erdheim-Chester (la-FI, replaced) |
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