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Mixed Connective Tissue Disease
Hierarchy: | |
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Annotation: | disease entity: read definition & do not confuse with CONNECTIVE TISSUE DISEASES; DF: MCTD
X |
History note: | Collagen Diseases (1972-1978) | Lupus Erythematosus, Systemic (1972-1978) | Scleroderma, Systemic (1972-1978)X |
historyNote*: | 79
X |
publicMeSHNote*: | 79
X |
Scope note: | A syndrome with overlapping clinical features of systemic lupus erythematosus, scleroderma, polymyositis, and Raynaud's phenomenon. The disease is differentially characterized by high serum titers of antibodies to ribonuclease-sensitive extractable (saline soluble) nuclear antigen and a "speckled" epidermal nuclear staining pattern on direct immunofluorescence.
X |
activeMeSHYear*: | 1993 | 1994 | 1995 | 1996 | 1997 | 1998 | 1999 | 2000 | 2001 | 2002 | 2003 | 2004 | 2005 | 2006 | 2007X |
dateCreated*: | 1978-05-15X |
dateEstablished*: | 1979-01-01X |
dateRevised*: | 1992-05-22X |
recordAuthorizer*: | PLSX |
recordMaintainer*: | PLSX |
recordOriginator*: | AEPX |
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Labels and equivalent concepts: | Sekamuotoinen sidekudossairaus (fi) XSekamuotoinen sidekudostauti (fi, replaced) Systeeminen sidekudostauti (fi, replaced) MCTD-syndrooma (fi, replaced) MCTD-oireyhtymä (fi, replaced) MCTD (fi, replaced) Blandad bindvävssjukdom (sv) Bindvävssjukdom, blandad (sv, replaced) MCTD (sv, replaced) MCTD (en, replaced) Sharp Syndrome (en, replaced) Connective Tissue Disease, Mixed (en, replaced) Mixed connective tissue disease (en-FI, replaced) |
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