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Schnitzler Syndrome
Hierarchy: | ∟ ∟ ∟ ∟ ∟ ∟ Schnitzler Syndrome ∟ ∟ ∟ ∟ ∟ ∟ Schnitzler Syndrome ∟ ∟ ∟ ∟ ∟ Schnitzler Syndrome ∟ ∟ ∟ ∟ ∟ Schnitzler Syndrome ∟ ∟ ∟ ∟ ∟ Schnitzler Syndrome X |
Broader terms: | ∟ ∟ ∟ ∟ ∟ ∟ Schnitzler Syndrome ∟ ∟ ∟ ∟ ∟ ∟ Schnitzler Syndrome ∟ ∟ ∟ ∟ ∟ Schnitzler Syndrome ∟ ∟ ∟ ∟ ∟ Schnitzler Syndrome ∟ ∟ ∟ ∟ ∟ Schnitzler Syndrome |
historyNote*: | 98
X |
publicMeSHNote*: | 98
X |
Scope note: | An extremely rare condition manifested as monoclonal IMMUNOGLOBULIN M dysproteinemia without features of lymphoproliferative disease, but with chronic urticaria, fever of unknown origin, disabling bone pain, hyperostosis, and increased erythrocyte sedimentation rate.
X |
activeMeSHYear*: | |
dateCreated*: | 1997-06-20X |
dateEstablished*: | 1998-01-01X |
dateRevised*: | 2001-08-07X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | sjnX |
recordOriginator*: | NDWX |
Type: | |
URI: | |
Labels and equivalent concepts: | Schnitzlerin oireyhtymä (fi) XSchnitzlerin syndrooma (fi, replaced) Schnitzlers syndrom (sv) Syndroma Schnitzler (la-FI, replaced) |
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