MeSH 搜索器

Schnitzler Syndrome

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.
推出的年份: 1998
副标题
树号: C20.683.780.640.700
MeSH 单一 ID: D019873

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