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Schnitzler Syndrome MeSH Descriptor Data 2023


MeSH Heading
Schnitzler Syndrome
Tree Number(s)
C20.683.780.640.700
Unique ID
D019873
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D019873
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.
Public MeSH Note
98
History Note
98
Date Established
1998/01/01
Date of Entry
1997/06/20
Revision Date
2001/08/07
Schnitzler Syndrome Preferred
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