Structured Summary
Abstract
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.
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35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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98
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References
- National Library of Medicine. Schnitzler Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D019873. http://id.nlm.nih.gov/mesh/2026/D019873
- Schnitzler Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Schnitzler_syndrome
- Schnitzler Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q2259421