Skip to main content

Search from vocabulary

Content language

Concept information

Preferred term

Schnitzler Syndrome  

Type

  • Topical Descriptor

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.

History note

  • 98

In other languages

URI

http://www.yso.fi/onto/mesh/D019873

Download this concept:

RDF/XML TURTLE JSON-LD Created 6/20/97, last modified 8/7/01