Descriptor English: | Schnitzler Syndrome | ||||
Descriptor Spanish: |
Síndrome de Schnitzler
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Descriptor Portuguese: | Síndrome de Schnitzler | ||||
Descriptor French: | Syndrome de Schnitzler | ||||
Tree number(s): |
C20.683.780.640.700 |
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RDF Unique Identifier: | https://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. |
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Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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Public MeSH Note: | 98 |
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History Note: | 98 |
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DeCS ID: | 33364 | ||||
Unique ID: | D019873 | ||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||
Date Established: | 1998/01/01 | ||||
Date of Entry: | 1997/06/20 | ||||
Revision Date: | 2001/08/07 |
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Schnitzler Syndrome
- Preferred
Concept UI |
M0029510 |
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. |
Preferred term | Schnitzler Syndrome |
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