Preferred Label : schnitzler syndrome;
MeSH definition : 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.;
CISMeF synonym : Schnitzler; schnitzler's syndrome;
Wikipedia link : https://en.wikipedia.org/wiki/Schnitzler syndrome;
Origin ID : D019873;
UMLS CUI : C0524988;
Allowable qualifiers
Currated CISMeF NLP mapping
DO Cross reference
Manual NTBT mappings (CISMeF)
ORDO relation(s)
Record concept(s)
Semantic type(s)
UMLS correspondences (same concept)
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.
https://www.medg.fr/syndrome-de-schnitzler
2019
France
teaching material
scientific and technical information
schnitzler syndrome
Schnitzler syndrome
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http://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=FR&Expert=37748
2011
France
French
schnitzler syndrome
schnitzler syndrome
signs and symptoms
rare diseases
schnitzler syndrome
scientific and technical information
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http://www.orpha.net/data/patho/Pub/fr/Schnitzler-FRfrPub10447v01.pdf
2007
true
France
French
schnitzler syndrome
schnitzler syndrome
schnitzler syndrome
patient education handout
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