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... > Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Protein Disorders > Paraproteinemias > Monoclonal Gammopathy of Undetermined Significance > Schnitzler Syndrome
Immune System Diseases > Immunoproliferative Disorders > Paraproteinemias > Monoclonal Gammopathy of Undetermined Significance > Schnitzler Syndrome
Pathological Conditions, Signs and Symptoms > Signs and Symptoms > Hypergammaglobulinemia > Monoclonal Gammopathy of Undetermined Significance > Schnitzler Syndrome
... > Hemic and Lymphatic Diseases > Hematologic Diseases > Blood Protein Disorders > Hypergammaglobulinemia > Monoclonal Gammopathy of Undetermined Significance > Schnitzler Syndrome
Immune System Diseases > Immunoproliferative Disorders > Hypergammaglobulinemia > Monoclonal Gammopathy of Undetermined Significance > Schnitzler Syndrome

Terme préférentiel

Schnitzler Syndrome  

Type

  • mesh:Descriptor

Définition

  • 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.

Concept générique

Qualificatif(s) autorisé(s)

Traductions

URI

http://data.loterre.fr/ark:/67375/JVR-MRQ78NR1-8

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RDF/XML TURTLE JSON-LD Date de création 20/06/1997, dernière modification le 07/08/2001