Monoclonal Gammopathy of Undetermined Significance D008998

Related MeSH Hierarchy (4)

Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Blood Protein Disorders » Hypergammaglobulinemia » Monoclonal Gammopathy of Undetermined Significance

Diseases [C] » Hemic and Lymphatic Diseases [C15] » Hematologic Diseases » Blood Protein Disorders » Paraproteinemias » Monoclonal Gammopathy of Undetermined Significance

Diseases [C] » Immune System Diseases [C20] » Immunoproliferative Disorders » Hypergammaglobulinemia » Monoclonal Gammopathy of Undetermined Significance

Diseases [C] » Immune System Diseases [C20] » Immunoproliferative Disorders » Paraproteinemias » Monoclonal Gammopathy of Undetermined Significance

Description

Conditions characterized by the presence of M protein (Monoclonal protein) in serum or urine without clinical manifestations of plasma cell dyscrasia.   MeSH

Subtype Terms (1)

Schnitzler Syndrome
6 drugs (3 approved, 3 experimental)



Organization Involved with Phase 4 Indications (1)

Hierarchy Tree View

UMLS Data


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