Monoclonal Gammopathy of Undetermined Significance
Conditions characterized by the presence of M protein (Monoclonal protein) in serum or urine without clinical manifestations of plasma cell dyscrasia.
Year introduced: 1991(1986)
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Subheadings:
Tree Number(s): C15.378.147.542.640, C15.378.147.780.570, C20.683.460.640, C20.683.780.640
MeSH Unique ID: D008998
Entry Terms:
- Benign Monoclonal Gammopathies
- Benign Monoclonal Gammopathy
- Monoclonal Gammopathy, Benign
- Monoclonal Gammopathies, Benign
- Monoclonal Gammapathies, Benign
- Benign Monoclonal Gammapathies
- Benign Monoclonal Gammapathy
- Monoclonal Gammapathy, Benign
- Monoclonal Gammapathy of Undetermined Significance
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