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Monoclonal Gammopathy of Undetermined Significance MeSH Descriptor Data 2022


MeSH Heading
Monoclonal Gammopathy of Undetermined Significance
Tree Number(s)
C15.378.147.542.640
C15.378.147.780.570
C20.683.460.640
C20.683.780.640
Unique ID
D008998
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D008998
Scope Note
Conditions characterized by the presence of M protein (Monoclonal protein) in serum or urine without clinical manifestations of plasma cell dyscrasia.
Entry Term(s)
Benign Monoclonal Gammopathies
Monoclonal Gammapathies, Benign
Monoclonal Gammapathy of Undetermined Significance
Monoclonal Gammopathies, Benign
NLM Classification #
WH 400
Previous Indexing
Blood Protein Disorders (1966-1968)
Hypergammaglobulinemia (1969-1985)
Public MeSH Note
1991; see HYPERGAMMAGLOBULINEMIA 1986-1990
History Note
1991(1986); use HYPERGAMMAGLOBULINEMIA 1986-1990
Date Established
1991/01/01
Date of Entry
1985/02/25
Revision Date
2017/06/20
Monoclonal Gammopathy of Undetermined Significance Preferred
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