Structured Summary
Abstract
Conditions characterized by the presence of M protein (Monoclonal protein) in serum or urine without clinical manifestations of plasma cell dyscrasia.
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Synonyms
9 entry terms
- Benign Monoclonal Gammopathies
- Monoclonal Gammapathies, Benign
- Monoclonal Gammapathy of Undetermined Significance
- Monoclonal Gammopathies, Benign
- Benign Monoclonal Gammapathies
- Benign Monoclonal Gammapathy
- Benign Monoclonal Gammopathy
- Monoclonal Gammapathy, Benign
- Monoclonal Gammopathy, Benign
MeSH Record
Aspects Covered
35 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
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History Note
1991(1986); use HYPERGAMMAGLOBULINEMIA 1986-1990
MeSH Record
Previous Indexing
- Blood Protein Disorders (1966-1968)
- Hypergammaglobulinemia (1969-1985)
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MeSH Record
NLM Classification
WH 400
AMA Style
References
- National Library of Medicine. Monoclonal Gammopathy of Undetermined Significance. Medical Subject Headings (MeSH). 2026. Unique ID D008998. http://id.nlm.nih.gov/mesh/2026/D008998
- Monoclonal Gammopathy of Undetermined Significance. In: Wikipedia. https://en.wikipedia.org/wiki/Monoclonal_gammopathy_of_undetermined_significance
- Monoclonal Gammopathy of Undetermined Significance. In: Wikidata. https://www.wikidata.org/wiki/Q458138