| Descriptor English: | Monoclonal Gammopathy of Undetermined Significance | ||||||
| Descriptor Spanish: |
Gammopatía Monoclonal de Relevancia Indeterminada
| ||||||
| Descriptor Portuguese: | Gamopatia Monoclonal de Significância Indeterminada | ||||||
| Descriptor French: | Gammapathie monoclonale de signification indéterminée | ||||||
| Entry term(s): |
Benign Monoclonal Gammapathies Benign Monoclonal Gammapathy Benign Monoclonal Gammopathies Benign Monoclonal Gammopathy Monoclonal Gammapathies, Benign Monoclonal Gammapathy of Undetermined Significance Monoclonal Gammapathy, Benign Monoclonal Gammopathies, Benign Monoclonal Gammopathy, Benign |
||||||
| Tree number(s): |
C15.378.147.542.640 C15.378.147.780.570 C20.683.460.640 C20.683.780.640 |
||||||
| RDF Unique Identifier: | https://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. |
||||||
| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
||||||
| 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 |
||||||
| DeCS ID: | 19566 | ||||||
| Unique ID: | D008998 | ||||||
| NLM Classification: | WH 400 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1991/01/01 | ||||||
| Date of Entry: | 1985/02/25 | ||||||
| Revision Date: | 2017/06/20 |
|
|
Monoclonal Gammopathy of Undetermined Significance
- Preferred
| Concept UI |
M0014031 |
| Scope note | Conditions characterized by the presence of M protein (Monoclonal protein) in serum or urine without clinical manifestations of plasma cell dyscrasia. |
| Preferred term | Monoclonal Gammopathy of Undetermined Significance |
| Entry term(s) |
Benign Monoclonal Gammapathies Benign Monoclonal Gammapathy Benign Monoclonal Gammopathies Benign Monoclonal Gammopathy Monoclonal Gammapathies, Benign Monoclonal Gammapathy of Undetermined Significance Monoclonal Gammapathy, Benign Monoclonal Gammopathies, Benign Monoclonal Gammopathy, Benign |
We want your feedback on the new DeCS / MeSH website
We invite you to complete a survey that will take no more than 3 minutes.
Go to survey
