01
Diseases
Monoclonal Gammopathy of Undetermined Significance
monoclonal gammopathy of undetermined significance
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 8
Basic Information
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Core Information
- Disease Name
- Monoclonal Gammopathy of Undetermined Significance
- Standard Disease Name
- monoclonal gammopathy of undetermined significance
- MeSH Tree
- No data
- ICD-10
- D47.2
Identifiers
- DO ID
- No data
- MeSH ID
- D008998
- OMIM ID
- No data
- UMLS ID
- C0026470
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_NCI-GLOSS_1602D:A benign condition in which there is a higher-than-normal level of a protein called M protein in the blood. Patients with MGUS are at an increased risk of developing cancer.|NCI2016_02D:A plasma cell disorder in which an abnormal amount of a single immunoglobulin is present in the serum. Up to 25% of cases of monoclonal gammopathy of undetermined significance (MGUS) progress to a B-cell malignancy or myeloma. MGUS may occur in conjunction with various carcinomas, chronic inflammatory and infectious conditions, and other diseases.|MSH2017_2016_08_12: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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