loading...| Preferred Name |
Monoclonal Gammopathy of Undetermined Significance |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3996 |
| ALT_DEFINITION |
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. |
| code |
C3996 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C116977 |
| Contributing_Source |
CTEP CTRP |
| DEFINITION |
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. |
| Display_Name |
Monoclonal Gammopathy of Undetermined Significance |
| FULL_SYN |
MGUS Benign Monoclonal Gammopathy Monoclonal Gammopathy Of Undetermined Significance (MGUS) Monoclonal Gammopathy of Unknown Significance |
| ICD-O-3_Code |
9765/1 |
| label |
Monoclonal Gammopathy of Undetermined Significance |
| Legacy_Concept_Name |
Monoclonal_Gammopathy_of_Undetermined_Significance |
| Neoplastic_Status |
Malignant |
| Preferred_Name |
Monoclonal Gammopathy of Undetermined Significance |
| prefixIRI |
C3996 |
| prefLabel |
Monoclonal Gammopathy of Undetermined Significance |
| Semantic_Type |
Neoplastic Process |
| UMLS_CUI |
C0026470 |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/MESH/D008998 | Medical Subject Headings | LOOM |