Preferred Name |
Monoclonal Gammopathy of Undetermined Significance [Disease/Finding] |
|
Synonyms |
Monoclonal Gammapathy of Undetermined Significance Benign Monoclonal Gammopathies |
|
ID |
http://purl.bioontology.org/ontology/NDFRT/N0000002026 |
|
altLabel |
Monoclonal Gammapathy of Undetermined Significance Monoclonal Gammopathy of Undetermined Significance Monoclonal Gammopathies, Benign Monoclonal Gammapathies, Benign Benign Monoclonal Gammopathies |
|
cui |
C0026470 |
|
MESH DEFINITION |
Conditions characterized by the presence of M protein (Monoclonal protein) in serum or urine without clinical manifestations of plasma cell dyscrasia. |
|
MESH DUI |
D008998 |
|
MeSH name |
Monoclonal Gammopathy of Undetermined Significance |
|
MESH UI |
M0014031 |
|
NDFRT kind |
DISEASE_KIND |
|
notation |
N0000002026 |
|
NUI |
N0000002026 |
|
prefLabel |
Monoclonal Gammopathy of Undetermined Significance [Disease/Finding] |
|
SNOMED CID |
58648008 |
|
tui |
T191 |
|
subClassOf |
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